A trichothecene mycotoxin produced by Fusarium to which wheat, barley, maize (corn) and their products are susceptible to contamination.
3alpha,7alpha,15-trihydroxy-12,13-epoxytrichothec-9-en-8-one
3alpha,7alpha,15-trihydroxy-12,13-epoxytrichothec-9-en-8-one
4-Deoxynivalenol
4-Desoxynivalenol
DON
Dehydronivalenol
Desoxynivalenol
Vomitoxin
deoxynivalenol
3alpha,7alpha,15-trihydroxy-12,13-epoxytrichothec-9-en-8-one
IUPAC
3alpha,7alpha,15-trihydroxy-12,13-epoxytrichothec-9-en-8-one
ChemIDplus
4-Deoxynivalenol
ChemIDplus
4-Desoxynivalenol
ChemIDplus
DON
KEGG_COMPOUND
Dehydronivalenol
ChemIDplus
Desoxynivalenol
ChemIDplus
Vomitoxin
KEGG_COMPOUND
A carotenol that exhibits antioxidant activity. It has been isolated from fruits such as papaya and oranges.
(3R)-beta,beta-caroten-3-ol
beta-Cryptoxanthin
beta-cryptoxanthin
cryptoxanthin
beta-cryptoxanthin
(3R)-beta,beta-caroten-3-ol
IUPAC
beta-Cryptoxanthin
KEGG_COMPOUND
beta-cryptoxanthin
UniProt
cryptoxanthin
ChemIDplus
A naphthol carrying a hydroxy group at position 2.
2-Naphthol
2-naphthol
naphthalen-2-ol
2-Naftol
2-hydroxynaphthalene
2-naftolo
2-naphthalenol
2-naphtol
Antioxygene BN
Azogen Developer A
C.I. Azoic Coupling Component 1
C.I. Developer 5
Developer A
Developer AMS
Developer BN
Isonaphthol
beta-Naftol
beta-Naphthol
beta-Naphtol
beta-hydroxynaphthalene
beta-naftolo
beta-naphthol
beta-naphthyl alcohol
beta-naphthyl hydroxide
2-naphthol
2-Naphthol
KEGG_COMPOUND
2-naphthol
UniProt
naphthalen-2-ol
IUPAC
2-Naftol
ChemIDplus
2-hydroxynaphthalene
HMDB
2-naftolo
ChemIDplus
2-naphthalenol
NIST_Chemistry_WebBook
2-naphtol
ChemIDplus
Antioxygene BN
HMDB
Azogen Developer A
HMDB
C.I. Azoic Coupling Component 1
ChemIDplus
C.I. Developer 5
ChemIDplus
Developer A
ChemIDplus
Developer AMS
ChemIDplus
Developer BN
ChemIDplus
Isonaphthol
ChemIDplus
beta-Naftol
ChemIDplus
beta-Naphthol
KEGG_COMPOUND
beta-Naphtol
ChemIDplus
beta-hydroxynaphthalene
ChemIDplus
beta-hydroxynaphthalene
NIST_Chemistry_WebBook
beta-naftolo
ChemIDplus
beta-naphthol
NIST_Chemistry_WebBook
beta-naphthyl alcohol
ChemIDplus
beta-naphthyl hydroxide
ChemIDplus
Elementary particle not affected by the strong force having a spin 1/2, a negative elementary charge and a rest mass of 0.000548579903(13) u, or 0.51099906(15) MeV.
electron
Elektron
beta
beta(-)
beta-particle
e
e(-)
e-
negatron
electron
electron
ChEBI
electron
IUPAC
electron
KEGG_COMPOUND
Elektron
ChEBI
beta
IUPAC
beta(-)
ChEBI
beta-particle
IUPAC
e
IUPAC
e(-)
UniProt
e-
KEGG_COMPOUND
negatron
IUPAC
A member of the class of 3-(3,4-substituted-phenyl)-1,1-dimethylureas that is urea in which both of the hydrogens attached to one nitrogen are substituted by methyl groups, and one of the hydrogens attached to the other nitrogen is substituted by a 3,4-dichlorophenyl group.
3-(3,4-dichlorophenyl)-1,1-dimethylurea
diuron
1,1-dimethyl-3-(3,4-dichlorophenyl)urea
1-(3,4-dichlorophenyl)-3,3-dimethylurea
1-(3,4-dichlorophenyl)-3,3-dimethyluree
3-(3,4-Dichlor-phenyl)-1,1-dimethyl-harnstoff
3-(3,4-Dichloro-phenyl)-1,1-dimethyl-urea
DCMU
N'-(3,4-dichlorophenyl)-N,N-dimethylurea
N,N,-dimethyl-N'-(3,4-dichlorophenyl)urea
N-(3,4-dichlorophenyl)-N',N'-dimethylurea
diuron
3-(3,4-dichlorophenyl)-1,1-dimethylurea
IUPAC
diuron
UniProt
1,1-dimethyl-3-(3,4-dichlorophenyl)urea
ChemIDplus
1-(3,4-dichlorophenyl)-3,3-dimethylurea
ChemIDplus
1-(3,4-dichlorophenyl)-3,3-dimethyluree
ChemIDplus
3-(3,4-Dichlor-phenyl)-1,1-dimethyl-harnstoff
ChemIDplus
3-(3,4-Dichloro-phenyl)-1,1-dimethyl-urea
ChEMBL
DCMU
ChEBI
N'-(3,4-dichlorophenyl)-N,N-dimethylurea
ChemIDplus
N,N,-dimethyl-N'-(3,4-dichlorophenyl)urea
ChemIDplus
N-(3,4-dichlorophenyl)-N',N'-dimethylurea
ChemIDplus
Any bacterial metabolite produced during a metabolic reaction in Mycoplasma genitalium.
Mycoplasma genitalium metabolites
Mycoplasma genitalium metabolite
Mycoplasma genitalium metabolites
ChEBI
A carboxylic acid anion resulting from the deprotonation of the carboxy group of a dicarboxylic acid monoester.
dicarboxylic acid monoester(1-)
An unsaturated fatty acid anion obtained by the deprotonation of the carboxy group of any octadecanoid.
anionic octadecanoid
anionic octadecanoids
octadecanoid anions
octadecanoid anion
anionic octadecanoid
ChEBI
anionic octadecanoids
ChEBI
octadecanoid anions
ChEBI
An octadecanoid anion anion obtained by the deprotonation of the carboxy group of any hydroperoxyoctadecadienoic acid.
HPODE anion
HPODE anions
hydroperoxyoctadecadienoate
hydroperoxyoctadecadienoates
HPODE(1-)
HPODE anion
ChEBI
HPODE anions
ChEBI
hydroperoxyoctadecadienoate
ChEBI
hydroperoxyoctadecadienoates
SUBMITTER
A class of carbonyl compound encompassing dicarboxylic acids and any derivatives obtained by substitution of either one or both of the carboxy hydrogens.
dicarboxylic acids and derivatives
dicarboxylic acids and O-substituted derivatives
dicarboxylic acids and derivatives
ChEBI
Any member of the class of benzoquinones that is 1,4-benzoquinone or its C-substituted derivatives.
a quinone
p-benzoquinones
para-benzoquinones
1,4-benzoquinones
a quinone
UniProt
p-benzoquinones
ChEBI
para-benzoquinones
ChEBI
Any trienoic fatty acid containing 18 carbons.
FA 18:3
free fatty acid 18:3
fatty acid 18:3
FA 18:3
ChEBI
free fatty acid 18:3
ChEBI
A reagent that lightens or whitens a substrate through chemical reaction. Bleaching reactions usually involve oxidative or reductive processes that degrade colour systems. Bleaching can occur by destroying one or more of the double bonds in the conjugated chain, by cleaving the conjugated chain, or by oxidation of one of the other moieties in the conjugated chain. Their reactivity results in many bleaches having strong bactericidal, disinfecting, and sterilising properties.
bleaching agent
aspartate
An octadecenoate in which the double bond is at C-9.
octadec-9-enoate
9-octadecenoate
C18:1, n-9(1-)
Delta(9)-octadecenoate
octadec-9-enoate
octadec-9-enoate
IUPAC
9-octadecenoate
ChEBI
C18:1, n-9(1-)
ChEBI
Delta(9)-octadecenoate
ChEBI
An organophosphate oxoanion obtained by the deprotonation of the carboxy and one of the phosphate OH groups as well as protonation of the amino group of glyphosate. It is the major microspecies at pH 7.3 (according to Marvin v 6.2.0.).
glyphosate
glyphosate(1-)
glyphosate
UniProt
A polyunsaturated fatty acid anion obtained by deprotonation of the carboxy group of either alpha- or gamma-linolenic acid.
linolenates
linolenate
linolenates
ChEBI
Any polyunsaturated fatty acid anion carrying one or more hydroperoxy substituents.
a hydroperoxy polyunsaturated fatty acid
hydroperoxy polyunsaturated fatty acid anions
hydroperoxy-polyunsaturated fatty acid anion
hydroperoxy-polyunsaturated fatty acid anions
hydroperoxy polyunsaturated fatty acid anion
a hydroperoxy polyunsaturated fatty acid
UniProt
hydroperoxy polyunsaturated fatty acid anions
ChEBI
hydroperoxy-polyunsaturated fatty acid anion
ChEBI
hydroperoxy-polyunsaturated fatty acid anions
ChEBI
Any member of the class of ureas in which at least one of the nitrogens of the urea moiety is substituted by a phenyl or substituted phenyl group.
phenylureas
Any organic compound having an initial boiling point less than or equal to 250 degreeC (482 degreeF) measured at a standard atmospheric pressure of 101.3 kPa.
VOC
VOCs
volatile organic compounds
volatile organic compound
VOC
ChEBI
VOCs
ChEBI
volatile organic compounds
ChEBI
An alkanesulfonate in which the carbon at position 1 is attached to R, which can represent hydrogens, a carbon chain, or other groups.
alkanesulfonate oxoanions
alkanesulfonates
an alkanesulfonate
alkanesulfonate oxoanion
alkanesulfonate oxoanions
ChEBI
alkanesulfonates
ChEBI
an alkanesulfonate
UniProt
An alcohol where the hydroxy group is attached to a saturated carbon atom adjacent to a double bond (R groups may be H, organyl, etc.).
allylic alcohols
allylic alcohol
allylic alcohols
ChEBI
An allylic alcohol in which the carbon atom that links the double bond to the hydroxy group is also attached to two other carbons (R4,R5 =/= H).
tertiary allylic alcohols
tertiary allylic alcohol
tertiary allylic alcohols
ChEBI
A 5-oxo monocarboxylic acid anion obtained by deprotonation of the carboxy group of any diastereomer of jasmonic acid; major species at pH 7.3.
{3-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl}acetate
a jasmonate
jasmonate anion
jasmonic acid anion
{3-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl}acetate
IUPAC
a jasmonate
UniProt
jasmonate anion
ChEBI
A diol in which the two hydroxy groups are on different carbon atoms, usually but not necessarily adjacent.
glycols
Glykol
glycol
glycols
IUPAC
Glykol
ChEBI
A compound that, on administration, undergoes conversion by biochemical (enzymatic), chemical (possibly following an enzymatic step), or physical (e.g. photochemical) activation processes before becoming the active agent for which it is a pro-agent.
pro-agents
proagent
proagents
pro-agent
pro-agents
ChEBI
proagent
ChEBI
proagents
ChEBI
An atom of an element that exhibits properties that are between those of metals and nonmetals, or that has a mixture of them. The term generally includes boron, silicon, germanium, arsenic, antimony, and tellurium, while carbon, aluminium, selenium, polonium, and astatine are less commonly included.
metalloid
metalloids
metalloid atom
metalloid
ChEBI
metalloids
ChEBI
An organic cation obtained by protonation of the amino group of any tertiary amino compound.
a tertiary amine
tertiary amine(1+)
tertiary ammonium ions
tertiary ammonium ion
a tertiary amine
UniProt
tertiary amine(1+)
ChEBI
tertiary ammonium ions
ChEBI
Any compound that can disrupt the functions of the endocrine (hormone) system
endocrine disrupting chemical
endocrine disrupting chemicals
endocrine disrupting compound
endocrine disrupting compounds
endocrine disruptors
endocrine-disrupting chemical
endocrine-disrupting chemicals
hormonally active agent
hormonally active agents
endocrine disruptor
endocrine disrupting chemical
ChEBI
endocrine disrupting chemicals
ChEBI
endocrine disrupting compound
ChEBI
endocrine disrupting compounds
ChEBI
endocrine disruptors
ChEBI
endocrine-disrupting chemical
ChEBI
endocrine-disrupting chemicals
ChEBI
hormonally active agent
ChEBI
hormonally active agents
ChEBI
A Bronsted acid derived from one or more inorganic compounds. Inorganic acids (also known as mineral acids) form hydrons and conjugate base ions when dissolved in water.
inorganic acids
mineral acid
mineral acids
inorganic acid
inorganic acids
ChEBI
mineral acid
ChEBI
mineral acids
ChEBI
A jasmonate anion resulting from the removal of a proton from the carboxy group of (+)-jasmonic acid; major species at pH 7.3.
{(1S,2S)-3-oxo-2-[(2 Z)-pent-2-en-1-yl]cyclopentyl}acetate
(1S,2S)-jasmonic acid anion
(3S,7S)-jasmonate
(+)-jasmonic acid anion
{(1S,2S)-3-oxo-2-[(2 Z)-pent-2-en-1-yl]cyclopentyl}acetate
IUPAC
(1S,2S)-jasmonic acid anion
ChEBI
(3S,7S)-jasmonate
UniProt
Any main group molecular entity that is gaseous at standard temperature and pressure (STP; 0degreeC and 100 kPa).
gas molecular entities
gaseous molecular entities
gaseous molecular entity
gas molecular entity
gas molecular entities
ChEBI
gaseous molecular entities
ChEBI
gaseous molecular entity
ChEBI
Any carotenoid derivative with a psi-end group.
a carotenoid psi-end group
carotenoid psi-end derivative
a carotenoid psi-end group
UniProt
Any carotenoid derivative with an beta-end group
a carotenoid beta-end derivative
carotenoid beta-end derivative
a carotenoid beta-end derivative
UniProt
A cyclic tetrapyrrole anion that is the carbanion obtained by removal of the acidic proton from position 21 of any chlorophyll. Major species at pH 7.3
a chlorophyll
chlorophyll(1-)
a chlorophyll
UniProt
A cyclic tetrapyrrole anion obtained by removal of the acidic proton from position 21 as well as deprotonation of the carboxy group of any chlorophyllide. Major species at pH 7.3
a chlorophyllide
chlorophyllide(2-)
a chlorophyllide
UniProt
An oxo monocarboxylic acid that is (3-oxocyclopentyl)acetic acid substituted by a (2Z)-pent-2-en-1-yl group at position 2 of the cyclopentane ring.
{(1S,2S)-3-oxo-2-[(2 Z)-pent-2-en-1-yl]cyclopentyl}acetic acid
(1S,2S)-jasmonic acid
(+)-jasmonic acid
{(1S,2S)-3-oxo-2-[(2 Z)-pent-2-en-1-yl]cyclopentyl}acetic acid
IUPAC
(1S,2S)-jasmonic acid
ChEBI
carbamate
Carbamat
Karbamat
carbamate ion
carbamic acid, ion(1-)
carbamate
carbamate
IUPAC
carbamate
UniProt
Carbamat
ChEBI
Karbamat
ChEBI
carbamate ion
ChemIDplus
carbamic acid, ion(1-)
ChemIDplus
A chemical compound that causes a substantial proportion of exposed people or animals to develop an allergic reaction in normal tissue after repeated exposure to the compound.
sensitisers
sensitizer
sensitizers
sensitiser
sensitisers
ChEBI
sensitizer
ChEBI
sensitizers
ChEBI
Any phenol that acts as an electron donor.
a phenolic donor
phenolic donors
phenolic donor
a phenolic donor
UniProt
phenolic donors
ChEBI
An alpha-oxyketone that has a hydroxy group as the alpha-oxy moiety.
alpha-hydroxy ketones
alpha-hydroxy-ketone
alpha-hydroxy-ketones
alpha-hydroxyketone
alpha-hydroxyketones
alpha-hydroxy ketone
alpha-hydroxy ketones
ChEBI
alpha-hydroxy-ketone
ChEBI
alpha-hydroxy-ketones
ChEBI
alpha-hydroxyketone
ChEBI
alpha-hydroxyketones
ChEBI
FA 18:1
FA(18:1)
fatty acid 18:1
FA 18:1
ChEBI
FA(18:1)
ChEBI
FA 18:2
FA(18:2)
fatty acid 18:2
FA 18:2
ChEBI
FA(18:2)
ChEBI
A non-proteinogenic alpha-amino acid that is 2-aminobutanoic acid which is substituted at position 4 by a hydroxy(methyl)phosphoryl group.
2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid
2-amino-4-[hydroxy(methyl)phosphoryl]butyric acid
phosphinothricin
2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid
2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid
IUPAC
2-amino-4-[hydroxy(methyl)phosphoryl]butyric acid
IUPAC
phosphinothricin
ChEBI
A 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid that has S configuration at position 2. A glutamine synthetase inhibitor, it is used (generally as the corresponding ammonium or sodium salts, known as glufosinate-P-ammonium and glufosinate-P-sodium, respectively) as a herbicide to control annual weeds and grasses.
(2S)-2-amino-4-[hydroxy(methyl)phosphinoyl]butyric acid
(2S)-2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid
(+)-glufosinate
(2S)-2-amino-4-(hydroxymethylphosphinyl)butanoic acid
(2S)-glufosinate
(S)-glufosinate
(S)-phosphinothricin
4-[hydroxy(methyl)phosphinoyl]-L-homoalanine
L-glufosinate
phosphinothricin-P
glufosinate-P
(2S)-2-amino-4-[hydroxy(methyl)phosphinoyl]butyric acid
IUPAC
(2S)-2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid
IUPAC
(+)-glufosinate
ChEBI
(2S)-2-amino-4-(hydroxymethylphosphinyl)butanoic acid
Alan_Wood's_Pesticides
(2S)-glufosinate
ChEBI
(S)-glufosinate
ChEBI
(S)-phosphinothricin
ChemIDplus
4-[hydroxy(methyl)phosphinoyl]-L-homoalanine
Alan_Wood's_Pesticides
L-glufosinate
ChEBI
phosphinothricin-P
PPDB
A 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid that has R configuration at position 2. The enantiomer of glufosinate-P.
(2R)-2-amino-4-[hydroxy(methyl)phosphinoyl]butyric acid
(2R)-2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid
(-)-glufosinate
(2R)-2-amino-4-(hydroxymethylphosphinyl)butanoic acid
(R)-glufosinate
4-[hydroxy(methyl)phosphinoyl]-D-homoalanine
D-glufosinate
(2R)-glufosinate
(2R)-2-amino-4-[hydroxy(methyl)phosphinoyl]butyric acid
IUPAC
(2R)-2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid
IUPAC
(-)-glufosinate
ChEBI
(2R)-2-amino-4-(hydroxymethylphosphinyl)butanoic acid
ChEBI
(R)-glufosinate
ChEBI
4-[hydroxy(methyl)phosphinoyl]-D-homoalanine
ChEBI
D-glufosinate
ChEBI
An amino acid zwitterion resulting from the transfer of a proton from the carboxy group to the amino group of (2R)-glufosinate.
(2R)-2-azaniumyl-4-[hydroxy(methyl)phosphoryl]butanoate
(2R)-2-azaniumyl-4-[hydroxy(methyl)phosphoryl]butyrate
(-)-glufosinate zwitterion
(2R)-2-azaniumyl-4-(hydroxymethylphosphinyl)butanoate
(R)-glufosinate zwitterion
4-[hydroxy(methyl)phosphinoyl]-D-homoalanine zwitterion
(2R)-glufosinate zwitterion
(2R)-2-azaniumyl-4-[hydroxy(methyl)phosphoryl]butanoate
IUPAC
(2R)-2-azaniumyl-4-[hydroxy(methyl)phosphoryl]butyrate
IUPAC
(-)-glufosinate zwitterion
ChEBI
(2R)-2-azaniumyl-4-(hydroxymethylphosphinyl)butanoate
ChEBI
(R)-glufosinate zwitterion
ChEBI
4-[hydroxy(methyl)phosphinoyl]-D-homoalanine zwitterion
ChEBI
An amino acid zwitterion resulting from the transfer of a proton from the carboxy group to the amino group of glufosinate-P.
(2S)-2-azaniumyl-4-[hydroxy(methyl)phosphinoyl]butyrate
(2S)-2-azaniumyl-4-[hydroxy(methyl)phosphoryl]butanoate
(+)-glufosinate zwitterion
(2S)-2-amino-4-(hydroxymethylphosphinyl)butanoic acid zwitterion
(2S)-glufosinate zwitterion
(S)-glufosinate zwitterion
4-[hydroxy(methyl)phosphinoyl]-L-homoalanine zwitterion
glufosinate-P zwitterion
(2S)-2-azaniumyl-4-[hydroxy(methyl)phosphinoyl]butyrate
IUPAC
(2S)-2-azaniumyl-4-[hydroxy(methyl)phosphoryl]butanoate
IUPAC
(+)-glufosinate zwitterion
ChEBI
(2S)-2-amino-4-(hydroxymethylphosphinyl)butanoic acid zwitterion
ChEBI
(2S)-glufosinate zwitterion
ChEBI
(S)-glufosinate zwitterion
ChEBI
4-[hydroxy(methyl)phosphinoyl]-L-homoalanine zwitterion
ChEBI
An organic anion resulting from the deprotonation of the phosphinic acid group of (2R)-glufosinate zwitterion.
(2R)-2-azaniumyl-4-(methylphosphinato)butanoate
(2R)-2-azaniumyl-4-(methylphosphinato)butyrate
(-)-glufosinate zwitterion(1-)
(R)-glufosinate zwitterion(1-)
4-(methylphosphinato)-D-homoalanine zwitterion
(2R)-glufosinate zwitterion(1-)
(2R)-2-azaniumyl-4-(methylphosphinato)butanoate
IUPAC
(2R)-2-azaniumyl-4-(methylphosphinato)butyrate
IUPAC
(-)-glufosinate zwitterion(1-)
ChEBI
(R)-glufosinate zwitterion(1-)
ChEBI
4-(methylphosphinato)-D-homoalanine zwitterion
ChEBI
An organic anion resulting from the deprotonation of the phosphinic acid group of (2R)-glufosinate-P zwitterion.
(2S)-2-azaniumyl-4-[hydroxy(methyl)phosphinato]butanoate
(2S)-2-azaniumyl-4-[hydroxy(methyl)phosphinato]butyrate
(+)-glufosinate zwitterion(1-)
(2S)-2-amino-4-(hydroxymethylphosphinato)butanoic acid zwitterion
(2S)-glufosinate zwitterion(1-)
(S)-glufosinate zwitterion(1-)
4-[hydroxy(methyl)phosphinoyl]-L-homoalanine zwitterion(1-)
glufosinate-P zwitterion(1-)
(2S)-2-azaniumyl-4-[hydroxy(methyl)phosphinato]butanoate
IUPAC
(2S)-2-azaniumyl-4-[hydroxy(methyl)phosphinato]butyrate
IUPAC
(+)-glufosinate zwitterion(1-)
ChEBI
(2S)-2-amino-4-(hydroxymethylphosphinato)butanoic acid zwitterion
ChEBI
(2S)-glufosinate zwitterion(1-)
ChEBI
(S)-glufosinate zwitterion(1-)
ChEBI
4-[hydroxy(methyl)phosphinoyl]-L-homoalanine zwitterion(1-)
ChEBI
An alpha-amino-acid anion that is the conjugate base of glutamic acid, having anionic carboxy groups and a cationic amino group
glutamate(1-)
hydrogen glutamate
2-ammoniopentanedioate
glutamate
glutamic acid monoanion
glutamate(1-)
glutamate(1-)
JCBN
hydrogen glutamate
IUPAC
2-ammoniopentanedioate
IUPAC
glutamate
UniProt
glutamic acid monoanion
JCBN
9-hydroperoxy-(10E,12Z)-octadecadienoate
9-hydroperoxy-(10E,12Z)-octadecadienoate(1-)
9-HPODE(1-)
9-hydroperoxy-(10E,12Z)-octadecadienoate
UniProt
9-hydroperoxy-(10E,12Z)-octadecadienoate(1-)
SUBMITTER
Any agent that induces nausea and vomiting.
emetics
emetic
emetics
ChEBI
A molecular entity that can transfer an electron to another molecular entity.
electron donor
Elektronendonator
donneur d'electron
electron donor
electron donor
IUPAC
Elektronendonator
ChEBI
donneur d'electron
IUPAC
A purine nucleobase found in humans and other organisms.
xanthine
2,6-dioxopurine
2,6-dioxopurines
xanthines
xanthine
xanthine
ChEBI
2,6-dioxopurine
ChEBI
2,6-dioxopurines
ChEBI
xanthines
ChEBI
A molecular entity that can accept an electron, a pair of electrons, an atom or a group from another molecular entity.
Acceptor
A
Akzeptor
Hydrogen-acceptor
Oxidized donor
accepteur
acceptor
Acceptor
KEGG_COMPOUND
A
KEGG_COMPOUND
Akzeptor
ChEBI
Hydrogen-acceptor
KEGG_COMPOUND
Oxidized donor
KEGG_COMPOUND
accepteur
ChEBI
A sulfur-containing amino acid that is propanoic acid with an amino group at position 2 and a sulfanyl group at position 3.
Cysteine
cysteine
2-Amino-3-mercaptopropionic acid
2-amino-3-mercaptopropanoic acid
2-amino-3-sulfanylpropanoic acid
C
Cys
Cystein
Hcys
Zystein
cisteina
cysteine
Cysteine
KEGG_COMPOUND
cysteine
ChEBI
cysteine
IUPAC
2-Amino-3-mercaptopropionic acid
KEGG_COMPOUND
2-amino-3-mercaptopropanoic acid
JCBN
2-amino-3-sulfanylpropanoic acid
IUPAC
C
ChEBI
Cys
ChEBI
Cystein
ChEBI
Hcys
IUPAC
Zystein
ChEBI
cisteina
ChEBI
A simple monocarboxylic acid containing two carbons.
ACETIC ACID
Acetic acid
acetic acid
AcOH
CH3-COOH
CH3CO2H
E 260
E-260
E260
Essigsaeure
Ethanoic acid
Ethylic acid
HOAc
INS No. 260
MeCO2H
MeCOOH
Methanecarboxylic acid
acide acetique
ethoic acid
acetic acid
ACETIC ACID
PDBeChem
Acetic acid
KEGG_COMPOUND
acetic acid
IUPAC
AcOH
ChEBI
CH3-COOH
IUPAC
CH3CO2H
ChEBI
E 260
ChEBI
E-260
ChEBI
E260
ChEBI
Essigsaeure
ChEBI
Ethanoic acid
KEGG_COMPOUND
Ethylic acid
ChemIDplus
HOAc
ChEBI
INS No. 260
ChEBI
MeCO2H
ChEBI
MeCOOH
ChEBI
Methanecarboxylic acid
ChemIDplus
acide acetique
ChemIDplus
ethoic acid
ChEBI
A large group of antibiotics isolated from various species of Streptomyces and characterised by having a substituted phenoxazine ring linked to two cyclic heterodetic peptides.
Actinomycin
actinomycins
actinomycin
Actinomycin
KEGG_COMPOUND
actinomycins
ChEBI
An oxygen hydride consisting of an oxygen atom that is covalently bonded to two hydrogen atoms
WATER
Water
oxidane
water
BOUND WATER
H2O
HOH
Wasser
[OH2]
acqua
agua
aqua
dihydridooxygen
dihydrogen oxide
eau
hydrogen hydroxide
water
WATER
PDBeChem
Water
KEGG_COMPOUND
oxidane
IUPAC
water
IUPAC
BOUND WATER
PDBeChem
H2O
KEGG_COMPOUND
H2O
UniProt
HOH
ChEBI
Wasser
ChEBI
[OH2]
IUPAC
acqua
ChEBI
agua
ChEBI
aqua
ChEBI
dihydridooxygen
IUPAC
dihydrogen oxide
IUPAC
eau
ChEBI
hydrogen hydroxide
ChEBI
The general name for the hydrogen nucleus, to be used without regard to the hydrogen nuclear mass (either for hydrogen in its natural abundance or where it is not desired to distinguish between the isotopes).
Hydron
hydrogen(1+)
hydron
H(+)
H+
hydron
Hydron
KEGG_COMPOUND
hydrogen(1+)
IUPAC
hydron
IUPAC
H(+)
UniProt
H+
KEGG_COMPOUND
The simplest (and the only achiral) proteinogenic amino acid, with a hydrogen atom as its side chain.
GLYCINE
Glycine
aminoacetic acid
glycine
Aminoacetic acid
Aminoessigsaeure
G
Gly
Glycin
Glycocoll
Glykokoll
Glyzin
H2N-CH2-COOH
Hgly
Leimzucker
aminoethanoic acid
glycine
GLYCINE
PDBeChem
Glycine
KEGG_COMPOUND
aminoacetic acid
IUPAC
glycine
IUPAC
Aminoacetic acid
KEGG_COMPOUND
Aminoessigsaeure
ChEBI
G
ChEBI
Gly
KEGG_COMPOUND
Glycin
ChemIDplus
Glycocoll
ChemIDplus
Glykokoll
ChEBI
Glyzin
ChEBI
H2N-CH2-COOH
IUPAC
Hgly
IUPAC
Leimzucker
ChemIDplus
aminoethanoic acid
ChEBI
aminoethanoic acid
JCBN
A monocarboxylic acid anion that is the conjugate base of 1-naphthaleneacetic acid, arising from the deprotonation of the carboxy group; major species at pH 7.3.
1-naphthaleneacetate
naphthalen-1-ylacetate
(naphthalen-1-yl)acetate
1-naphthylacetate
naphthalene-1-acetate
1-naphthaleneacetate
1-naphthaleneacetate
UniProt
naphthalen-1-ylacetate
IUPAC
(naphthalen-1-yl)acetate
IUPAC
1-naphthylacetate
ChEBI
naphthalene-1-acetate
ChEBI
Aldehydic parent sugars (polyhydroxy aldehydes H[CH(OH)]nC(=O)H, n >= 2) and their intramolecular hemiacetals.
Aldose
aldoses
an aldose
aldose
Aldose
KEGG_COMPOUND
aldoses
ChEBI
an aldose
UniProt
Any alpha-amino acid having L-configuration at the alpha-carbon.
L-alpha-amino acid
L-alpha-amino acids
L-2-Amino acid
L-Amino acid
L-alpha-amino acids
L-alpha-amino acid
L-alpha-amino acid
IUPAC
L-alpha-amino acids
IUPAC
L-2-Amino acid
KEGG_COMPOUND
L-Amino acid
KEGG_COMPOUND
L-alpha-amino acids
ChEBI
A primary alcohol is a compound in which a hydroxy group, -OH, is attached to a saturated carbon atom which has either three hydrogen atoms attached to it or only one other carbon atom and two hydrogen atoms attached to it.
Primary alcohol
1-Alcohol
a primary alcohol
primary alcohols
primary alcohol
Primary alcohol
KEGG_COMPOUND
1-Alcohol
KEGG_COMPOUND
a primary alcohol
UniProt
primary alcohols
ChEBI
A monocarboxylic acid anion that is the conjugate base of formic acid. Induces severe metabolic acidosis and ocular injury in human subjects.
formate
HCO2 anion
aminate
formiate
formic acid, ion(1-)
formylate
hydrogen carboxylate
methanoate
formate
formate
IUPAC
formate
UniProt
HCO2 anion
NIST_Chemistry_WebBook
aminate
ChEBI
formiate
ChEBI
formic acid, ion(1-)
ChemIDplus
formylate
ChEBI
hydrogen carboxylate
ChEBI
methanoate
ChEBI
A member of the class of phenylureas that is urea in which one of the nitrogens is substituted by two methyl groups while the other is substituted by a phenyl group which carries two unspecified groups at positions 3 and 4 of the phenyl ring.
3-(3,4-substituted-phenyl)-1,1-dimethylureas
N'-(3,4-substituted-phenyl)-N,N-dimethylurea
N'-(3,4-substituted-phenyl)-N,N-dimethylureas
a 1,1-dimethyl-3-phenylurea
3-(3,4-substituted-phenyl)-1,1-dimethylurea
3-(3,4-substituted-phenyl)-1,1-dimethylureas
ChEBI
N'-(3,4-substituted-phenyl)-N,N-dimethylurea
ChEBI
N'-(3,4-substituted-phenyl)-N,N-dimethylureas
ChEBI
a 1,1-dimethyl-3-phenylurea
UniProt
Any N-acyl-amino acid in which the amino acid moiety has D configuration.
N-acyl-D-amino acid
A peptide containing ten or more amino acid residues.
Polypeptide
polypeptides
Polypeptid
polipeptido
polypeptide
Polypeptide
KEGG_COMPOUND
polypeptides
IUPAC
Polypeptid
ChEBI
polipeptido
ChEBI
A tetrahydroxyflavone in which the four hydroxy groups are located at positions 3', 4', 5 and 7. It is thought to play an important role in the human body as an antioxidant, a free radical scavenger, an anti-inflammatory agent and an immune system modulator as well as being active against several cancers.
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one
Luteolin
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-benzopyrone
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one
3',4',5,7-Tetrahydroxyflavone
5,7,3',4'-Tetrahydroxyflavone
Luteolol
Salifazide
digitoflavone
flacitran
luteolin
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one
IUPAC
Luteolin
KEGG_COMPOUND
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-benzopyrone
ChemIDplus
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one
ChemIDplus
3',4',5,7-Tetrahydroxyflavone
KEGG_COMPOUND
5,7,3',4'-Tetrahydroxyflavone
KEGG_COMPOUND
Luteolol
ChemIDplus
Salifazide
ChemIDplus
digitoflavone
ChEBI
flacitran
ChEBI
A fatty acid with a chain length ranging from C13 to C22.
Long-chain fatty acid
Higher fatty acid
LCFA
LCFAs
long-chain fatty acids
long-chain fatty acid
Long-chain fatty acid
KEGG_COMPOUND
Higher fatty acid
KEGG_COMPOUND
LCFA
ChEBI
LCFAs
ChEBI
long-chain fatty acids
ChEBI
A jasmonate ester that is the methyl ester of jasmonic acid.
(-)-Methyl jasmonate
methyl {(1R,2R)-3-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl}acetate
3-oxo-2-(2-pentenyl)cyclopentaneacetic acid methyl ester
Methyl jasmonate
methyl (-)-jasmonate
(-)-methyl jasmonate
(-)-Methyl jasmonate
KEGG_COMPOUND
methyl {(1R,2R)-3-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl}acetate
IUPAC
3-oxo-2-(2-pentenyl)cyclopentaneacetic acid methyl ester
ChEBI
Methyl jasmonate
KEGG_COMPOUND
methyl (-)-jasmonate
ChEBI
methyl (-)-jasmonate
UniProt
An acyclic carotene commonly obtained from tomatoes and other red fruits.
LYCOPENE
Lycopene
psi,psi-carotene
(6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,24,26,30-tridecaene
all-trans-lycopene
lycopene
LYCOPENE
PDBeChem
Lycopene
KEGG_COMPOUND
psi,psi-carotene
IUPAC
(6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,24,26,30-tridecaene
ChEBI
all-trans-lycopene
ChemIDplus
all-trans-lycopene
UniProt
An optically active form of glutamic acid having D-configuration.
(2R)-2-aminopentanedioic acid
D-Glutamic acid
D-glutamic acid
(R)-2-aminopentanedioic acid
D-2-Aminoglutaric acid
D-Glutaminic acid
D-Glutaminsaeure
DGL
glutamic acid D-form
D-glutamic acid
(2R)-2-aminopentanedioic acid
IUPAC
D-Glutamic acid
KEGG_COMPOUND
D-glutamic acid
IUPAC
(R)-2-aminopentanedioic acid
ChEBI
D-2-Aminoglutaric acid
KEGG_COMPOUND
D-Glutaminic acid
KEGG_COMPOUND
D-Glutaminsaeure
ChEBI
DGL
PDBeChem
glutamic acid D-form
ChemIDplus
A nucleobase-containing molecular entity with a polymeric structure comprised of a linear sequence of 13 or more nucleotide residues.
Polynucleotide
polynucleotides
polynucleotide
Polynucleotide
KEGG_COMPOUND
polynucleotides
ChEBI
An optically active form of glutamic acid having L-configuration.
(2S)-2-aminopentanedioic acid
L-Glutamic acid
L-glutamic acid
(S)-2-aminopentanedioic acid
(S)-glutamic acid
E
GLUTAMIC ACID
Glu
Glutamate
L-Glu
L-Glutaminic acid
L-Glutaminsaeure
acide glutamique
acido glutamico
acidum glutamicum
glutamic acid
L-glutamic acid
(2S)-2-aminopentanedioic acid
IUPAC
L-Glutamic acid
KEGG_COMPOUND
L-glutamic acid
IUPAC
(S)-2-aminopentanedioic acid
ChEBI
(S)-glutamic acid
NIST_Chemistry_WebBook
E
ChEBI
GLUTAMIC ACID
PDBeChem
Glu
ChEBI
Glutamate
KEGG_COMPOUND
L-Glu
ChEBI
L-Glutaminic acid
KEGG_COMPOUND
L-Glutaminsaeure
ChEBI
acide glutamique
ChEBI
acido glutamico
ChEBI
acidum glutamicum
ChEBI
glutamic acid
ChEBI
A monoatomic monoanion resulting from the addition of an electron to any halogen atom.
halide ions
HX
Halide
a halide anion
halide anions
halide(1-)
halides
halogen anion
halide anion
halide ions
IUPAC
HX
KEGG_COMPOUND
Halide
KEGG_COMPOUND
a halide anion
UniProt
halide anions
ChEBI
halide(1-)
ChEBI
halides
ChEBI
halogen anion
ChEBI
An azane that consists of a single nitrogen atom covelently bonded to three hydrogen atoms.
AMMONIA
Ammonia
ammonia
azane
Ammoniak
NH3
R-717
[NH3]
ammoniac
amoniaco
spirit of hartshorn
ammonia
AMMONIA
PDBeChem
Ammonia
KEGG_COMPOUND
ammonia
IUPAC
azane
IUPAC
Ammoniak
ChemIDplus
NH3
IUPAC
NH3
KEGG_COMPOUND
NH3
UniProt
R-717
ChEBI
[NH3]
MolBase
ammoniac
ChEBI
amoniaco
ChEBI
spirit of hartshorn
ChemIDplus
The simplest member of the class of benzoates that is the conjugate base of benzoic acid, comprising a benzoic acid core with a proton missing to give a charge of -1.
benzoate
Benzenecarboxylate
Benzeneformate
Benzenemethanoate
Phenylcarboxylate
Phenylformate
benzoate anion
benzoic acid, ion(1-)
benzoate
benzoate
IUPAC
benzoate
UniProt
Benzenecarboxylate
HMDB
Benzeneformate
HMDB
Benzenemethanoate
HMDB
Phenylcarboxylate
HMDB
Phenylformate
HMDB
benzoate anion
NIST_Chemistry_WebBook
benzoic acid, ion(1-)
ChemIDplus
A sulfur oxoanion obtained by deprotonation of both OH groups of sulfuric acid.
Sulfate
sulfate
tetraoxidosulfate(2-)
tetraoxosulfate(2-)
tetraoxosulfate(VI)
SO4(2-)
SULFATE ION
Sulfate anion(2-)
Sulfate dianion
Sulfate(2-)
Sulfuric acid ion(2-)
[SO4](2-)
sulphate
sulphate ion
sulfate
Sulfate
KEGG_COMPOUND
sulfate
IUPAC
sulfate
UniProt
tetraoxidosulfate(2-)
IUPAC
tetraoxosulfate(2-)
IUPAC
tetraoxosulfate(VI)
IUPAC
SO4(2-)
IUPAC
SULFATE ION
PDBeChem
Sulfate anion(2-)
HMDB
Sulfate dianion
HMDB
Sulfate(2-)
HMDB
Sulfuric acid ion(2-)
HMDB
[SO4](2-)
IUPAC
sulphate
ChEBI
sulphate ion
ChEBI
An octadec-9-enoic acid in which the double bond at C-9 has Z (cis) stereochemistry.
(9Z)-octadec-9-enoic acid
OLEIC ACID
Oleic acid
(9Z)-Octadecenoic acid
(Z)-Octadec-9-enoic acid
18:1 n-9
18:1Delta9cis
C18:1 n-9
FA 18:1
Octadec-9-enoic acid
Oelsaeure
Oleate
cis-9-octadecenoic acid
cis-Delta(9)-octadecenoic acid
cis-oleic acid
oleic acid
(9Z)-octadec-9-enoic acid
IUPAC
OLEIC ACID
PDBeChem
Oleic acid
KEGG_COMPOUND
(9Z)-Octadecenoic acid
KEGG_COMPOUND
(Z)-Octadec-9-enoic acid
KEGG_COMPOUND
18:1 n-9
ChEBI
18:1Delta9cis
ChEBI
C18:1 n-9
ChEBI
FA 18:1
ChEBI
Octadec-9-enoic acid
ChEMBL
Oelsaeure
ChEBI
Oleate
KEGG_COMPOUND
cis-9-octadecenoic acid
NIST_Chemistry_WebBook
cis-Delta(9)-octadecenoic acid
ChemIDplus
cis-oleic acid
ChEBI
A carbonyl group with two C-bound amine groups. The commercially available fertilizer has an analysis of 46-0-0 (N-P2O5-K2O).
UREA
Urea
urea
1728
Carbamide
E927b
H2NC(O)NH2
Harnstoff
Karbamid
carbamide
carbonyldiamide
ur
uree
urea
UREA
PDBeChem
Urea
KEGG_COMPOUND
urea
IUPAC
urea
UniProt
1728
PPDB
Carbamide
KEGG_COMPOUND
E927b
ChEBI
H2NC(O)NH2
ChEBI
Harnstoff
NIST_Chemistry_WebBook
Karbamid
ChEBI
carbamide
ChEBI
carbonyldiamide
NIST_Chemistry_WebBook
ur
IUPAC
uree
ChEBI
A divalent inorganic anion obtained by removal of both protons from phosphonic acid
hydridotrioxidophosphate(2-)
hydridotrioxophosphate(2-)
PHO3(2-)
PHOSPHONATE
Phosphonate
[PHO3](2-)
phosphonate
phosphonate(2-)
hydridotrioxidophosphate(2-)
IUPAC
hydridotrioxophosphate(2-)
IUPAC
PHO3(2-)
IUPAC
PHOSPHONATE
PDBeChem
Phosphonate
KEGG_COMPOUND
[PHO3](2-)
IUPAC
phosphonate
IUPAC
phosphonate
UniProt
hydridooxygenate(1-)
hydroxide
oxidanide
HO-
HYDROXIDE ION
Hydroxide ion
OH(-)
OH-
hydroxide
hydridooxygenate(1-)
IUPAC
hydroxide
IUPAC
oxidanide
IUPAC
HO-
KEGG_COMPOUND
HYDROXIDE ION
PDBeChem
Hydroxide ion
KEGG_COMPOUND
OH(-)
IUPAC
OH-
KEGG_COMPOUND
A 2-aminopurine carrying a 6-oxo substituent.
2-amino-1,9-dihydro-6H-purin-6-one
GUANINE
Guanine
guanine
2-Amino-6-hydroxypurine
2-amino-6-oxopurine
G
Gua
guanine
2-amino-1,9-dihydro-6H-purin-6-one
IUPAC
GUANINE
PDBeChem
Guanine
KEGG_COMPOUND
guanine
UniProt
2-Amino-6-hydroxypurine
KEGG_COMPOUND
2-amino-6-oxopurine
ChEBI
G
ChEBI
Gua
CBN
An inorganic peroxide consisting of two hydroxy groups joined by a covalent oxygen-oxygen single bond.
HYDROGEN PEROXIDE
Hydrogen peroxide
bis(hydridooxygen)(O--O)
dihydrogen peroxide
dihydrogen(peroxide)
dioxidane
hydrogen peroxide
H2O2
HOOH
Oxydol
[OH(OH)]
dihydrogen dioxide
perhydrol
hydrogen peroxide
HYDROGEN PEROXIDE
PDBeChem
Hydrogen peroxide
KEGG_COMPOUND
bis(hydridooxygen)(O--O)
IUPAC
dihydrogen peroxide
IUPAC
dihydrogen(peroxide)
IUPAC
dioxidane
IUPAC
hydrogen peroxide
IUPAC
H2O2
KEGG_COMPOUND
H2O2
UniProt
HOOH
IUPAC
Oxydol
KEGG_COMPOUND
[OH(OH)]
MolBase
dihydrogen dioxide
IUPAC
perhydrol
MetaCyc
Any organic cation that is an aglycon of anthocyanin cation; they are oxygenated derivatives of flavylium (2-phenylchromenylium).
anthocyanidins
Anthocyanidin
anthocyanidin cations
anthocyanidin cation
anthocyanidins
IUPAC
Anthocyanidin
KEGG_COMPOUND
anthocyanidin cations
ChEBI
Compounds having the structure RSR (R =/= H). Such compounds were once called thioethers.
sulfides
RSR
Sulfide
Thioether
organic sulfides
thioethers
organic sulfide
sulfides
IUPAC
RSR
IUPAC
Sulfide
KEGG_COMPOUND
Thioether
KEGG_COMPOUND
organic sulfides
ChEBI
thioethers
IUPAC
A monocarboxylic acid that is acetic acid in which one of the methyl hydrogens has been replaced by a 1H-indol-3-yl group.
1H-indol-3-ylacetic acid
Indole-3-acetic acid
(Indol-3-yl)acetate
(indol-3-yl)acetic acid
2-(indol-3-yl)ethanoic acid
3-Indolylessigsaeure
IAA
IES
Indoleacetic acid
heteroauxin
indole-3-acetic acid
1H-indol-3-ylacetic acid
IUPAC
Indole-3-acetic acid
KEGG_COMPOUND
(Indol-3-yl)acetate
KEGG_COMPOUND
(indol-3-yl)acetic acid
UniProt
2-(indol-3-yl)ethanoic acid
ChEBI
3-Indolylessigsaeure
ChEBI
IAA
KEGG_COMPOUND
IAA
NIST_Chemistry_WebBook
IES
ChEBI
Indoleacetic acid
KEGG_COMPOUND
heteroauxin
NIST_Chemistry_WebBook
An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.
2-aminopropanoic acid
Alanine
alanine
2-Aminopropanoic acid
2-Aminopropionic acid
A
ALA
Alanin
alanina
alanine
2-aminopropanoic acid
IUPAC
Alanine
KEGG_COMPOUND
alanine
IUPAC
2-Aminopropanoic acid
KEGG_COMPOUND
2-Aminopropionic acid
KEGG_COMPOUND
A
ChEBI
ALA
ChEBI
Alanin
ChEBI
alanina
ChEBI
An aromatic hydrocarbon comprising two fused benzene rings. It occurs in the essential oils of numerous plant species e.g. magnolia.
NAPHTHALENE
Naphthalene
naphthalene
Naphthalen
Naphthalin
naftaleno
naftalina
naphtalene
naphtaline
naphthalene
NAPHTHALENE
PDBeChem
Naphthalene
KEGG_COMPOUND
naphthalene
IUPAC
naphthalene
UniProt
Naphthalen
ChEBI
Naphthalin
NIST_Chemistry_WebBook
naftaleno
ChEBI
naftalina
ChEBI
naphtalene
ChEBI
naphtaline
ChEBI
The simplest member of the class of 1,4-benzoquinones, obtained by the formal oxidation of hydroquinone to the corresponding diketone. It is a metabolite of benzene.
1,4-Benzoquinone
1,4-benzoquinone
cyclohexa-2,5-diene-1,4-dione
1,4-Benzochinon
2,5-Cyclohexadiene-1,4-dione
Quinone
benzo-1,4-quinone
benzoquinone
p-Benzoquinone
p-Chinon
p-quinone
para-benzoquinone
1,4-benzoquinone
1,4-Benzoquinone
KEGG_COMPOUND
1,4-benzoquinone
NIST_Chemistry_WebBook
1,4-benzoquinone
UniProt
cyclohexa-2,5-diene-1,4-dione
IUPAC
1,4-Benzochinon
ChEBI
2,5-Cyclohexadiene-1,4-dione
KEGG_COMPOUND
Quinone
KEGG_COMPOUND
benzo-1,4-quinone
NIST_Chemistry_WebBook
benzoquinone
ChemIDplus
p-Benzoquinone
KEGG_COMPOUND
p-Chinon
NIST_Chemistry_WebBook
p-quinone
HMDB
para-benzoquinone
HMDB
A one-carbon compound with formula CO2 in which the carbon is attached to each oxygen atom by a double bond. A colourless, odourless gas under normal conditions, it is produced during respiration by all animals, fungi and microorganisms that depend directly or indirectly on living or decaying plants for food.
CARBON DIOXIDE
Carbon dioxide
carbon dioxide
dioxidocarbon
methanedione
CO2
E 290
E-290
E290
R-744
[CO2]
carbonic anhydride
carbon dioxide
CARBON DIOXIDE
PDBeChem
Carbon dioxide
KEGG_COMPOUND
carbon dioxide
IUPAC
dioxidocarbon
IUPAC
methanedione
IUPAC
CO2
KEGG_COMPOUND
CO2
UniProt
E 290
ChEBI
E-290
ChEBI
E290
ChEBI
R-744
ChEBI
[CO2]
MolBase
carbonic anhydride
UM-BBD
A naturally occurring polypeptide synthesized at the ribosome.
Protein
a protein
polypeptide chain
protein polypeptide chains
protein polypeptide chain
Protein
KEGG_COMPOUND
a protein
UniProt
polypeptide chain
ChEBI
protein polypeptide chains
ChEBI
A trisaccharide composed of alpha-D-galactopyranose, alpha-D-glucopyranose and beta-D-fructofuranose joined in sequence by 1->6 and 1<->2 glycosidic linkages, respectively.
Raffinose
beta-D-fructofuranosyl alpha-D-galactopyranosyl-(1->6)-alpha-D-glucopyranoside
raffinose
6G-alpha-D-galactosylsucrose
Gossypose
Melitose
Melitriose
alpha-D-Galp-(1->6)-alpha-D-Glcp-(1<->2)-beta-D-Fruf
alpha-D-galactopyranosyl-(1->6)-alpha-D-glucopyranosyl beta-D-fructofuranoside
rafinose
raflinose
raffinose
Raffinose
KEGG_COMPOUND
beta-D-fructofuranosyl alpha-D-galactopyranosyl-(1->6)-alpha-D-glucopyranoside
IUPAC
raffinose
UniProt
6G-alpha-D-galactosylsucrose
KEGG_COMPOUND
Gossypose
KEGG_COMPOUND
Melitose
KEGG_COMPOUND
Melitriose
KEGG_COMPOUND
alpha-D-Galp-(1->6)-alpha-D-Glcp-(1<->2)-beta-D-Fruf
JCBN
alpha-D-galactopyranosyl-(1->6)-alpha-D-glucopyranosyl beta-D-fructofuranoside
JCBN
rafinose
ChEBI
raflinose
ChEBI
Any member of the class of organooxygen compounds that is a polyhydroxy-aldehyde or -ketone or a lactol resulting from their intramolecular condensation (monosaccharides); substances derived from these by reduction of the carbonyl group (alditols), by oxidation of one or more hydroxy groups to afford the corresponding aldehydes, ketones, or carboxylic acids, or by replacement of one or more hydroxy group(s) by a hydrogen atom; and polymeric products arising by intermolecular acetal formation between two or more such molecules (disaccharides, polysaccharides and oligosaccharides). Carbohydrates contain only carbon, hydrogen and oxygen atoms; prior to any oxidation or reduction, most have the empirical formula Cm(H2O)n. Compounds obtained from carbohydrates by substitution, etc., are known as carbohydrate derivatives and may contain other elements. Cyclitols are generally not regarded as carbohydrates.
carbohydrate
carbohydrates
Kohlenhydrat
Kohlenhydrate
a carbohydrate
carbohidrato
carbohidratos
glucide
glucides
glucido
glucidos
hydrates de carbone
saccharide
saccharides
saccharidum
carbohydrate
carbohydrate
IUPAC
carbohydrates
IUPAC
Kohlenhydrat
ChEBI
Kohlenhydrate
ChEBI
a carbohydrate
UniProt
carbohidrato
IUPAC
carbohidratos
IUPAC
glucide
ChEBI
glucides
ChEBI
glucido
ChEBI
glucidos
ChEBI
hydrates de carbone
ChEBI
saccharide
IUPAC
saccharides
IUPAC
saccharidum
ChEBI
Amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another with formal loss of water. The term is usually applied to structures formed from alpha-amino acids, but it includes those derived from any amino carboxylic acid. X = OH, OR, NH2, NHR, etc.
Peptide
peptides
Peptid
peptido
peptidos
peptide
Peptide
KEGG_COMPOUND
peptides
IUPAC
Peptid
ChEBI
peptido
ChEBI
peptidos
ChEBI
Any octanoid that is derived from jasmonate.
Jasmonate derivatives
The parent compound of the 6-aminopurines, composed of a purine having an amino group at C-6.
9H-purin-6-amine
ADENINE
Adenine
adenine
6-Aminopurine
A
Ade
Adenin
adenine
9H-purin-6-amine
IUPAC
ADENINE
PDBeChem
Adenine
KEGG_COMPOUND
adenine
UniProt
6-Aminopurine
KEGG_COMPOUND
A
ChEBI
Ade
CBN
Adenin
NIST_Chemistry_WebBook
A six-carbon aromatic annulene in which each carbon atom donates one of its two 2p electrons into a delocalised pi system. A toxic, flammable liquid byproduct of coal distillation, it is used as an industrial solvent. Benzene is a carcinogen that also damages bone marrow and the central nervous system.
BENZENE
Benzene
benzene
Benzen
Benzine
Benzol
Bicarburet of hydrogen
Coal naphtha
Mineral naphtha
Phene
Pyrobenzol
Pyrobenzole
[6]annulene
benzole
cyclohexatriene
phenyl hydride
benzene
BENZENE
PDBeChem
Benzene
KEGG_COMPOUND
benzene
ChEBI
benzene
IUPAC
benzene
UniProt
Benzen
IUPAC
Benzine
UM-BBD
Benzol
ChemIDplus
Bicarburet of hydrogen
ChemIDplus
Coal naphtha
ChemIDplus
Mineral naphtha
ChemIDplus
Phene
ChemIDplus
Pyrobenzol
ChemIDplus
Pyrobenzole
ChemIDplus
[6]annulene
NIST_Chemistry_WebBook
benzole
NIST_Chemistry_WebBook
cyclohexatriene
UM-BBD
phenyl hydride
UM-BBD
A mineral that is an inorganic nutrient which must be ingested and absorbed in adequate amounts to satisfy a wide range of essential metabolic and/or structural functions in the human body.
mineral nutrient
mineral nutrients
nutrient mineral
nutrient minerals
mineral nutrient
mineral nutrient
ChEBI
mineral nutrients
ChEBI
nutrient mineral
ChEBI
nutrient minerals
ChEBI
D-alpha-amino acid
D-alpha-amino acids
D-Amino acid
D-alpha-amino acids
D-alpha-amino acid
D-alpha-amino acid
ChEBI
D-alpha-amino acids
IUPAC
D-Amino acid
KEGG_COMPOUND
D-alpha-amino acids
ChEBI
Any oligosaccharide, polysaccharide or their derivatives consisting of monosaccharides or monosaccharide derivatives linked by glycosidic bonds. See also http://www.ontobee.org/ontology/GNO?iri=http://purl.obolibrary.org/obo/GNO_00000001.
glycans
glycan
glycans
ChEBI
An aldehyde resulting from the formal oxidation of methanol.
FORMALDEHYDE
Formaldehyde
formaldehyde
FORMALIN
Formaldehyd
Formalin
Methanal
Methylene oxide
Oxomethane
Oxomethylene
formaldehyde
FORMALDEHYDE
PDBeChem
Formaldehyde
KEGG_COMPOUND
formaldehyde
IUPAC
formaldehyde
UniProt
FORMALIN
ChEMBL
Formaldehyd
NIST_Chemistry_WebBook
Formalin
KEGG_COMPOUND
Methanal
KEGG_COMPOUND
Methylene oxide
KEGG_COMPOUND
Oxomethane
KEGG_COMPOUND
Oxomethylene
KEGG_COMPOUND
The D-enantiomer of mannitol.
D-Mannitol
D-mannitol
(2R,3R,4R,5R)-Hexane-1,2,3,4,5,6-hexaol
(2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexaol
(2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexol
D-(-)-Mannitol
E 421
E-421
E421
Mannitol
Osmitrol
dulcite
manna sugar
mannite
mannitol
D-mannitol
D-Mannitol
KEGG_COMPOUND
D-mannitol
ChEBI
D-mannitol
IUPAC
D-mannitol
UniProt
(2R,3R,4R,5R)-Hexane-1,2,3,4,5,6-hexaol
ChEMBL
(2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexaol
ChEMBL
(2R,3R,4R,5R)-hexane-1,2,3,4,5,6-hexol
ChEMBL
D-(-)-Mannitol
NIST_Chemistry_WebBook
E 421
ChEBI
E-421
ChEBI
E421
ChEBI
Mannitol
KEGG_COMPOUND
Osmitrol
DrugBank
dulcite
ChEBI
manna sugar
ChEBI
mannite
ChEBI
mannitol
ChEMBL
Chlorophyllide a
Chlorophyllid a
chlorophyllide a
Chlorophyllide a
KEGG_COMPOUND
Chlorophyllid a
ChEBI
A monohydroxybenzoic acid that is benzoic acid with a hydroxy group at the ortho position. It is obtained from the bark of the white willow and wintergreen leaves.
2-hydroxybenzoic acid
Salicylic acid
2-HYDROXYBENZOIC ACID
2-carboxyphenol
o-Hydroxybenzoic acid
o-carboxyphenol
o-hydroxybenzoic acid
salicylic acid
2-hydroxybenzoic acid
IUPAC
Salicylic acid
KEGG_COMPOUND
2-HYDROXYBENZOIC ACID
PDBeChem
2-carboxyphenol
NIST_Chemistry_WebBook
o-Hydroxybenzoic acid
KEGG_COMPOUND
o-carboxyphenol
NIST_Chemistry_WebBook
o-hydroxybenzoic acid
NIST_Chemistry_WebBook
A doubly-charged N-acyl-L-alpha-amino acid anion resulting from deprotonation of both carboxy groups of N-acetyl-L-aspartic acid.
(2S)-2-acetamidobutanedioate
(S)-2-(acetylamino)succinate
N-Acetyl-L-aspartate
N-acetyl-L-aspartate
N-acetyl-L-aspartate(2-)
(2S)-2-acetamidobutanedioate
IUPAC
(S)-2-(acetylamino)succinate
ChEBI
N-Acetyl-L-aspartate
KEGG_COMPOUND
N-acetyl-L-aspartate
UniProt
High molecular weight, linear polymers, composed of nucleotides containing deoxyribose and linked by phosphodiester bonds; DNA contain the genetic information of organisms.
Deoxyribonucleic acid
deoxyribonucleic acids
(Deoxyribonucleotide)m
(Deoxyribonucleotide)n
(Deoxyribonucleotide)n+m
DNA
DNAn
DNAn+1
DNS
Desoxyribonukleinsaeure
deoxyribonucleic acids
desoxyribose nucleic acid
thymus nucleic acid
deoxyribonucleic acid
Deoxyribonucleic acid
KEGG_COMPOUND
deoxyribonucleic acids
IUPAC
(Deoxyribonucleotide)m
KEGG_COMPOUND
(Deoxyribonucleotide)n
KEGG_COMPOUND
(Deoxyribonucleotide)n+m
KEGG_COMPOUND
DNA
IUPAC
DNA
KEGG_COMPOUND
DNA
UniProt
DNAn
KEGG_COMPOUND
DNAn+1
KEGG_COMPOUND
DNS
ChEBI
Desoxyribonukleinsaeure
ChEBI
deoxyribonucleic acids
ChEBI
desoxyribose nucleic acid
ChemIDplus
thymus nucleic acid
ChEBI
The D-enantiomer of phenylalanine.
(2R)-2-amino-3-phenylpropanoic acid
D-PHENYLALANINE
D-Phenylalanine
D-phenylalanine
D-Phe
D-alpha-Amino-beta-phenylpropionic acid
DPN
phenylalanine D-form
D-phenylalanine
(2R)-2-amino-3-phenylpropanoic acid
IUPAC
D-PHENYLALANINE
PDBeChem
D-Phenylalanine
KEGG_COMPOUND
D-phenylalanine
IUPAC
D-Phe
ChEBI
D-alpha-Amino-beta-phenylpropionic acid
KEGG_COMPOUND
DPN
PDBeChem
phenylalanine D-form
ChemIDplus
Fluoride
fluoride
fluoride(1-)
F(-)
F-
FLUORIDE ION
Fluoride ion
Fluorine anion
fluoride
Fluoride
KEGG_COMPOUND
fluoride
IUPAC
fluoride
UniProt
fluoride(1-)
IUPAC
F(-)
IUPAC
F-
KEGG_COMPOUND
FLUORIDE ION
PDBeChem
Fluoride ion
KEGG_COMPOUND
Fluorine anion
NIST_Chemistry_WebBook
The L-enantiomer of aspartic acid.
(2S)-2-aminobutanedioic acid
L-Aspartic acid
L-aspartic acid
(S)-2-aminobutanedioic acid
(S)-2-aminosuccinic acid
2-Aminosuccinic acid
ASPARTIC ACID
Asp
D
L-Asparaginsaeure
L-aspartic acid
(2S)-2-aminobutanedioic acid
IUPAC
L-Aspartic acid
KEGG_COMPOUND
L-aspartic acid
IUPAC
(S)-2-aminobutanedioic acid
ChEBI
(S)-2-aminosuccinic acid
ChEBI
2-Aminosuccinic acid
KEGG_COMPOUND
ASPARTIC ACID
PDBeChem
Asp
ChEBI
D
ChEBI
L-Asparaginsaeure
ChEBI
A compound in which a carbonyl group is bonded to two carbon atoms: R2C=O (neither R may be H).
Ketone
ketones
Keton
R-CO-R'
a ketone
cetone
ketones
ketone
Ketone
KEGG_COMPOUND
ketones
IUPAC
Keton
ChEBI
R-CO-R'
KEGG_COMPOUND
a ketone
UniProt
cetone
ChEBI
ketones
ChEBI
A compound in which one or more of the OH groups of phosphoric acid have been replaced with an amino or substituted amino group. The term is commonly confined to the phosphoric triamides, P(=O)(NR2)3, since replacement of one or two OH groups produces phosphoramidic acids: P(=O)(OH)(NR2)2 , P(=O)(OH)2(NR2).
phosphamide
phosphamides
phosphoramides
phosphoramide
phosphoramides
ChEBI
phosphamide
ChEBI
phosphamides
ChEBI
hydrogen(trioxidosulfate)(1-)
hydrogensulfite(1-)
hydrogentrioxosulfate(1-)
hydrogentrioxosulfate(IV)
hydroxidodioxidosulfate(1-)
monohydrogentrioxosulfate
Bisulfite
HSO3(-)
HSO3-
Hydrogen sulfite
[SO2(OH)](-)
bisulfite
bisulphite
hydrogen sulfite(1-)
hydrosulfite anion
hydrogensulfite
hydrogen(trioxidosulfate)(1-)
IUPAC
hydrogensulfite(1-)
IUPAC
hydrogentrioxosulfate(1-)
IUPAC
hydrogentrioxosulfate(IV)
IUPAC
hydroxidodioxidosulfate(1-)
IUPAC
monohydrogentrioxosulfate
IUPAC
Bisulfite
KEGG_COMPOUND
HSO3(-)
IUPAC
HSO3-
KEGG_COMPOUND
Hydrogen sulfite
KEGG_COMPOUND
[SO2(OH)](-)
IUPAC
bisulfite
ChemIDplus
bisulphite
ChemIDplus
hydrogen sulfite(1-)
ChemIDplus
hydrosulfite anion
ChemIDplus
An aldohexose used as a source of energy and metabolic intermediate.
Glucose
gluco-hexose
glucose
DL-glucose
Glc
Glukose
glucose
Glucose
KEGG_COMPOUND
gluco-hexose
IUPAC
glucose
IUPAC
DL-glucose
ChEBI
Glc
JCBN
Glukose
ChEBI
A hydroxyether which contains both an ether and alcohol functional groups. It is one of the most versatile classes of organic solvents which are commonly used in paints, cleaners, adhesives, pharmaceuticals and cosmetics.
glycol ethers
glycol ether
glycol ethers
ChEBI
The 7H-tautomer of purine.
7H-purine
Purine
Purine base
7H-purine
7H-purine
IUPAC
Purine
KEGG_COMPOUND
Purine base
KEGG_COMPOUND
The conjugate base of propionic acid; a key precursor in lipid biosynthesis.
propanoate
propionate
CH3-CH2-COO(-)
EtCO2 anion
carboxylatoethane
ethanecarboxylate
ethylformate
metacetonate
methylacetate
propanate
propanoate
propanoic acid, ion(1-)
pseudoacetate
propionate
propanoate
IUPAC
propionate
IUPAC
CH3-CH2-COO(-)
IUPAC
EtCO2 anion
NIST_Chemistry_WebBook
carboxylatoethane
ChEBI
ethanecarboxylate
ChEBI
ethylformate
ChEBI
metacetonate
ChEBI
methylacetate
ChEBI
propanate
ChEBI
propanoate
UniProt
propanoic acid, ion(1-)
ChemIDplus
pseudoacetate
ChEBI
The L-enantiomer of phenylalanine.
(2S)-2-amino-3-phenylpropanoic acid
L-Phenylalanine
L-phenylalanine
(S)-2-Amino-3-phenylpropionic acid
(S)-alpha-Amino-beta-phenylpropionic acid
3-phenyl-L-alanine
F
PHENYLALANINE
Phe
beta-phenyl-L-alanine
L-phenylalanine
(2S)-2-amino-3-phenylpropanoic acid
IUPAC
L-Phenylalanine
KEGG_COMPOUND
L-phenylalanine
IUPAC
(S)-2-Amino-3-phenylpropionic acid
HMDB
(S)-alpha-Amino-beta-phenylpropionic acid
KEGG_COMPOUND
3-phenyl-L-alanine
NIST_Chemistry_WebBook
F
ChEBI
PHENYLALANINE
PDBeChem
Phe
ChEBI
beta-phenyl-L-alanine
NIST_Chemistry_WebBook
Any substance that inhibits the process of ferroptosis (a type of programmed cell death dependent on iron and characterized by the accumulation of lipid peroxides) in organisms.
ferroptosis inhibitors
ferroptosis inhibitor
ferroptosis inhibitors
ChEBI
Any substance that induces or promotes ferroptosis (a type of programmed cell death dependent on iron and characterized by the accumulation of lipid peroxides) in organisms.
ferroptosis inducers
ferroptosis inducer
ferroptosis inducers
ChEBI
An octadecadienoic acid in which the two double bonds are at positions 9 and 12 and have Z (cis) stereochemistry.
(9Z,12Z)-octadeca-9,12-dienoic acid
LINOLEIC ACID
Linoleic acid
(9Z,12Z)-Octadecadienoic acid
(Z,Z)-9,12-octadecadienoic acid
9-cis,12-cis-Octadecadienoic acid
9Z,12Z-octadecadienoic acid
C18:2 9c, 12c omega6 todos cis-9,12-octadienoico
C18:2, n-6,9 all-cis
LA
acide cis-linoleique
acide linoleique
acido linoleico
all-cis-9,12-octadecadienoic acid
cis,cis-9,12-octadecadienoic acid
cis,cis-linoleic acid
cis-Delta(9,12)-octadecadienoic acid
linolic acid
linoleic acid
(9Z,12Z)-octadeca-9,12-dienoic acid
IUPAC
LINOLEIC ACID
PDBeChem
Linoleic acid
KEGG_COMPOUND
(9Z,12Z)-Octadecadienoic acid
KEGG_COMPOUND
(Z,Z)-9,12-octadecadienoic acid
NIST_Chemistry_WebBook
9-cis,12-cis-Octadecadienoic acid
KEGG_COMPOUND
9Z,12Z-octadecadienoic acid
LIPID_MAPS
C18:2 9c, 12c omega6 todos cis-9,12-octadienoico
ChEBI
C18:2, n-6,9 all-cis
ChEBI
LA
ChEBI
acide cis-linoleique
ChEBI
acide linoleique
ChEBI
acido linoleico
ChEBI
all-cis-9,12-octadecadienoic acid
ChEBI
cis,cis-9,12-octadecadienoic acid
ChEBI
cis,cis-linoleic acid
ChEBI
cis,cis-linoleic acid
NIST_Chemistry_WebBook
cis-Delta(9,12)-octadecadienoic acid
ChemIDplus
linolic acid
ChEBI
A sulfur oxoanion that is the conjugate base of hydrogen sulfite (H2SO3).
sulfite
trioxidosulfate(2-)
trioxosulfate(2-)
trioxosulfate(IV)
SO3
SO3(2-)
SULFITE ION
[SO3](2-)
sulphite
sulfite
sulfite
IUPAC
sulfite
UniProt
trioxidosulfate(2-)
IUPAC
trioxosulfate(2-)
IUPAC
trioxosulfate(IV)
IUPAC
SO3
ChEBI
SO3(2-)
IUPAC
SULFITE ION
PDBeChem
[SO3](2-)
IUPAC
sulphite
ChEBI
The D-enantiomer of aspartic acid.
(2R)-2-aminobutanedioic acid
D-Aspartic acid
D-aspartic acid
(R)-2-aminobutanedioic acid
(R)-2-aminosuccinic acid
D-Asparaginsaeure
DAS
aspartic acid D-form
D-aspartic acid
(2R)-2-aminobutanedioic acid
IUPAC
D-Aspartic acid
KEGG_COMPOUND
D-aspartic acid
IUPAC
(R)-2-aminobutanedioic acid
ChEBI
(R)-2-aminosuccinic acid
ChEBI
D-Asparaginsaeure
ChEBI
DAS
PDBeChem
aspartic acid D-form
ChemIDplus
A straight-chain saturated fatty acid containing five carbon atoms.
Valeric acid
pentanoic acid
1-butanecarboxylic acid
CH3-[CH2]3-COOH
PENTANOIC ACID
Pentanoate
Pentanoic acid
Valerate
Valerianic acid
Valeriansaeure
n-BuCOOH
n-Pentanoate
n-Valeric acid
n-pentanoic acid
n-valeric acid
pentoic acid
propylacetic acid
valeric acid, normal
valeric acid
Valeric acid
KEGG_COMPOUND
pentanoic acid
IUPAC
1-butanecarboxylic acid
ChemIDplus
1-butanecarboxylic acid
NIST_Chemistry_WebBook
CH3-[CH2]3-COOH
IUPAC
PENTANOIC ACID
PDBeChem
Pentanoate
KEGG_COMPOUND
Pentanoic acid
KEGG_COMPOUND
Valerate
KEGG_COMPOUND
Valerianic acid
KEGG_COMPOUND
Valeriansaeure
ChEBI
n-BuCOOH
ChEBI
n-Pentanoate
KEGG_COMPOUND
n-Valeric acid
KEGG_COMPOUND
n-pentanoic acid
ChemIDplus
n-valeric acid
ChemIDplus
pentoic acid
ChEBI
propylacetic acid
ChemIDplus
valeric acid, normal
ChemIDplus
A compound RC(=O)H, in which a carbonyl group is bonded to one hydrogen atom and to one R group.
Aldehyde
aldehyde
aldehydes
Aldehyd
RC(=O)H
RCHO
aldehido
aldehidos
aldehydes
aldehydum
an aldehyde
aldehyde
Aldehyde
KEGG_COMPOUND
aldehyde
ChEBI
aldehyde
IUPAC
aldehydes
IUPAC
Aldehyd
ChEBI
RC(=O)H
IUPAC
RCHO
KEGG_COMPOUND
aldehido
ChEBI
aldehidos
ChEBI
aldehydes
ChEBI
aldehydum
ChEBI
an aldehyde
UniProt
A 2-hydroxy monocarboxylic acid that is acetic acid where the methyl group has been hydroxylated.
GLYCOLIC ACID
Glycolic acid
hydroxyacetic acid
2-Hydroxyacetic acid
2-Hydroxyethanoic acid
Glycollic acid
HOCH2COOH
Hydroxyacetic acid
Hydroxyethanoic acid
alpha-Hydroxyacetic acid
alpha-hydroxyacetic acid
glycolic acid
GLYCOLIC ACID
PDBeChem
Glycolic acid
KEGG_COMPOUND
hydroxyacetic acid
IUPAC
2-Hydroxyacetic acid
ChemIDplus
2-Hydroxyethanoic acid
NIST_Chemistry_WebBook
Glycollic acid
ChemIDplus
HOCH2COOH
NIST_Chemistry_WebBook
Hydroxyacetic acid
KEGG_COMPOUND
Hydroxyethanoic acid
ChemIDplus
alpha-Hydroxyacetic acid
HMDB
alpha-hydroxyacetic acid
NIST_Chemistry_WebBook
A pseudohalide anion that is the conjugate base of hydrogen cyanide.
Cyanide
cyanide
nitridocarbonate(1-)
CN(-)
CN-
CYANIDE ION
Prussiate
Zyanid
cyanide
Cyanide
ChEBI
Cyanide
KEGG_COMPOUND
cyanide
IUPAC
nitridocarbonate(1-)
IUPAC
CN(-)
IUPAC
CN-
KEGG_COMPOUND
CYANIDE ION
PDBeChem
Prussiate
KEGG_COMPOUND
Zyanid
ChEBI
A carbohydrate that is an acyclic polyol having the general formula HOCH2[CH(OH)]nCH2OH (formally derivable from an aldose by reduction of the carbonyl group).
Alditol
alditol
Glycitol
Sugar alcohol
alditols
alditol
Alditol
KEGG_COMPOUND
alditol
UniProt
Glycitol
KEGG_COMPOUND
Sugar alcohol
KEGG_COMPOUND
alditols
ChEBI
The carbon oxoanion resulting from the removal of a proton from carbonic acid.
Hydrogencarbonate
hydrogen(trioxidocarbonate)(1-)
hydrogencarbonate
hydrogencarbonate(1-)
hydrogentrioxocarbonate(1-)
hydrogentrioxocarbonate(IV)
hydroxidodioxidocarbonate(1-)
Acid carbonate
BICARBONATE ION
Bicarbonate
HCO3(-)
HCO3-
[CO2(OH)](-)
hydrogen carbonate
hydrogencarbonate
Hydrogencarbonate
KEGG_COMPOUND
hydrogen(trioxidocarbonate)(1-)
IUPAC
hydrogencarbonate
IUPAC
hydrogencarbonate
UniProt
hydrogencarbonate(1-)
IUPAC
hydrogentrioxocarbonate(1-)
IUPAC
hydrogentrioxocarbonate(IV)
IUPAC
hydroxidodioxidocarbonate(1-)
IUPAC
Acid carbonate
KEGG_COMPOUND
BICARBONATE ION
PDBeChem
Bicarbonate
KEGG_COMPOUND
HCO3(-)
IUPAC
HCO3-
KEGG_COMPOUND
[CO2(OH)](-)
IUPAC
hydrogen carbonate
PDBeChem
A common and naturally occurring pyrimidine nucleobase in which the pyrimidine ring is substituted with two oxo groups at positions 2 and 4. Found in RNA, it base pairs with adenine and replaces thymine during DNA transcription.
URACIL
Uracil
pyrimidine-2,4(1H,3H)-dione
uracil
2,4(1H,3H)-pyrimidinedione
2,4-Dioxopyrimidine
2,4-Pyrimidinedione
U
Ura
Urazil
uracil
URACIL
PDBeChem
Uracil
KEGG_COMPOUND
pyrimidine-2,4(1H,3H)-dione
IUPAC
uracil
UniProt
2,4(1H,3H)-pyrimidinedione
NIST_Chemistry_WebBook
2,4-Dioxopyrimidine
HMDB
2,4-Pyrimidinedione
HMDB
U
ChEBI
Ura
CBN
Urazil
ChEBI
The simplest member of the class toluenes consisting of a benzene core which bears a single methyl substituent.
TOLUENE
Toluene
toluene
Toluen
Toluol
methylbenzene
phenylmethane
toluene
TOLUENE
PDBeChem
Toluene
KEGG_COMPOUND
toluene
ChEBI
toluene
IUPAC
toluene
UniProt
Toluen
NIST_Chemistry_WebBook
Toluol
NIST_Chemistry_WebBook
methylbenzene
PDBeChem
phenylmethane
ChemIDplus
A cyclic carotene obtained by dimerisation of all-trans-retinol. A strongly-coloured red-orange pigment abundant in plants and fruit and the most active and important provitamin A carotenoid.
BETA-CAROTENE
beta,beta-carotene
beta-Carotene
1,1'-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaene-1,18-diyl]bis(2,6,6-trimethylcyclohexene)
all-trans-beta-carotene
beta-Karotin
beta-carotene
BETA-CAROTENE
PDBeChem
beta,beta-carotene
IUPAC
beta-Carotene
KEGG_COMPOUND
1,1'-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaene-1,18-diyl]bis(2,6,6-trimethylcyclohexene)
ChEBI
all-trans-beta-carotene
NIST_Chemistry_WebBook
all-trans-beta-carotene
UniProt
beta-Karotin
ChEBI
A benzenediol comprising benzene core carrying two hydroxy substituents para to each other.
Hydroquinone
benzene-1,4-diol
hydroquinone
1,4-Benzenediol
1,4-Dihydroxybenzene
4-Hydroxyphenol
Benzene-1,4-diol
Eldoquin
Quinol
p-Benzenediol
p-Hydroquinone
p-hydroxyphenol
hydroquinone
Hydroquinone
KEGG_COMPOUND
benzene-1,4-diol
IUPAC
hydroquinone
UniProt
1,4-Benzenediol
KEGG_COMPOUND
1,4-Dihydroxybenzene
KEGG_COMPOUND
4-Hydroxyphenol
KEGG_COMPOUND
Benzene-1,4-diol
KEGG_COMPOUND
Eldoquin
ChemIDplus
Quinol
KEGG_COMPOUND
p-Benzenediol
KEGG_COMPOUND
p-Hydroquinone
KEGG_COMPOUND
p-hydroxyphenol
NIST_Chemistry_WebBook
A ferulic acid consisting of trans-cinnamic acid bearing methoxy and hydroxy substituents at positions 3 and 4 respectively on the phenyl ring.
(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic acid
Ferulic acid
(E)-3-(4-Hydroxy-3-methoxyphenyl)-2-propenoic acid
(E)-4'-hydroxy-3'-methoxycinnamic acid
(E)-4-Hydroxy-3-methoxycinnamic acid
(E)-Ferulic acid
3-(4-Hydroxy-3-methoxyphenyl)propenoic acid
3-methoxy-4-hydroxy-trans-cinnamic acid
4-Hydroxy-3-methoxycinnamic acid
4-hydroxy-3-methoxycinnamic acid
trans-4-Hydroxy-3-methoxycinnamic acid
trans-Ferulic acid
ferulic acid
(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic acid
IUPAC
Ferulic acid
KEGG_COMPOUND
(E)-3-(4-Hydroxy-3-methoxyphenyl)-2-propenoic acid
NIST_Chemistry_WebBook
(E)-4'-hydroxy-3'-methoxycinnamic acid
NIST_Chemistry_WebBook
(E)-4-Hydroxy-3-methoxycinnamic acid
HMDB
(E)-Ferulic acid
ChemIDplus
3-(4-Hydroxy-3-methoxyphenyl)propenoic acid
NIST_Chemistry_WebBook
3-methoxy-4-hydroxy-trans-cinnamic acid
ChEBI
4-Hydroxy-3-methoxycinnamic acid
KEGG_COMPOUND
4-hydroxy-3-methoxycinnamic acid
ChEBI
trans-4-Hydroxy-3-methoxycinnamic acid
ChemIDplus
trans-Ferulic acid
ChemIDplus
A nitrogen oxoanion formed by loss of a proton from nitric acid. Principal species present at pH 7.3.
nitrate
trioxidonitrate(1-)
trioxonitrate(1-)
trioxonitrate(V)
NITRATE ION
NO3
NO3(-)
[NO3](-)
nitrate(1-)
nitrate
nitrate
IUPAC
nitrate
UniProt
trioxidonitrate(1-)
IUPAC
trioxonitrate(1-)
IUPAC
trioxonitrate(V)
IUPAC
NITRATE ION
PDBeChem
NO3
ChEBI
NO3(-)
IUPAC
[NO3](-)
IUPAC
nitrate(1-)
ChemIDplus
Any compound that supports healthy aging, slows the biological aging process, or extends lifespan.
anti-aging agent
anti-aging agents
anti-aging drug
anti-aging drugs
geroprotective agent
geroprotective agents
geroprotectors
geroprotector
anti-aging agent
ChEBI
anti-aging agents
ChEBI
anti-aging drug
ChEBI
anti-aging drugs
ChEBI
geroprotective agent
ChEBI
geroprotective agents
ChEBI
geroprotectors
ChEBI
Any B-vitamin that exhibits biological activity against vitamin B9 deficiency. Vitamin B9 refers to the many forms of folic acid and its derivatives, including tetrahydrofolic acid (the active form), methyltetrahydrofolate (the primary form found in blood), methenyltetrahydrofolate, folinic acid amongst others. They are present in abundance in green leafy vegetables, citrus fruits, and animal products. Lack of vitamin B9 leads to anemia, a condition in which the body cannot produce sufficient number of red blood cells. Symptoms of vitamin B9 deficiency include fatigue, muscle weakness, and pale skin.
vitamin B9
folate vitamer
folate vitamers
vitamin B-9
vitamin B9 vitamer
vitamin B9 vitamers
vitamins B9
vitamin B9
vitamin B9
ChEBI
folate vitamer
ChEBI
folate vitamers
ChEBI
vitamin B-9
ChEBI
vitamin B9 vitamer
ChEBI
vitamin B9 vitamers
ChEBI
vitamins B9
ChEBI
Benzenediol
benzenediol
dihydroxybenzene
benzenediol
Benzenediol
KEGG_COMPOUND
benzenediol
IUPAC
dihydroxybenzene
ChEBI
A triol with a structure of propane substituted at positions 1, 2 and 3 by hydroxy groups.
GLYCEROL
Glycerol
glycerol
propane-1,2,3-triol
1,2,3-Propanetriol
1,2,3-Trihydroxypropane
Glycerin
Glyceritol
Glyzerin
Gro
Oelsuess
Propanetriol
Trihydroxypropane
glycerine
glycerol
glycerolum
glycyl alcohol
glycerol
GLYCEROL
PDBeChem
Glycerol
KEGG_COMPOUND
glycerol
ChEBI
glycerol
UniProt
propane-1,2,3-triol
IUPAC
1,2,3-Propanetriol
KEGG_COMPOUND
1,2,3-Trihydroxypropane
KEGG_COMPOUND
Glycerin
KEGG_COMPOUND
Glyceritol
HMDB
Glyzerin
ChEBI
Gro
JCBN
Oelsuess
ChEBI
Propanetriol
HMDB
Trihydroxypropane
HMDB
glycerine
ChEBI
glycerol
ChemIDplus
glycerolum
ChemIDplus
glycyl alcohol
NIST_Chemistry_WebBook
The primary alcohol that is the simplest aliphatic alcohol, comprising a methyl and an alcohol group.
METHANOL
Methanol
methanol
CH3OH
MeOH
Methyl alcohol
Methylalkohol
carbinol
spirit of wood
wood alcohol
wood naphtha
wood spirit
methanol
METHANOL
PDBeChem
Methanol
KEGG_COMPOUND
methanol
IUPAC
methanol
UniProt
CH3OH
ChEBI
MeOH
ChEBI
Methyl alcohol
KEGG_COMPOUND
Methylalkohol
NIST_Chemistry_WebBook
carbinol
ChemIDplus
spirit of wood
HMDB
wood alcohol
ChemIDplus
wood naphtha
ChemIDplus
wood spirit
NIST_Chemistry_WebBook
A compound containing at least one carbon-halogen bond (where X is a halogen atom).
RX
organic halide
organic halides
organohalogen compounds
organohalogen compound
RX
KEGG_COMPOUND
RX
UniProt
organic halide
KEGG_COMPOUND
organic halides
ChEBI
organohalogen compounds
ChEBI
Any glyceride resulting from the condensation of all three hydroxy groups of glycerol (propane-1,2,3-triol) with fatty acids.
Triglyceride
triglycerides
Triacylglycerol
Triglycerid
Triglyzerid
a triacylglycerol
triacylglycerols
triglycerides
triglyceride
Triglyceride
KEGG_COMPOUND
triglycerides
IUPAC
Triacylglycerol
KEGG_COMPOUND
Triglycerid
ChEBI
Triglyzerid
ChEBI
a triacylglycerol
UniProt
triacylglycerols
LIPID_MAPS
triglycerides
ChEBI
A mononuclear parent hydride consisting of covalently bonded hydrogen and chlorine atoms.
Hydrogen chloride
chlorane
chloridohydrogen
hydrogen chloride
Chlorwasserstoff
HCl
Hydrochloride
Hydrogenchlorid
Wasserstoffchlorid
[HCl]
chlorure d'hydrogene
cloruro de hidrogeno
hydrochloric acid
hydrogen chloride
Hydrogen chloride
KEGG_COMPOUND
chlorane
IUPAC
chloridohydrogen
IUPAC
hydrogen chloride
IUPAC
Chlorwasserstoff
ChEBI
HCl
KEGG_COMPOUND
Hydrochloride
KEGG_COMPOUND
Hydrogenchlorid
ChEBI
Wasserstoffchlorid
ChEBI
[HCl]
IUPAC
chlorure d'hydrogene
ChEBI
cloruro de hidrogeno
ChEBI
hydrochloric acid
ChemIDplus
A molecular entity that can transfer ("donate") an electron, a pair of electrons, an atom or a group to another molecular entity.
Donor
Donator
donneur
donor
Donor
KEGG_COMPOUND
Donator
ChEBI
donneur
ChEBI
A carbamate ester obtained by the formal condensation of ethanol with carbamic acid. It has been found in alcoholic beverages.
Urethane
ethyl carbamate
urethane
Ethyl carbamate
carbamic acid ethyl ester
urethane
Urethane
KEGG_COMPOUND
ethyl carbamate
IUPAC
urethane
UniProt
Ethyl carbamate
KEGG_COMPOUND
carbamic acid ethyl ester
ChEBI
A glycosyl glycoside formed by glucose and fructose units joined by an acetal oxygen bridge from hemiacetal of glucose to the hemiketal of the fructose.
SUCROSE
Sucrose
beta-D-fructofuranosyl alpha-D-glucopyranoside
sucrose
1-alpha-D-Glucopyranosyl-2-beta-D-fructofuranoside
Cane sugar
Saccharose
Sacharose
White sugar
beta-D-Fruf-(2<->1)-alpha-D-Glcp
sacarosa
table sugar
sucrose
SUCROSE
PDBeChem
Sucrose
KEGG_COMPOUND
beta-D-fructofuranosyl alpha-D-glucopyranoside
IUPAC
sucrose
UniProt
1-alpha-D-Glucopyranosyl-2-beta-D-fructofuranoside
KEGG_COMPOUND
Cane sugar
KEGG_COMPOUND
Saccharose
KEGG_COMPOUND
Sacharose
ChEBI
White sugar
HMDB
beta-D-Fruf-(2<->1)-alpha-D-Glcp
JCBN
sacarosa
ChEBI
table sugar
ChemIDplus
A halide anion formed when chlorine picks up an electron to form an an anion.
Chloride
chloride
chloride(1-)
CHLORIDE ION
Chloride ion
Chloride(1-)
Chlorine anion
Cl(-)
Cl-
chloride
Chloride
KEGG_COMPOUND
chloride
IUPAC
chloride
UniProt
chloride(1-)
IUPAC
CHLORIDE ION
PDBeChem
Chloride ion
KEGG_COMPOUND
Chloride(1-)
ChemIDplus
Chlorine anion
NIST_Chemistry_WebBook
Cl(-)
IUPAC
Cl-
KEGG_COMPOUND
'Lipids' is a loosely defined term for substances of biological origin that are soluble in nonpolar solvents. They consist of saponifiable lipids, such as glycerides (fats and oils) and phospholipids, as well as nonsaponifiable lipids, principally steroids.
Lipid
lipids
lipid
Lipid
KEGG_COMPOUND
lipids
IUPAC
A class of terpenoids formed in plants in response to fungal infection, physical damage, chemical injury, or a pathogenic process.
terpenoid phytoalexins
terpenoid phytoalexin
terpenoid phytoalexins
ChEBI
Any six-carbon monosaccharide which in its linear form contains either an aldehyde group at position 1 (aldohexose) or a ketone group at position 2 (ketohexose).
Hexose
WURCS=2.0/1,1,0/[axxxxh-1x_1-5_2*NCC/3=O]/1/
hexoses
hexose
Hexose
KEGG_COMPOUND
WURCS=2.0/1,1,0/[axxxxh-1x_1-5_2*NCC/3=O]/1/
GlyTouCan
hexoses
ChEBI
hydrogen halide
hydrogen halides
HX
hydrogen halides
hydrogen halide
hydrogen halide
IUPAC
hydrogen halides
IUPAC
HX
UniProt
hydrogen halides
ChEBI
ethene
Aethen
Aethylen
CH2=CH2
Ethylene
H2C=CH2
R-1150
ethene
ethene
IUPAC
ethene
UniProt
Aethen
ChEBI
Aethylen
ChEBI
CH2=CH2
IUPAC
Ethylene
KEGG_COMPOUND
H2C=CH2
ChEBI
R-1150
ChEBI
A biomacromolecule consisting of large numbers of monosaccharide residues linked glycosidically. This term is commonly used only for those containing more than ten monosaccharide residues.
Polysaccharide
polysaccharides
Glycan
Glycane
Glykan
Glykane
glycans
polisacarido
polisacaridos
polysaccharide
Polysaccharide
KEGG_COMPOUND
polysaccharides
IUPAC
Glycan
KEGG_COMPOUND
Glycane
ChEBI
Glykan
ChEBI
Glykane
ChEBI
glycans
IUPAC
polisacarido
ChEBI
polisacaridos
IUPAC
CHLOROPHYLL A
Chlorophyll a
[(2E,7R,11R)-3,7,11,15-tetramethylhexadec-2-en-1-yl (2(2)R,17S,18S)-7-ethyl-2(1),2(2),17,18-tetrahydro-2(2)-(methoxycarbonyl)-3,8,13,17-tetramethyl-2(1)-oxo-12-ethenylcyclopenta[at]porphyrin-18-propanoato(2-)]magnesium
(SP-4-2)-((2E,7R,11R)-3,7,11,15-tetramethyl-2-hexadecenyl (3S,4S,21R)-9-ethenyl-14-ethyl-21-(methoxycarbonyl)-4,8,13,18-tetramethyl-20-oxo-3-phorbinepropanoato(2-)-kappaN(23),kappaN(24),kappaN(25),kappaN(26))-magnesium
Chlorophyll
chlorophyll a
CHLOROPHYLL A
PDBeChem
Chlorophyll a
KEGG_COMPOUND
[(2E,7R,11R)-3,7,11,15-tetramethylhexadec-2-en-1-yl (2(2)R,17S,18S)-7-ethyl-2(1),2(2),17,18-tetrahydro-2(2)-(methoxycarbonyl)-3,8,13,17-tetramethyl-2(1)-oxo-12-ethenylcyclopenta[at]porphyrin-18-propanoato(2-)]magnesium
IUPAC
(SP-4-2)-((2E,7R,11R)-3,7,11,15-tetramethyl-2-hexadecenyl (3S,4S,21R)-9-ethenyl-14-ethyl-21-(methoxycarbonyl)-4,8,13,18-tetramethyl-20-oxo-3-phorbinepropanoato(2-)-kappaN(23),kappaN(24),kappaN(25),kappaN(26))-magnesium
ChemIDplus
Chlorophyll
ChemIDplus
An alpha-amino acid that is glutaric acid bearing a single amino substituent at position 2.
2-aminopentanedioic acid
Glutamic acid
glutamic acid
2-Aminoglutaric acid
DL-Glutamic acid
DL-Glutaminic acid
E
Glu
Glutamate
Glutaminic acid
Glutaminsaeure
glutamic acid
2-aminopentanedioic acid
IUPAC
Glutamic acid
KEGG_COMPOUND
glutamic acid
IUPAC
2-Aminoglutaric acid
KEGG_COMPOUND
DL-Glutamic acid
KEGG_DRUG
DL-Glutaminic acid
KEGG_COMPOUND
E
ChEBI
Glu
ChEBI
Glutamate
KEGG_COMPOUND
Glutaminic acid
KEGG_COMPOUND
Glutaminsaeure
ChEBI
A beta-D-glucan in which the glucose units are connected by (1->4) linkages.
(1->4)-beta-D-glucopyranan
(1,4-beta-D-Glucosyl)n
(1,4-beta-D-Glucosyl)n+1
(1,4-beta-D-Glucosyl)n-1
(1,4-beta-D-glucosyl)n
1,4-beta-D-Glucan
Cellulose
(1->4)-beta-D-glucan
(1->4)-beta-D-glucopyranan
IUPAC
(1,4-beta-D-Glucosyl)n
KEGG_COMPOUND
(1,4-beta-D-Glucosyl)n+1
KEGG_COMPOUND
(1,4-beta-D-Glucosyl)n-1
KEGG_COMPOUND
(1,4-beta-D-glucosyl)n
IUBMB
(1,4-beta-D-glucosyl)n
UniProt
1,4-beta-D-Glucan
KEGG_COMPOUND
Cellulose
KEGG_COMPOUND
An iron group element atom that has atomic number 26.
iron
26Fe
Eisen
Fe
Iron
fer
ferrum
hierro
iron
iron atom
iron
IUPAC
26Fe
IUPAC
Eisen
ChEBI
Fe
IUPAC
Fe
UniProt
Iron
KEGG_COMPOUND
fer
ChEBI
ferrum
IUPAC
hierro
ChEBI
iron
ChEBI
Any nucleoside where the sugar component is D-ribose.
Ribonucleoside
a ribonucleoside
ribonucleosides
ribonucleoside
Ribonucleoside
KEGG_COMPOUND
a ribonucleoside
UniProt
ribonucleosides
ChEBI
An alpha-amino acid that is pentanoic acid bearing two amino substituents at positions 2 and 5.
2,5-diaminopentanoic acid
Ornithine
ornithine
2,5-Diaminopentanoic acid
2,5-Diaminovaleric acid
DL-Ornithine
Orn
ornithine
2,5-diaminopentanoic acid
IUPAC
Ornithine
KEGG_COMPOUND
ornithine
IUPAC
2,5-Diaminopentanoic acid
KEGG_COMPOUND
2,5-Diaminovaleric acid
KEGG_COMPOUND
DL-Ornithine
ChemIDplus
Orn
IUPAC
That part of DNA or RNA that may be involved in pairing.
Base
nucleobases
nucleobase
Base
KEGG_COMPOUND
nucleobases
ChEBI
manganese
25Mn
Mangan
Manganese
Mn
manganese
manganeso
manganum
manganese atom
manganese
IUPAC
25Mn
IUPAC
Mangan
NIST_Chemistry_WebBook
Manganese
KEGG_COMPOUND
Mn
IUPAC
Mn
UniProt
manganese
ChEBI
manganeso
ChEBI
manganum
ChEBI
An oxo monocarboxylic acid that is (3-oxocyclopentyl)acetic acid substituted by a (2Z)-pent-2-en-1-yl group at position 2 of the cyclopentane ring.
Jasmonic acid
{(1R,2R)-3-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl}acetic acid
(-)-Jasmonic acid
(-)-jasmonic acid
(1R,2R)-3-oxo-2-(2Z)-2-penten-ylcyclopentanacetic acid
(1R,2R)-3-oxo-2-(pent-2Z-enyl)-cyclopentaneacetic acid
2-{(1R,2R)-3-oxo-2-[(Z)-pent-2-enyl]cyclopentyl}acetate
Jasmonate
jasmonic acid
Jasmonic acid
KEGG_COMPOUND
{(1R,2R)-3-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl}acetic acid
IUPAC
(-)-Jasmonic acid
KEGG_COMPOUND
(-)-jasmonic acid
ChEBI
(1R,2R)-3-oxo-2-(2Z)-2-penten-ylcyclopentanacetic acid
ChEBI
(1R,2R)-3-oxo-2-(pent-2Z-enyl)-cyclopentaneacetic acid
LIPID_MAPS
2-{(1R,2R)-3-oxo-2-[(Z)-pent-2-enyl]cyclopentyl}acetate
IUBMB
Jasmonate
KEGG_COMPOUND
An acyclic branched or unbranched hydrocarbon having the general formula CnH2n+2, and therefore consisting entirely of hydrogen atoms and saturated carbon atoms.
Alkane
alkane
alkanes
Alkan
RH
alcane
alcanes
alcano
alcanos
an alkane
alkane
Alkane
KEGG_COMPOUND
alkane
IUPAC
alkanes
IUPAC
Alkan
ChEBI
RH
KEGG_COMPOUND
alcane
IUPAC
alcanes
IUPAC
alcano
IUPAC
alcanos
IUPAC
an alkane
UniProt
A phosphate ion that is the conjugate base of hydrogenphosphate.
phosphate
tetraoxidophosphate(3-)
tetraoxophosphate(3-)
tetraoxophosphate(V)
Orthophosphate
PHOSPHATE ION
PO4(3-)
Phosphate
[PO4](3-)
phosphate(3-)
phosphate
IUPAC
tetraoxidophosphate(3-)
IUPAC
tetraoxophosphate(3-)
IUPAC
tetraoxophosphate(V)
IUPAC
Orthophosphate
KEGG_COMPOUND
PHOSPHATE ION
PDBeChem
PO4(3-)
IUPAC
Phosphate
KEGG_COMPOUND
[PO4](3-)
IUPAC
A one-carbon compound consisting of a methine group triple bonded to a nitrogen atom
Hydrogen cyanide
hydridonitridocarbon
hydrogen cyanide
hydrogen(nitridocarbonate)
methanenitrile
Blausaeure
Cyanwasserstoff
HCN
[CHN]
formonitrile
hydrocyanic acid
hydrogen cyanide
Hydrogen cyanide
KEGG_COMPOUND
hydridonitridocarbon
IUPAC
hydrogen cyanide
IUPAC
hydrogen cyanide
UniProt
hydrogen(nitridocarbonate)
IUPAC
methanenitrile
IUPAC
Blausaeure
ChEBI
Cyanwasserstoff
NIST_Chemistry_WebBook
HCN
KEGG_COMPOUND
[CHN]
IUPAC
formonitrile
IUPAC
hydrocyanic acid
NIST_Chemistry_WebBook
hexane-2,5-diyl bis(methanesulfonate)
hex-3-yne-2,5-diyl bis(methanesulfonate)
D-mannitol 1,6-bis(methanesulfonate)
L-mannitol 1,6-bis(methanesulfonate)
Any polyunsaturated fatty acid carrying one or more hydroperoxy substituents.
hydroperoxy polyunsaturated fatty acids
hydroperoxy polyunsaturated fatty acid
hydroperoxy polyunsaturated fatty acids
ChEBI
4-amino-3-hydroxynaphthalene-1-sulfonic acid
1-amino-2-naphthol-4-sulfonic acid
1-amino-4-sulfo-2-naphthol
4-amino-3-hydroxynaphthalene-1-sulphonic acid
4-amino-3-hydroxynaphthalene-1-sulfonic acid
4-amino-3-hydroxynaphthalene-1-sulfonic acid
IUPAC
1-amino-2-naphthol-4-sulfonic acid
ChemIDplus
1-amino-4-sulfo-2-naphthol
ChemIDplus
4-amino-3-hydroxynaphthalene-1-sulphonic acid
ChemIDplus
A potassium salt that lacks C-H bonds
inorganic potassium salt
A haloalkane that is bromoethane substituted by chlorine at position 2.
1-bromo-2-chloroethane
1,2-bromochloroethane
1,2-chlorobromoethane
2-bromo-1-chloroethane
2-bromoethyl chloride
2-chloroethyl bromide
beta-chloroethyl bromide
ethylene chlorobromide
1-bromo-2-chloroethane
1-bromo-2-chloroethane
IUPAC
1,2-bromochloroethane
NIST_Chemistry_WebBook
1,2-chlorobromoethane
ChemIDplus
2-bromo-1-chloroethane
ChemIDplus
2-bromoethyl chloride
NIST_Chemistry_WebBook
2-chloroethyl bromide
NIST_Chemistry_WebBook
beta-chloroethyl bromide
NIST_Chemistry_WebBook
ethylene chlorobromide
ChemIDplus
are a type of flavonoid pigments in plants. Anthoxanthins are water-soluble pigments which range in color from white or colorless to a creamy to yellow, often on petals of flowers.
anthoxanthin
A chlorophenoxyacetate anion that is the conjugate base of (2,4-dichlorophenoxy)acetic acid, obtained by deprotonation of the carboxy group.
(2,4-dichlorophenoxy)acetate
2,4-D
2,4-dichlorophenoxyacetate
(2,4-dichlorophenoxy)acetate
(2,4-dichlorophenoxy)acetate
IUPAC
(2,4-dichlorophenoxy)acetate
UniProt
2,4-D
UM-BBD
2,4-dichlorophenoxyacetate
ChEBI
A member of the class of 1,4-benzoquinones that is p-benzoquinone in which the hydrogens at positions 2 and 5 are replaced by aziridin-1-yl groups.
2,5-bis(aziridin-1-yl)cyclohexa-2,5-diene-1,4-dione
2,5,-bis(ethyleneimine)-1,4-benzoquinone
2,5,-bisethylene-imine-1,4-benzoquinone
2,5-Bisaethyleniminobenzochinon-1,4
2,5-bis(1-aziridinyl)-2,5-cyclohexadiene-1,4-dione
2,5-bis(1-aziridinyl)-p-benzoquinone
2,5-bis(1-aziridynyl)benzoquinone
2,5-bis(aziridino)-1,4-benzoquinone
2,5-bis(aziridino)benzoquinone
2,5-bis(ethyleneimino)-1,4-benzoquinone
2,5-bis-ethyleniminobenzoquinone
2,5-bisethyleneiminebenzoquinone
2,5-di(ethyleneimino)-1,4-benzoquinone
2,5-diaziridinyl-1,4-benzoquinone
3,6-diaziridinyl-1,4-benzoquinone
DZQ
TW 13
ethylenimine quinone
2,5-bis(aziridin-1-yl)-1,4-benzoquinone
2,5-bis(aziridin-1-yl)cyclohexa-2,5-diene-1,4-dione
IUPAC
2,5,-bis(ethyleneimine)-1,4-benzoquinone
ChEBI
2,5,-bisethylene-imine-1,4-benzoquinone
ChEBI
2,5-Bisaethyleniminobenzochinon-1,4
ChEBI
2,5-bis(1-aziridinyl)-2,5-cyclohexadiene-1,4-dione
ChemIDplus
2,5-bis(1-aziridinyl)-p-benzoquinone
ChemIDplus
2,5-bis(1-aziridynyl)benzoquinone
ChemIDplus
2,5-bis(aziridino)-1,4-benzoquinone
ChemIDplus
2,5-bis(aziridino)benzoquinone
ChemIDplus
2,5-bis(ethyleneimino)-1,4-benzoquinone
ChemIDplus
2,5-bis-ethyleniminobenzoquinone
ChemIDplus
2,5-bisethyleneiminebenzoquinone
ChemIDplus
2,5-di(ethyleneimino)-1,4-benzoquinone
ChemIDplus
2,5-diaziridinyl-1,4-benzoquinone
ChemIDplus
3,6-diaziridinyl-1,4-benzoquinone
ChEBI
DZQ
ChEBI
TW 13
ChemIDplus
ethylenimine quinone
ChemIDplus
2,5-dibromo-3-methyl-6-(propan-2-yl)cyclohexa-2,5-diene-1,4-dione
2,5-dibromo-3-isopropyl-6-methyl-1,4-benzoquinone
2,5-dibromo-3-isopropyl-6-methylbenzoquinone
2,5-dibromo-3-methyl-6-(1-methylethyl)-2,5-cyclohexadiene-1,4-dione
2,5-dibromo-3-methyl-6-(1-methylethyl)cyclohexa-2,5-diene-1,4-dione
DBMIB
dibromothymoquinone
2,5-dibromo-3-methyl-6-(propan-2-yl)cyclohexa-2,5-diene-1,4-dione
IUPAC
2,5-dibromo-3-isopropyl-6-methyl-1,4-benzoquinone
IUPAC
2,5-dibromo-3-isopropyl-6-methylbenzoquinone
ChemIDplus
2,5-dibromo-3-methyl-6-(1-methylethyl)-2,5-cyclohexadiene-1,4-dione
ChemIDplus
2,5-dibromo-3-methyl-6-(1-methylethyl)cyclohexa-2,5-diene-1,4-dione
IUPAC
DBMIB
ChEBI
mitomycin C
mitomycin C(1-)
mitomycin C
UniProt
Any unsaturated fatty acid carrying one or more hydroperoxy substituents.
hydroperoxy unsaturated fatty acids
hydroperoxy unsaturated fatty acid
hydroperoxy unsaturated fatty acids
ChEBI
2-chloroethyl methanesulfonate
An N-acyl-D-alpha-amino acid anion resulting from deprotonation of both carboxy groups of N-acetyl-D-aspartic acid. Major microspecies at pH 7.3.
N-acetyl-D-Asp
N-acetyl-D-aspartate
N-acetyl-D-aspartate(2-)
N-acetyl-D-Asp
SUBMITTER
N-acetyl-D-aspartate
UniProt
2-fluoroethyl methanesulfonate
imidazolones
imidazolone
imidazolones
ChEBI
A pyrimidine having keto groups at the 2- and 4-positions and a bromo group at the 5-position. Used mainly as an experimental mutagen.
5-bromopyrimidine-2,4(1H,3H)-dione
1,2,3,4-tetrahydro-5-bromo-2,4-pyrimidinedione
5-BU
5-BrU
5-bromo-2,4(1H,3H)-pyrimidinedione
bromouracil
5-bromouracil
5-bromopyrimidine-2,4(1H,3H)-dione
IUPAC
1,2,3,4-tetrahydro-5-bromo-2,4-pyrimidinedione
NIST_Chemistry_WebBook
5-BU
ChemIDplus
5-BrU
ChemIDplus
5-bromo-2,4(1H,3H)-pyrimidinedione
NIST_Chemistry_WebBook
bromouracil
ChemIDplus
A uridine having a bromo substituent at the 5-position.
5-bromouridine
1-beta-ribofuranosyl-5-bromo-uracil
5-bromo-1-beta-D-ribofuranosylpyrimidine-2,4(1H,3H)-dione
BrU
5-bromouridine
5-bromouridine
ChEBI
5-bromouridine
IUPAC
5-bromouridine
UniProt
1-beta-ribofuranosyl-5-bromo-uracil
ChemIDplus
5-bromo-1-beta-D-ribofuranosylpyrimidine-2,4(1H,3H)-dione
ChEBI
BrU
ChEBI
An EC 2.5.1.* (non-methyl-alkyl or aryl transferase) inhibitor that interferes with the action of 3-phosphoshikimate 1-carboxyvinyltransferase (EC 2.5.1.19).
3-enol-pyruvoylshikimate-5-phosphate synthase inhibitor
3-enol-pyruvoylshikimate-5-phosphate synthase inhibitors
3-phosphoshikimate 1-carboxyvinyltransferase (EC 2.5.1.19) inhibitor
3-phosphoshikimate 1-carboxyvinyltransferase (EC 2.5.1.19) inhibitors
3-phosphoshikimate 1-carboxyvinyltransferase inhibitor
3-phosphoshikimate 1-carboxyvinyltransferase inhibitors
5-enolpyruvylshikimate-3-phosphate synthase inhibitor
5-enolpyruvylshikimate-3-phosphate synthase inhibitors
EC 2.5.1.19 (3-phosphoshikimate 1-carboxyvinyltransferase) inhibitors
EC 2.5.1.19 inhibitor
EC 2.5.1.19 inhibitors
EPSP synthase inhibitor
EPSP synthase inhibitors
phosphoenolpyruvate:3-phosphoshikimate 5-O-(1-carboxyvinyl)-transferase inhibitor
phosphoenolpyruvate:3-phosphoshikimate 5-O-(1-carboxyvinyl)-transferase inhibitors
EC 2.5.1.19 (3-phosphoshikimate 1-carboxyvinyltransferase) inhibitor
3-enol-pyruvoylshikimate-5-phosphate synthase inhibitor
ChEBI
3-enol-pyruvoylshikimate-5-phosphate synthase inhibitors
ChEBI
3-phosphoshikimate 1-carboxyvinyltransferase (EC 2.5.1.19) inhibitor
ChEBI
3-phosphoshikimate 1-carboxyvinyltransferase (EC 2.5.1.19) inhibitors
ChEBI
3-phosphoshikimate 1-carboxyvinyltransferase inhibitor
ChEBI
3-phosphoshikimate 1-carboxyvinyltransferase inhibitors
ChEBI
5-enolpyruvylshikimate-3-phosphate synthase inhibitor
ChEBI
5-enolpyruvylshikimate-3-phosphate synthase inhibitors
ChEBI
EC 2.5.1.19 (3-phosphoshikimate 1-carboxyvinyltransferase) inhibitors
ChEBI
EC 2.5.1.19 inhibitor
ChEBI
EC 2.5.1.19 inhibitors
ChEBI
EPSP synthase inhibitor
ChEBI
EPSP synthase inhibitors
ChEBI
phosphoenolpyruvate:3-phosphoshikimate 5-O-(1-carboxyvinyl)-transferase inhibitor
ChEBI
phosphoenolpyruvate:3-phosphoshikimate 5-O-(1-carboxyvinyl)-transferase inhibitors
ChEBI
Any aminopurine having the amino substituent at the 2-position.
2-aminopurines
2-aminopurines
2-aminopurines
ChEBI
Any compound having 6-aminopurine (adenine) as part of its structure.
6-aminopurines
6-aminopurines
6-aminopurines
ChEBI
A glycosyl compound arising formally from the elimination of water from a glycosidic hydroxy group and an H atom bound to a carbon atom, thus creating a C-C bond.
C-glycoside
C-glycosides
C-glycosyl compounds
C-glycosyl compound
C-glycoside
ChEBI
C-glycosides
ChEBI
C-glycosyl compounds
ChEBI
C19-gibberellins
C19-gibberellin
C19-gibberellins
ChEBI
N-(2-chloroethyl)-N'-(6-chloro-2-methoxyacridin-9-yl)-N-ethylpropane-1,3-diamine dihydrochloride
ICR 170
N-(2-chloroethyl)-N'-(6-chloro-2-methoxy-9-acridinyl)-N-ethyl-1,3-propanediamine dihydrochloride
acridine mustard
ICR-170
N-(2-chloroethyl)-N'-(6-chloro-2-methoxyacridin-9-yl)-N-ethylpropane-1,3-diamine dihydrochloride
IUPAC
ICR 170
ChemIDplus
N-(2-chloroethyl)-N'-(6-chloro-2-methoxy-9-acridinyl)-N-ethyl-1,3-propanediamine dihydrochloride
ChemIDplus
acridine mustard
ChemIDplus
3-(diethylamino)-7-{(E)-[4-(dimethylamino)phenyl]diazenyl}-5-phenylphenazin-5-ium chloride
3-(diethylamino)-7-((4-(dimethylamino)phenyl)azo)-5-phenylphenazinium chloride
3-(diethylamino)-7-((p-(dimethylamino)phenyl)azo)-5-phenylphenazinium chloride
Janus Green B
Janus Green V
Janus Green B chloride
3-(diethylamino)-7-{(E)-[4-(dimethylamino)phenyl]diazenyl}-5-phenylphenazin-5-ium chloride
IUPAC
3-(diethylamino)-7-((4-(dimethylamino)phenyl)azo)-5-phenylphenazinium chloride
ChemIDplus
3-(diethylamino)-7-((p-(dimethylamino)phenyl)azo)-5-phenylphenazinium chloride
ChemIDplus
Janus Green B
ChemIDplus
Janus Green V
ChemIDplus
An N-acetyl-amino acid having D-configuration.
N-Acetyl-D-amino-acid
N-acetyl-D-amino acids
N-acetyl-D-amino acid
N-Acetyl-D-amino-acid
KEGG_COMPOUND
N-acetyl-D-amino acids
ChEBI
An L-amino acid having an N-acetyl substituent.
N-acetyl-L-amino acid
An N-acyl-L-aspartic acid in which the acyl group is specified as acetyl.
(2S)-2-acetamidobutanedioic acid
(S)-2-(acetylamino)butanedioic acid
(S)-2-(acetylamino)succinic acid
L-N-acetylaspartic acid
N-acetylaspartic acid
NAA
acetyl-L-aspartic acid
acetylaspartic acid
N-acetyl-L-aspartic acid
(2S)-2-acetamidobutanedioic acid
IUPAC
(S)-2-(acetylamino)butanedioic acid
ChEBI
(S)-2-(acetylamino)succinic acid
HMDB
L-N-acetylaspartic acid
HMDB
N-acetylaspartic acid
ChemIDplus
NAA
HMDB
acetyl-L-aspartic acid
HMDB
acetylaspartic acid
ChemIDplus
An N-acyl-amino acid that has acetyl as the acyl group.
N-Acetyl amino acid
N-acetyl-amino acids
N-acetyl-amino acid
N-Acetyl amino acid
KEGG_COMPOUND
N-acetyl-amino acids
ChEBI
Any N-acylamino acid having L-configuration.
N-acyl-L-amino acid
L-Aspartic acid substituted at nitrogen by an acyl group.
N-acyl-L-aspartic acids
N-acyl-L-aspartic acid
N-acyl-L-aspartic acids
ChEBI
An aspartic acid derivative that is aspartic acid in which one of the hydrogens attached to the amino group is replaced by an acyl group.
N-acyl-aspartic acid
A glycosyl compound arising formally from the elimination of water from a glycosidic hydroxy group and an H atom bound to a nitrogen atom, thus creating a C-N bond.
glycosylamine
N-glycoside
N-glycosides
N-glycosyl compounds
glycosylamines
N-glycosyl compound
glycosylamine
IUPAC
N-glycoside
ChEBI
N-glycosides
ChEBI
N-glycosyl compounds
ChEBI
glycosylamines
IUPAC
An N-nitroguanidine compound having nitroso and methyl substituents at the N'-position
1-methyl-3-nitro-1-nitrosoguanidine
N-Methyl-N'-nitro-N-nitrosoguanidine
1-Methyl-1-nitroso-3-nitroguanidine
1-Methyl-3-nitro-1-nitrosoguanidine
1-Nitroso-3-nitro-1-methylguanidine
MNG
MNNG
Methylnitronitrosoguanidine
N'-Nitro-N-nitroso-N-methylguanidine
N-Methyl-N',2-dioxohydrazinecarboximidohydrazide 2-oxide
N-Methyl-N-nitroso-N'-nitroguanidine
N-Methyl-N-nitrosonitroguanidin
N-Nitroso-N-methyl-N'-nitroguanidine
N-methyl-N'-nitro-N-nitrosoguanidine
1-methyl-3-nitro-1-nitrosoguanidine
IUPAC
N-Methyl-N'-nitro-N-nitrosoguanidine
KEGG_COMPOUND
1-Methyl-1-nitroso-3-nitroguanidine
ChemIDplus
1-Methyl-3-nitro-1-nitrosoguanidine
KEGG_COMPOUND
1-Nitroso-3-nitro-1-methylguanidine
ChemIDplus
MNG
ChemIDplus
MNNG
ChemIDplus
MNNG
KEGG_COMPOUND
Methylnitronitrosoguanidine
KEGG_COMPOUND
N'-Nitro-N-nitroso-N-methylguanidine
ChemIDplus
N-Methyl-N',2-dioxohydrazinecarboximidohydrazide 2-oxide
NIST_Chemistry_WebBook
N-Methyl-N-nitroso-N'-nitroguanidine
ChEBI
N-Methyl-N-nitroso-N'-nitroguanidine
ChemIDplus
N-Methyl-N-nitrosonitroguanidin
ChEBI
N-Nitroso-N-methyl-N'-nitroguanidine
ChemIDplus
S-2-chloroethylcysteine
An organosulfur compound having the structure R2S=O or R2C=S=O (R =/= H).
sulfoxide
S-oxides
sulfoxides
sulfoxide
sulfoxide
ChEBI
S-oxides
ChEBI
sulfoxides
ChEBI
A member of the class of abscisic acids in which the double bond betweeen positions 2 and 3 has cis- (natural) geometry.
(2Z,4E)-5-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-3-methylpenta-2,4-dienoic acid
Abscisinsaeure
Abszisinsaeure
abscisic acid
acide abscissique
acido abscisico
2-cis-abscisic acid
(2Z,4E)-5-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-3-methylpenta-2,4-dienoic acid
IUPAC
Abscisinsaeure
ChEBI
Abszisinsaeure
ChEBI
abscisic acid
ChEBI
acide abscissique
ChEBI
acido abscisico
ChEBI
Compounds with the general formula RNHC(=O)CH3.
acetamides
Any amino acid derivative that is the N-acetyl or O-acetyl derivative of an amino acid.
acetyl-amino acids
acetyl-amino acid
acetyl-amino acids
ChEBI
acridines
An organic group formed by removing one or more hydroxy groups from an oxoacid that has the general structure RkE(=O)l(OH)m (l =/= 0). Although the term is almost always applied to organic compounds, with carboxylic acid as the oxoacid, acyl groups can in principle be derived from other types of acids such as sulfonic acids or phosphonic acids.
acyl group
alkanoyl
acyl groups
alkanoyl group
groupe acyle
acyl group
acyl group
IUPAC
alkanoyl
IUPAC
acyl groups
ChEBI
alkanoyl group
ChEBI
groupe acyle
IUPAC
alkaline earth metals
Erdalkalimetall
Erdalkalimetalle
alkaline earth metal
alkaline-earth metal
alkaline-earth metals
metal alcalino-terreux
metal alcalinoterreo
metales alcalinoterreos
metaux alcalino-terreux
alkaline earth metal atom
alkaline earth metals
IUPAC
Erdalkalimetall
ChEBI
Erdalkalimetalle
ChEBI
alkaline earth metal
ChEBI
alkaline-earth metal
ChEBI
alkaline-earth metals
ChEBI
metal alcalino-terreux
ChEBI
metal alcalinoterreo
ChEBI
metales alcalinoterreos
ChEBI
metaux alcalino-terreux
ChEBI
alkali metals
Alkalimetall
Alkalimetalle
alkali metal
metal alcalin
metal alcalino
metales alcalinos
metaux alcalins
alkali metal atom
alkali metals
IUPAC
Alkalimetall
ChEBI
Alkalimetalle
ChEBI
alkali metal
ChEBI
metal alcalin
ChEBI
metal alcalino
ChEBI
metales alcalinos
ChEBI
metaux alcalins
ChEBI
Any of the naturally occurring, basic nitrogen compounds (mostly heterocyclic) occurring mostly in the plant kingdom, but also found in bacteria, fungi, and animals. By extension, certain neutral compounds biogenetically related to basic alkaloids are also classed as alkaloids. Amino acids, peptides, proteins, nucleotides, nucleic acids, amino sugars and antibiotics are not normally regarded as alkaloids. Compounds in which the nitrogen is exocyclic (dopamine, mescaline, serotonin, etc.) are usually classed as amines rather than alkaloids.
Alkaloid
alkaloids
Alkaloide
alcaloide
alcaloides
alkaloid
Alkaloid
ChEBI
alkaloids
IUPAC
Alkaloide
ChEBI
alcaloide
ChEBI
alcaloides
ChEBI
A univalent group -CnH2n+1 derived from an alkane by removal of a hydrogen atom from any carbon atom.
alkyl group
alkyl groups
groupe alkyle
grupo alquilo
grupos alquilo
alkyl group
alkyl group
IUPAC
alkyl groups
IUPAC
groupe alkyle
IUPAC
grupo alquilo
IUPAC
grupos alquilo
IUPAC
aliphatic thioether
aliphatic thioethers
aliphatic sulfide
aliphatic thioether
ChEBI
aliphatic thioethers
ChEBI
Highly reactive chemical that introduces alkyl radicals into biologically active molecules and thereby prevents their proper functioning. It could be used as an antineoplastic agent, but it might be very toxic, with carcinogenic, mutagenic, teratogenic, and immunosuppressant actions. It could also be used as a component of poison gases.
alkylating agent
amino cyclitol glycoside
amino cyclitol glycosides
amino cyclitol glycoside
amino cyclitol glycoside
ChEBI
amino cyclitol glycosides
ChEBI
aminobenzoates
aminobenzoate
aminobenzoates
ChEBI
aminobenzoic acid
Aminobenzoesaeure
aminobenzoic acid
aminobenzoic acid
IUPAC
Aminobenzoesaeure
ChEBI
aminoglycoside antibiotics
aminoglycoside antibiotic
aminoglycoside antibiotics
ChEBI
4-aminofolic acid
N-(4-{[(2,4-diaminopteridin-6-yl)methyl]amino}benzoyl)-L-glutamic acid
4-amino-PGA
4-aminopteroylglutamic acid
N-(4-(((2,4-diamino-6-pteridinyl)methyl)amino)benzoyl)-L-glutamic acid
aminopterin
4-aminofolic acid
4-aminofolic acid
ChemIDplus
N-(4-{[(2,4-diaminopteridin-6-yl)methyl]amino}benzoyl)-L-glutamic acid
IUPAC
4-amino-PGA
ChemIDplus
4-aminopteroylglutamic acid
ChemIDplus
N-(4-(((2,4-diamino-6-pteridinyl)methyl)amino)benzoyl)-L-glutamic acid
ChemIDplus
aminopterin
ChemIDplus
Any purine having at least one amino substituent.
aminopurines
aminopurine
aminopurines
ChEBI
A monoatomic or polyatomic species having one or more elementary charges of the electron.
Anion
anion
Anionen
aniones
anions
anion
Anion
ChEBI
anion
ChEBI
anion
IUPAC
Anionen
ChEBI
aniones
ChEBI
anions
IUPAC
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
antioxidants
antioxydant
antoxidant
antioxidant
antioxidants
ChEBI
antioxydant
ChEBI
antoxidant
ChEBI
An L-alpha-amino acid which is L-aspartic acid or any of the essential amino acids biosynthesised from it (asparagine, lysine, methionine, threonine and isoleucine). A closed class.
aspartate family amino acids
aspartic acid family amino acid
aspartic acid family amino acids
oxaloacetate family amino acid
oxaloacetate family amino acids
oxaloacetate/aspartate family amino acid
oxaloacetate/aspartate family amino acids
aspartate family amino acid
aspartate family amino acids
ChEBI
aspartic acid family amino acid
ChEBI
aspartic acid family amino acids
ChEBI
oxaloacetate family amino acid
ChEBI
oxaloacetate family amino acids
ChEBI
oxaloacetate/aspartate family amino acid
ChEBI
oxaloacetate/aspartate family amino acids
ChEBI
An alpha-amino acid that consists of succinic acid bearing a single alpha-amino substituent
Aspartic acid
aspartic acid
(+-)-Aspartic acid
(R,S)-Aspartic acid
2-aminobutanedioic acid
Asp
D
DL-Aminosuccinic acid
DL-Asparagic acid
aspartic acid
Aspartic acid
KEGG_COMPOUND
aspartic acid
IUPAC
(+-)-Aspartic acid
ChemIDplus
(R,S)-Aspartic acid
ChemIDplus
2-aminobutanedioic acid
IUPAC
Asp
ChEBI
D
ChEBI
DL-Aminosuccinic acid
ChemIDplus
DL-Asparagic acid
ChemIDplus
An amino acid derivative resulting from reaction of aspartic acid at the amino group or either of the carboxy groups, or from the replacement of any hydrogen of aspartic acid by a heteroatom. The definition normally excludes peptides containing aspartic acid residues.
aspartic acid derivative
Any of a group of compounds, both naturally occurring and synthetic, that induce cell elongation in plant stems (from Greek alphaupsilonxialphanuomega, "to grow").
auxins
auxin
auxins
ChEBI
aziridines
A molecular entity having an available pair of electrons capable of forming a covalent bond with a hydron (Bronsted base) or with the vacant orbital of some other molecular entity (Lewis base).
Base
base
Base1
Base2
Basen
Nucleobase
bases
base
Base
ChEBI
base
ChEBI
base
IUPAC
Base1
KEGG_COMPOUND
Base2
KEGG_COMPOUND
Basen
ChEBI
Nucleobase
KEGG_COMPOUND
bases
ChEBI
Any benzenoid aromatic compound consisting of the benzene skeleton and its substituted derivatives.
benzenes
arenesulfonates
arenesulfonate oxoanion
arenesulfonates
ChEBI
A monocarboxylic acid anion obtained by deprotonation of the carboxy group of any benzoic acid.
benzoate anion
benzoates
benzoate anion
ChEBI
Any aromatic carboxylic acid that consists of benzene in which at least a single hydrogen has been substituted by a carboxy group.
benzoic acids
benzopyrans
benzopyran
benzopyrans
ChEBI
benzopyrroles
benzopyrrole
benzopyrroles
ChEBI
Any quinone resulting from the formal oxidation of catechol, hydroquinone, or their C-substituted derivatives.
benzoquinones
benzyl
Bn
C6H5-CH2-
phenylalanine side-chain
phenylmethyl
benzyl group
benzyl
IUPAC
Bn
ChEBI
C6H5-CH2-
IUPAC
phenylalanine side-chain
ChEBI
phenylmethyl
IUPAC
borate
trioxidoborate(3-)
(BO3)3-
BO3(3-)
[BO3](3-)
borate ion
trioxoborate(3-) ion
trioxoborate(III) anion
borate
borate
IUPAC
trioxidoborate(3-)
IUPAC
(BO3)3-
ChEBI
BO3(3-)
IUPAC
[BO3](3-)
IUPAC
borate ion
ChEBI
trioxoborate(3-) ion
ChEBI
trioxoborate(III) anion
ChEBI
Any inorganic anion that is formally derived from boric acid. The term includes polymeric anions containing chains of BO3 structural units sharing one oxygen atom (e.g. di-, tri-, and tetraborates) as well as chains or rings sharing two oxygen atoms (e.g. metaborates).
borate ion
borate anions
borate ions
borate ion
borate ion
ChEBI
borate anions
ChEBI
borate ions
ChEBI
boron molecular entity
boron compounds
boron molecular entities
boron molecular entity
boron molecular entity
ChEBI
boron compounds
ChEBI
boron molecular entities
ChEBI
brassinosteroids
brassinosteroid
brassinosteroids
ChEBI
A compound derived from a hydrocarbon by replacing a hydrogen atom with a bromine atom.
brominated hydrocarbons
bromohydrocarbons
bromohydrocarbon
brominated hydrocarbons
ChEBI
bromohydrocarbons
ChEBI
bromine
35Br
Br
Brom
brome
bromine
bromo
bromum
bromine atom
bromine
IUPAC
35Br
IUPAC
Br
ChEBI
Brom
ChEBI
brome
ChEBI
bromine
ChEBI
bromo
ChEBI
bromum
ChEBI
bromine molecular entity
bromine compounds
bromine molecular entities
bromine molecular entity
bromine molecular entity
ChEBI
bromine compounds
ChEBI
bromine molecular entities
ChEBI
Any haloalkane that consists of an alkane substituted by at least one bromine atom.
alkyl bromide
alkyl bromides
bromoalkanes
bromoalkane
alkyl bromide
ChEBI
alkyl bromides
ChEBI
bromoalkanes
ChEBI
A diol that is a butanediol or a derivative of a butanediol.
butanediols
cadmium
48Cd
Cd
Kadmium
cadmio
cadmium
cadmium atom
cadmium
IUPAC
48Cd
IUPAC
Cd
IUPAC
Kadmium
NIST_Chemistry_WebBook
cadmio
ChEBI
cadmium
ChEBI
cadmium compounds
cadmium molecular entities
cadmium molecular entity
cadmium compounds
ChEBI
cadmium molecular entities
ChEBI
calcium
20Ca
Ca
Calcium
Kalzium
calcio
calcium
calcium atom
calcium
IUPAC
20Ca
IUPAC
Ca
IUPAC
Ca
UniProt
Calcium
KEGG_COMPOUND
Kalzium
ChEBI
calcio
ChEBI
calcium
ChEBI
calcium molecular entity
calcium compounds
calcium molecular entities
calcium molecular entity
calcium molecular entity
ChEBI
calcium compounds
ChEBI
calcium molecular entities
ChEBI
Any ester of carbamic acid or its N-substituted derivatives.
carbamate esters
carbamates
carbamate ester
carbamate esters
ChEBI
carbamates
ChEBI
The univalent carboacyl group formed by loss of -OH from the carboxy group of carbamic acid.
carbamoyl
-C(O)NH2
-CONH2
aminocarbonyl
carbamyl
carbamyl group
carboxamide
carbamoyl group
carbamoyl
IUPAC
-C(O)NH2
ChEBI
-CONH2
IUPAC
aminocarbonyl
IUPAC
carbamyl
ChEBI
carbamyl group
ChEBI
carboxamide
IUPAC
Any carbohydrate derivative that exhibits antibiotic activity.
carbohydrate-containing antibiotic
carbon oxides
oxides of carbon
carbon oxide
carbon oxides
ChEBI
oxides of carbon
ChEBI
carbonyl
carbonyl group
>C=O
carbonyl group
carbonyl
IUPAC
carbonyl group
ChEBI
carbonyl group
UniProt
>C=O
IUPAC
Hydrocarbon carotenoids.
carotene
carotenes
carotenes
carotene
carotene
ChEBI
carotenes
IUPAC
carotenes
ChEBI
carotenoid epoxides
epoxycarotenoids
epoxycarotenoid
carotenoid epoxides
ChEBI
epoxycarotenoids
ChEBI
One of a class of tetraterpenoids (C40), formally derived from the acyclic parent, psi,psi-carotene by hydrogenation, dehydrogenation, cyclization, oxidation, or combination of these processes. This class includes carotenes, xanthophylls and certain compounds that arise from rearrangement of the skeleton of psi,psi-carotene or by loss of part of this structure. Retinoids are excluded.
carotenoid
carotenes and carotenoids
carotenoids
carotenoid
carotenoid
IUPAC
carotenes and carotenoids
ChemIDplus
carotenoids
ChEBI
carotenols
hydroxycarotenoids
carotenol
carotenols
ChEBI
hydroxycarotenoids
ChEBI
A substance intended to sterilize any organism.
chemosterilants
chemosterilant
chemosterilants
ChEBI
chloride salts
chlorides
chloride salt
chloride salts
ChEBI
chlorides
ChEBI
chlorine
17Cl
Chlor
Cl
chlore
chlorine
chlorum
cloro
chlorine atom
chlorine
IUPAC
17Cl
IUPAC
Chlor
ChEBI
Cl
IUPAC
chlore
ChEBI
chlorine
ChEBI
chlorum
ChEBI
cloro
ChEBI
A halogen molecular entity containing one or more atoms of chlorine.
chlorine molecular entity
Any haloalkane that consists of an alkane substituted by at least one chloro group.
chloroalkane
alkyl chloride
alkyl chlorides
chloroalkanes
chloroalkane
chloroalkane
ChEBI
alkyl chloride
ChEBI
alkyl chlorides
ChEBI
chloroalkanes
ChEBI
Any organochlorine compound containing a benzene ring which is substituted by one or more chlorines.
chlorobenzenes
A monocarboxylic acid anion obtained by deprotonation of the carboxy group of any chlorophenoxyacetic acid.
chlorophenoxyacetate anion
A monocarboxylic acid that is phenoxyacetic acid in which at least one of the phenyl hydrogens is replaced by chlorine.
chlorophenoxyacetic acids
chlorophenoxyacetic acid
chlorophenoxyacetic acids
ChEBI
chromenes
chromopeptide
Any alpha,beta-unsaturated monocarboxylic acid based on the cinnamic acid skeleton and its substituted derivatives.
cinnamic acids
An organic molecule or ion (usually a metal ion) that is required by an enzyme for its activity. It may be attached either loosely (coenzyme) or tightly (prosthetic group).
cofactor
cofactors
cofactor
cofactor
IUPAC
cofactors
IUPAC
An alkaloid that is a carbotricyclic compound comprising 5,6,7,9-tetrahydrobenzo[a]heptalene having four methoxy substituents at the 1-, 2-, 3- and 10-positions as well as an oxo group at the 9-position and an acetamido group at the 7-position. It has been isolated from the plants belonging to genus Colchicum.
N-(1,2,3,10-tetramethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-7-yl)acetamide
colchicine
N-(1,2,3,10-tetramethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-7-yl)acetamide
IUPAC
compatible osmolytes
Any constitutionally or isotopically distinct atom, molecule, ion, ion pair, radical, radical ion, complex, conformer etc., identifiable as a separately distinguishable entity.
molecular entity
entidad molecular
entidades moleculares
entite moleculaire
molecular entities
molekulare Entitaet
molecular entity
molecular entity
IUPAC
entidad molecular
IUPAC
entidades moleculares
IUPAC
entite moleculaire
IUPAC
molecular entities
IUPAC
molekulare Entitaet
ChEBI
copper molecular entity
copper compounds
copper molecular entities
copper molecular entity
copper molecular entity
ChEBI
copper compounds
ChEBI
copper molecular entities
ChEBI
copper cation
Cu cation
copper cations
copper cation
copper cation
IUPAC
Cu cation
UniProt
copper cations
ChEBI
A metal sulfate compound having copper(2+) as the metal ion.
Copper(II) sulfate
copper(2+) sulfate
copper(II) sulfate
CuSO4
Cupric sulfate
copper sulfate
cupric sulfate anhydrous
copper(II) sulfate
Copper(II) sulfate
KEGG_COMPOUND
copper(2+) sulfate
IUPAC
copper(II) sulfate
IUPAC
CuSO4
IUPAC
Cupric sulfate
ChemIDplus
copper sulfate
ChemIDplus
cupric sulfate anhydrous
ChemIDplus
A polyol consisting of a cycloalkane containing at least three hydroxy groups, each attached to a different ring carbon atom.
cyclitols
cyclitol
cyclitols
IUPAC
An amino acid derivative resulting from reaction of cysteine at the amino group, carboxy group, or thiol group, or from the replacement of any hydrogen of cysteine by a heteroatom. The definition normally excludes peptides containing cysteine residues.
cysteine derivative
cysteine derivatives
cysteine derivative
cysteine derivative
ChEBI
cysteine derivatives
ChEBI
cytochrome-b6f complex inhibitor
A phytohormone that promote cell division, or cytokinesis, in plant roots and shoots.
cytokinin
A herbicide which when sprayed or dusted on plants causes its leaves to fall off.
Defoliationsmittel
Entlaubungsmittel
defoliants
defoliant
Defoliationsmittel
ChEBI
Entlaubungsmittel
ChEBI
defoliants
ChEBI
An azole that is either one of a pair of heterocyclic organic compounds comprising three carbon atoms and two nitrogen atoms arranged in a ring.
diazoles
diazole
diazoles
ChEBI
Any member of the class of chlorobenzenes carrying two chloro groups at unspecified positions.
dichlorobenzene
Dichlorbenzol
dichlorobenzenes
dichlorobenzene
dichlorobenzene
ChEBI
dichlorobenzene
IUPAC
Dichlorbenzol
ChEBI
dichlorobenzenes
ChEBI
2,2'-bioxirane
1,1'-bi[ethylene oxide]
1,2:3,4-butadiene diepoxide
1,2:3,4-dianhydrothreitol
1,2:3,4-diepoxybutane
1,3-butadiene diepoxide
Butadiendioxyd
DEB
bioxirane
butadiene diepoxide
butadiene dioxide
butane diepoxide
dioxybutadiene
diepoxybutane
2,2'-bioxirane
IUPAC
1,1'-bi[ethylene oxide]
NIST_Chemistry_WebBook
1,2:3,4-butadiene diepoxide
ChemIDplus
1,2:3,4-dianhydrothreitol
NIST_Chemistry_WebBook
1,2:3,4-diepoxybutane
ChemIDplus
1,3-butadiene diepoxide
NIST_Chemistry_WebBook
Butadiendioxyd
ChemIDplus
DEB
NIST_Chemistry_WebBook
bioxirane
NIST_Chemistry_WebBook
butadiene diepoxide
NIST_Chemistry_WebBook
butadiene dioxide
NIST_Chemistry_WebBook
butane diepoxide
NIST_Chemistry_WebBook
dioxybutadiene
ChemIDplus
A compound that contains two hydroxy groups, generally assumed to be, but not necessarily, alcoholic. Aliphatic diols are also called glycols.
diols
diol
diols
IUPAC
Any terpenoid derived from a diterpene. The term includes compounds in which the C20 skeleton of the parent diterpene has been rearranged or modified by the removal of one or more skeletal atoms (generally methyl groups).
diterpenoids
C20 isoprenoids
diterpenoides
diterpenoid
diterpenoids
IUPAC
C20 isoprenoids
LIPID_MAPS
diterpenoides
ChEBI
Any substance which when absorbed into a living organism may modify one or more of its functions. The term is generally accepted for a substance taken for a therapeutic purpose, but is also commonly used for abused substances.
drugs
medicine
drug
drugs
ChEBI
medicine
ChEBI
monoatomic anions
monoatomic anion
monoatomic anions
ChEBI
monoatomic cations
monoatomic cation
monoatomic cations
ChEBI
A compound or agent that combines with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction.
enzyme inhibitor
enzyme inhibitors
inhibidor enzimatico
inhibidores enzimaticos
inhibiteur enzymatique
inhibiteurs enzymatiques
enzyme inhibitor
enzyme inhibitor
IUPAC
enzyme inhibitors
ChEBI
inhibidor enzimatico
ChEBI
inhibidores enzimaticos
ChEBI
inhibiteur enzymatique
ChEBI
inhibiteurs enzymatiques
ChEBI
A methanesulfonate ester resulting from the formal condensation of methanesulfonic acid with ethanol.
EMS
ethyl mesylate
ethyl methanesulphonate
methylsulfonic acid ethyl ester
methylsulfonic acid, ethyl ester
ethyl methanesulfonate
EMS
ChemIDplus
ethyl mesylate
ChemIDplus
ethyl methanesulphonate
ChemIDplus
methylsulfonic acid ethyl ester
ChemIDplus
methylsulfonic acid, ethyl ester
ChemIDplus
A member of the class of N-nitrosoureas that is urea in which one of the nitrogens is substituted by ethyl and nitroso groups.
1-ethyl-1-nitrosourea
1-(Aminocarbonyl)-1-ethyl-2-oxohydrazine
1-Ethyl-1-nitrosourea
Aethylnitroso-harnstoff
ENU
Ethyl nitrosourea
N-Ethyl-N-nitroso carbamide
N-Ethyl-N-nitroso-urea
N-Ethylnitrosourea
NEU
N-ethyl-N-nitrosourea
1-ethyl-1-nitrosourea
IUPAC
1-(Aminocarbonyl)-1-ethyl-2-oxohydrazine
NIST_Chemistry_WebBook
1-Ethyl-1-nitrosourea
ChemIDplus
Aethylnitroso-harnstoff
ChemIDplus
ENU
ChemIDplus
Ethyl nitrosourea
ChemIDplus
N-Ethyl-N-nitroso carbamide
ChemIDplus
N-Ethyl-N-nitroso-urea
ChemIDplus
N-Ethylnitrosourea
ChemIDplus
NEU
NIST_Chemistry_WebBook
An aliphatic sulfide in which the sulfur atom is bonded to at least one ethyl group.
ethyl sulfides
ethyl sulfide
ethyl sulfides
ChEBI
ferulic acids
A member of the class of flavonoid with a 2-aryl-1-benzopyran-4-one (2-arylchromen-4-one) skeleton and its substituted derivatives.
2-aryl-1-benzopyran-4-one
2-aryl-1-benzopyran-4-ones
2-arylchromen-4-one
2-arylchromen-4-ones
a flavone
flavones
2-aryl-1-benzopyran-4-one
ChEBI
2-aryl-1-benzopyran-4-ones
ChEBI
2-arylchromen-4-one
ChEBI
2-arylchromen-4-ones
ChEBI
a flavone
UniProt
fluoride salts
fluorides
fluoride salt
fluoride salts
ChEBI
fluorides
ChEBI
fluorine
9F
F
Fluor
fluor
fluorine
fluorum
fluorine atom
fluorine
IUPAC
9F
IUPAC
F
IUPAC
Fluor
ChemIDplus
fluor
ChEBI
fluorine
ChEBI
fluorum
ChEBI
fluorine molecular entity
fluorine compounds
fluorine molecular entities
fluorine molecular entity
fluorine molecular entity
ChEBI
fluorine compounds
ChEBI
fluorine molecular entities
ChEBI
A substance used to destroy fungal pests.
fungicides
fungicide
fungicides
ChEBI
Compounds containing at least one furan ring.
oxacyclopenta-2,4-dienes
furans
oxacyclopenta-2,4-dienes
ChEBI
gibberellins
gibberellin
gibberellins
ChEBI
Any hexosamine that is glucose in which at least one of the hydroxy groups has been replaced by an amino group.
glucosamines
An amino acid derivative resulting from reaction of glutamic acid at the amino group or either of the carboxy groups, or from the replacement of any hydrogen by a heteroatom. The definition normally excludes peptides containing glutamic acid residues.
glutamic acid derivative
An L-alpha-amino acid which is L-glutamic acid or any of the essential amino acids biosynthesised from it (glutamine, proline and arginine). A closed class.
glutamine family amino acids
glutamine family amino acid
glutamine family amino acids
ChEBI
An EC 6.3.* (C-N bond-forming ligase) inhibitor that interferes with the action of glutamate--ammonia ligase (EC 6.3.1.2).
EC 6.3.1.2 (glutamate--ammonia ligase) inhibitors
EC 6.3.1.2 inhibitor
EC 6.3.1.2 inhibitors
L-glutamate:ammonia ligase (ADP-forming) inhibitor
L-glutamate:ammonia ligase (ADP-forming) inhibitors
L-glutamine synthetase inhibitor
L-glutamine synthetase inhibitors
glutamate--ammonia ligase (EC 6.3.1.2) inhibitor
glutamate--ammonia ligase (EC 6.3.1.2) inhibitors
glutamate--ammonia ligase inhibitor
glutamate--ammonia ligase inhibitors
glutamine synthetase inhibitor
glutamine synthetase inhibitors
glutamylhydroxamic synthetase inhibitor
glutamylhydroxamic synthetase inhibitors
EC 6.3.1.2 (glutamate--ammonia ligase) inhibitor
EC 6.3.1.2 (glutamate--ammonia ligase) inhibitors
ChEBI
EC 6.3.1.2 inhibitor
ChEBI
EC 6.3.1.2 inhibitors
ChEBI
L-glutamate:ammonia ligase (ADP-forming) inhibitor
ChEBI
L-glutamate:ammonia ligase (ADP-forming) inhibitors
ChEBI
L-glutamine synthetase inhibitor
ChEBI
L-glutamine synthetase inhibitors
ChEBI
glutamate--ammonia ligase (EC 6.3.1.2) inhibitor
ChEBI
glutamate--ammonia ligase (EC 6.3.1.2) inhibitors
ChEBI
glutamate--ammonia ligase inhibitor
ChEBI
glutamate--ammonia ligase inhibitors
ChEBI
glutamine synthetase inhibitor
ChEBI
glutamine synthetase inhibitors
ChEBI
glutamylhydroxamic synthetase inhibitor
ChEBI
glutamylhydroxamic synthetase inhibitors
ChEBI
A proteinogenic amino acid derivative resulting from reaction of glycine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
glycine derivative
A glycosyl compound resulting from the attachment of a glycosyl group to a non-acyl group RO-, RS-, RSe-, etc. The bond between the glycosyl group and the non-acyl group is called a glycosidic bond. By extension, the terms N-glycosides and C-glycosides are used as class names for glycosylamines and for compounds having a glycosyl group attached to a hydrocarbyl group respectively. These terms are misnomers and should not be used. The preferred terms are glycosylamines and C-glycosyl compounds, respectively.
glycosides
O-glycoside
O-glycosides
glycosides
glycoside
glycosides
IUPAC
O-glycoside
ChEBI
O-glycosides
ChEBI
glycosides
ChEBI
Any disaccharide in which the two monosaccharide components are connected by a glycosidic linkage between their anomeric centres.
glycosyl glycoside
glycosyl glycosides
glycosyl glycoside
glycosyl glycoside
ChEBI
glycosyl glycosides
ChEBI
A chemical entity is a physical entity of interest in chemistry including molecular entities, parts thereof, and chemical substances.
chemical entity
chemical entity
chemical entity
UniProt
A role played by the molecular entity or part thereof within a biological context.
biological function
biological role
biological function
ChEBI
A defined linked collection of atoms or a single atom within a molecular entity.
group
Gruppe
Rest
groupe
grupo
grupos
group
group
IUPAC
Gruppe
ChEBI
Rest
ChEBI
groupe
IUPAC
grupo
IUPAC
grupos
IUPAC
Any organonitrogen compound containing a carbamimidamido (guanidino) group. Guanidines have the general structure (R(1)R(2)N)(R(3)R(4)N)C=N-R(5) and are related structurally to amidines and ureas.
guanidines
A halohydrocarbon that is an alkane in which at least one hydrogen atom has been replaced by with a halogen atom.
alkyl halide
alkyl halides
haloalkanes
haloalkane
alkyl halide
ChEBI
alkyl halides
ChEBI
haloalkanes
ChEBI
halogen molecular entity
halogen compounds
halogen molecular entities
halogen molecular entity
halogen molecular entity
ChEBI
halogen compounds
ChEBI
halogen molecular entities
ChEBI
A compound derived from a hydrocarbon by replacing a hydrogen atom with a halogen atom.
halogenated hydrocarbons
halohydrocarbons
halohydrocarbon
halogenated hydrocarbons
ChEBI
halohydrocarbons
ChEBI
halogen
halogens
Halogene
group 17 elements
group VII elements
halogene
halogenes
halogeno
halogenos
halogen
halogen
IUPAC
halogens
IUPAC
Halogene
ChEBI
group 17 elements
ChEBI
group VII elements
ChEBI
halogene
ChEBI
halogenes
ChEBI
halogeno
ChEBI
halogenos
ChEBI
A substance used to destroy plant pests.
Herbizid
Unkrautbekaempfungsmittel
Unkrautvertilgungsmittel
Wildkrautbekaempfungsmittel
herbicides
herbicide
Herbizid
ChEBI
Unkrautbekaempfungsmittel
ChEBI
Unkrautvertilgungsmittel
ChEBI
Wildkrautbekaempfungsmittel
ChEBI
herbicides
ChEBI
A cyclic compound having as ring members atoms of carbon and at least of one other element.
organic heterocycle
organic heterocyclic compounds
organic heterocyclic compound
organic heterocycle
ChEBI
organic heterocyclic compounds
ChEBI
N,N,N',N',N'',N''-hexamethyl-1,3,5-triazine-2,4,6-triamine
2,4,6-tris(dimethylamino)-1,3,5-triazine
2,4,6-tris(dimethylamino)-s-triazine
HMM
Hexalen
Hexastat
altretamina
altretamine
altretaminum
hexamethylmelamine
N,N,N',N',N'',N''-hexamethyl-1,3,5-triazine-2,4,6-triamine
IUPAC
2,4,6-tris(dimethylamino)-1,3,5-triazine
ChemIDplus
2,4,6-tris(dimethylamino)-s-triazine
NIST_Chemistry_WebBook
HMM
ChemIDplus
Hexalen
ChemIDplus
Hexastat
ChemIDplus
altretamina
ChemIDplus
altretamine
ChemIDplus
altretaminum
ChemIDplus
N,N,N',N',N'',N''-hexamethylphosphoric triamide
hexamethylphosphoric triamide
HEMPA
HMPA
HMPT
HMPTA
Hexamethylphosphoramid
Hexamethylphosphorsaeuretriamid
hexamethylorthophosphoric triamide
hexamethylphosphoramide
hexamethylphosphoric acid triamide
phosphoric acid hexamethyltriamide
phosphoric hexamethyltriamide
phosphoric tris(dimethylamide)
hexamethylphosphoric triamide
N,N,N',N',N'',N''-hexamethylphosphoric triamide
IUPAC
hexamethylphosphoric triamide
ChemIDplus
HEMPA
NIST_Chemistry_WebBook
HMPA
ChemIDplus
HMPA
KEGG_COMPOUND
HMPT
ChemIDplus
HMPTA
ChemIDplus
Hexamethylphosphoramid
ChEBI
Hexamethylphosphorsaeuretriamid
ChEBI
hexamethylorthophosphoric triamide
NIST_Chemistry_WebBook
hexamethylphosphoramide
ChEBI
hexamethylphosphoric acid triamide
ChemIDplus
phosphoric acid hexamethyltriamide
NIST_Chemistry_WebBook
phosphoric hexamethyltriamide
NIST_Chemistry_WebBook
phosphoric tris(dimethylamide)
NIST_Chemistry_WebBook
hexitol
hexitols
hexitol
hexitol
ChEBI
hexitols
ChEBI
Any 6-carbon amino monosaccharide with at least one alcoholic hydroxy group replaced by an amino group.
hexosamine
hexosamines
hexosamine
hexosamine
ChEBI
hexosamines
ChEBI
Originally referring to an endogenous compound that is formed in specialized organ or group of cells and carried to another organ or group of cells, in the same organism, upon which it has a specific regulatory function, the term is now commonly used to include non-endogenous, semi-synthetic and fully synthetic analogues of such compounds.
endocrine
hormones
hormone
endocrine
ChEBI
hormones
ChEBI
A compound consisting of carbon and hydrogen only.
hydrocarbon
hydrocarbons
Kohlenwasserstoff
Kohlenwasserstoffe
hidrocarburo
hidrocarburos
hydrocarbure
hydrocarbon
hydrocarbon
IUPAC
hydrocarbons
IUPAC
Kohlenwasserstoff
ChEBI
Kohlenwasserstoffe
ChEBI
hidrocarburo
IUPAC
hidrocarburos
IUPAC
hydrocarbure
IUPAC
Benzenediols that have the hydroxy substituents in the 1- and 4-positions.
1,4-benzoquinols
a 1,4-benzoquinol
a quinol
benzene-1,4-diols
hydroquinones
1,4-benzoquinols
ChEBI
a 1,4-benzoquinol
ChEBI
a quinol
UniProt
benzene-1,4-diols
ChEBI
Hydroxides are chemical compounds containing a hydroxy group or salts containing hydroxide (OH(-)).
hydroxides
Any carboxylic acid with at least one hydroxy group.
hydroxy carboxylic acids
hydroxycarboxylic acid
hydroxycarboxylic acids
hydroxy carboxylic acid
hydroxy carboxylic acids
ChEBI
hydroxycarboxylic acid
ChEBI
hydroxycarboxylic acids
ChEBI
Any benzoate derivative carrying a single carboxylate group and at least one hydroxy substituent.
hydroxybenzoates
hydroxybenzoate
hydroxybenzoates
ChEBI
Any benzoic acid carrying one or more phenolic hydroxy groups on the benzene ring.
hydroxybenzoic acid
hydroxybenzoic acids
hydroxybenzoic acid
hydroxybenzoic acid
IUPAC
hydroxybenzoic acids
ChEBI
An alpha-hydroxy ketone in which the carbonyl group and the hydroxy group are linked by a carbon bearing one hydrogen and one organyl group. Secondary alpha-hydroxy ketones are also known as acyloins, and are formally derived from reductive coupling of two carboxylic acid groups.
acyloin
acyloins
secondary alpha-hydroxy ketones
secondary alpha-hydroxy-ketone
secondary alpha-hydroxy-ketones
secondary alpha-hydroxyketone
secondary alpha-hydroxyketones
secondary alpha-hydroxy ketone
acyloin
ChEBI
acyloins
ChEBI
secondary alpha-hydroxy ketones
ChEBI
secondary alpha-hydroxy-ketone
ChEBI
secondary alpha-hydroxy-ketones
ChEBI
secondary alpha-hydroxyketone
ChEBI
secondary alpha-hydroxyketones
ChEBI
monohydroxycinnamic acids
monohydroxycinnamic acid
monohydroxycinnamic acids
ChEBI
Any member of the class of cinnamic acids carrying one or more hydroxy substituents.
hydroxycinnamic acids
hydroxycinnamic acid
hydroxycinnamic acids
ChEBI
Any flavone in which one or more ring hydrogens are replaced by hydroxy groups.
hydroxyflavones
hydroxyflavone
hydroxyflavones
ChEBI
Any member of the class of naphthalenes that is naphthalene carrying one or more hydroxy groups.
hydroxynaphthalene
hygromycins
hygromycin
hygromycins
ChEBI
A five-membered organic heterocycle containing two nitrogen atoms at positions 1 and 3, or any of its derivatives; compounds containing an imidazole skeleton.
imidazoles
imidazolinones
imidazolinone
imidazolinones
ChEBI
An indol-3-yl carboxylic acid in which the carboxylic acid specified is acetic acid.
indole-3-acetic acids
Any indolyl carboxylic acid carrying an indol-3-yl or substituted indol-3-yl group.
indol-3-yl carboxylic acids
indol-3-yl carboxylic acid
indol-3-yl carboxylic acids
ChEBI
Any compound containing an indole skeleton.
indoles
A compound which contains oxygen, at least one other element, and at least one hydrogen bound to oxygen, and which produces a conjugate base by loss of positive hydrogen ion(s) (hydrons).
oxoacid
oxoacids
oxacids
oxiacids
oxo acid
oxy-acids
oxyacids
oxoacid
oxoacid
IUPAC
oxoacids
IUPAC
oxacids
ChEBI
oxiacids
ChEBI
oxo acid
ChEBI
oxy-acids
ChEBI
oxyacids
ChEBI
inorganic anions
inorganic anion
inorganic anions
ChEBI
A molecular entity that contains no carbon.
anorganische Verbindungen
inorganic compounds
inorganic entity
inorganic molecular entities
inorganics
inorganic molecular entity
anorganische Verbindungen
ChEBI
inorganic compounds
ChEBI
inorganic entity
ChEBI
inorganic molecular entities
ChEBI
inorganics
ChEBI
inorganic oxides
inorganic oxide
inorganic oxides
ChEBI
Compounds of structure ROOR' in which R and R' are inorganic groups.
inorganic peroxide
inorganic peroxides
inorganic peroxide
inorganic peroxide
ChEBI
inorganic peroxides
ChEBI
anorganisches Salz
inorganic salts
inorganic salt
anorganisches Salz
ChEBI
inorganic salts
ChEBI
inorganic sulfate salts
inorganic sulfates
inorganic sulfate salt
inorganic sulfate salts
ChEBI
inorganic sulfates
ChEBI
Strictly, a substance intended to kill members of the class Insecta. In common usage, any substance used for preventing, destroying, repelling or controlling insects.
insecticides
insecticide
insecticides
ChEBI
A role played by a chemical agent which exhibits the capability of occupying space between DNA base pairs due to particular properties in size, shape and charge. Intercalation of chemical compounds in DNA helix can result in replication errors (shift, mutation) or DNA damages.
agente intercalante
intercalating agent
intercalating agents
intercalating ligands
intercalators
intercalator
agente intercalante
ChEBI
intercalating agent
ChEBI
intercalating agents
ChEBI
intercalating ligands
ChEBI
intercalators
ChEBI
Chemical element with atomic number 53.
iodine
53I
I
Iod
J
Jod
iode
iodine
iodium
yodo
iodine atom
iodine
IUPAC
53I
IUPAC
I
ChEBI
Iod
ChEBI
J
ChEBI
Jod
ChEBI
iode
ChEBI
iodine
ChEBI
iodium
ChEBI
yodo
ChEBI
A salt is an assembly of cations and anions.
salt
Salz
Salze
ionic compound
ionic compounds
sal
sales
salts
sel
sels
salt
salt
IUPAC
Salz
ChEBI
Salze
ChEBI
ionic compound
ChEBI
ionic compounds
ChEBI
sal
ChEBI
sales
ChEBI
salts
ChEBI
sel
ChEBI
sels
ChEBI
monoatomic ions
monoatomic ion
monoatomic ions
ChEBI
organic salts
organisches Salz
organic salt
organic salts
ChEBI
organisches Salz
ChEBI
A molecular entity having a net electric charge.
Ion
ion
Ionen
iones
ions
ion
Ion
ChEBI
ion
ChEBI
ion
IUPAC
Ionen
ChEBI
iones
ChEBI
ions
ChEBI
iron molecular entity
iron compounds
iron molecular entities
iron molecular entity
iron molecular entity
ChEBI
iron compounds
ChEBI
iron molecular entities
ChEBI
iron cation
Fe cation
iron cations
iron cation
iron cation
IUPAC
Fe cation
UniProt
iron cations
ChEBI
Any lipid formally derived from isoprene (2-methylbuta-1,3-diene), the skeleton of which can generally be discerned in repeated occurrence in the molecule. The skeleton of isoprenoids may differ from strict additivity of isoprene units by loss or shift of a fragment, commonly a methyl group. The class includes both hydrocarbons and oxygenated derivatives.
isoprenoid
isoprenoids
isoprenoids
isoprenoid
isoprenoid
ChEBI
isoprenoids
IUPAC
isoprenoids
ChEBI
Any alkaloid that has a structure based on an isoquinoline nucleus. They are derived from the amino acids like tyrosine and phenylalanine.
isoquinoline alkaloids
isoquinoline alkaloid
isoquinoline alkaloids
ChEBI
The jasmonates (JAs) are a group of plant hormones which help regulate plant growth and development.
jasmonates
Any hexose containing a single ketone group.
ketohexose
ketohexoses
ketohexose
ketohexose
ChEBI
ketohexoses
ChEBI
Ketonic parent sugars (polyhydroxy ketones H[CH(OH)]nC(=O)[CH(OH)]mH) and their intramolecular hemiketals.
ketose
ketoses
ketose
ketose
ChEBI
ketoses
ChEBI
Any cyclic carboxylic ester containing a 1-oxacycloalkan-2-one structure, or an analogue having unsaturation or heteroatoms replacing one or more carbon atoms of the ring.
lactone
lactones
Lacton
Lakton
Laktone
lactona
lactonas
lactone
lactone
IUPAC
lactones
IUPAC
Lacton
ChEBI
Lakton
ChEBI
Laktone
ChEBI
lactona
IUPAC
lactonas
IUPAC
A two-membered subclass of octadecatrienoic acid comprising the (9Z,12Z,15Z)- and (6Z,9Z,12Z)-isomers. Linolenic acids are nutrients essential to the formation of prostaglandins and are also used in making paints and synthetic resins.
C18:3
Linolensaeure
linolenic acids
linolenic acid
C18:3
ChEBI
Linolensaeure
ChEBI
linolenic acids
ChEBI
magnesium
12Mg
Magnesium
Mg
magnesio
magnesium
magnesium atom
magnesium
IUPAC
12Mg
IUPAC
Magnesium
ChEBI
Mg
IUPAC
Mg
UniProt
magnesio
ChEBI
magnesium
ChEBI
magnesium molecular entity
magnesium compounds
magnesium molecular entities
magnesium molecular entity
magnesium molecular entity
ChEBI
magnesium compounds
ChEBI
magnesium molecular entities
ChEBI
magnesium porphyrins
magnesium porphyrin
magnesium porphyrins
ChEBI
manganese molecular entity
manganese compounds
manganese molecular entities
manganese molecular entity
manganese molecular entity
ChEBI
manganese compounds
ChEBI
manganese molecular entities
ChEBI
manganese cation
manganese cations
manganese cation
manganese cation
IUPAC
manganese cations
ChEBI
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
metabolite
metabolites
primary metabolites
secondary metabolites
metabolite
metabolite
IUPAC
metabolites
ChEBI
primary metabolites
ChEBI
secondary metabolites
ChEBI
a metal cation
metal cations
metal cation
a metal cation
UniProt
metal cations
ChEBI
metalloporphyrins
metaloporphyrins
metalloporphyrin
metalloporphyrins
ChEBI
metaloporphyrins
ChEBI
An organosulfonic ester resulting from the formal condensation of methanesulfonic acid with the hydroxy group of an alcohol, phenol, heteroarenol, or enol.
mesylate ester
mesylate esters
methanesulfonic acid esters
methanesulfonate ester
mesylate ester
ChEBI
mesylate esters
ChEBI
methanesulfonic acid esters
ChEBI
A 1,1-diunsubstituted alkanesulfonate that is the conjugate base of methanesulfonic acid.
methanesulfonate
methylsulfonate
methanesulfonate
methanesulfonate
IUPAC
methanesulfonate
UniProt
methylsulfonate
UM-BBD
N-ethyl-1-methoxy-N-nitrosoethanamine
1-methoxy-N-nitrosodiethylamine
N-ethyl-1-methoxy-N-nitrosoethanamine
IUPAC
Any carboxylic ester resulting from the formal condensation of a carboxy group with methanol.
carboxylic acid methyl ester
carboxylic acid methyl esters
methyl ester
carboxylic acid methyl ester
ChEBI
carboxylic acid methyl esters
ChEBI
A methanesulfonate ester resulting from the formal condensation of methanesulfonic acid with methanol.
methyl methanesulfonate
CB1540
MMS
Methanesulfonic acid methyl ester
Methyl mesylate
as-Dimethyl sulfite
methyl methanesulfonate
methyl methanesulfonate
IUPAC
CB1540
ChEBI
MMS
ChemIDplus
MMS
KEGG_COMPOUND
Methanesulfonic acid methyl ester
ChemIDplus
Methyl mesylate
ChemIDplus
as-Dimethyl sulfite
ChemIDplus
methylxanthines
methylxanthine
methylxanthines
ChEBI
mitochondrial electron transport chain inhibitors
mitochondrial electron-transport chain inhibitor
mitochondrial respiratory chain inhibitors
mitochondrial respiratory-chain inhibitor
mitochondrial electron transport chain inhibitors
ChEBI
mitochondrial electron-transport chain inhibitor
ChEBI
mitochondrial respiratory chain inhibitors
ChEBI
A family of aziridine-containing natural products isolated from Streptomyces caespitosus or Streptomyces lavendulae.
mitomycins
mitomycin
mitomycins
ChEBI
A molecule all atoms of which have the same atomic number.
homoatomic molecule
homoatomic molecules
elemental molecule
homoatomic molecule
ChEBI
homoatomic molecules
ChEBI
Any polyatomic entity that is an electrically neutral entity consisting of more than one atom.
molecule
Molekuel
molecula
molecules
neutral molecular compounds
molecule
molecule
IUPAC
Molekuel
ChEBI
molecula
IUPAC
molecules
IUPAC
neutral molecular compounds
IUPAC
An oxoacid containing a single carboxy group.
monocarboxylic acids
monocarboxylic acid
monocarboxylic acids
ChEBI
A hydroxybenzoate carrying a single hydroxy substituent at unspecified position.
monohydroxybenzoates
monohydroxybenzoate
monohydroxybenzoates
ChEBI
Any hydroxybenzoic acid having a single phenolic hydroxy substituent on the benzene ring.
monohydroxybenzoic acids
monohydroxybenzoic acid
monohydroxybenzoic acids
ChEBI
Any hydroxynaphthalene derivative that has a single hydroxy substituent.
naphthols
Any fatty acid with one double or triple bond in the fatty acid chain and singly bonded carbon atoms in the rest of the chain. MUFAs have positive effects on the cardiovascular system, and in diabetes treatment.
MUFA
MUFAs
monounsaturated fatty acids
monounsaturated fatty acid
MUFA
ChEBI
MUFAs
ChEBI
monounsaturated fatty acids
ChEBI
monoatomic monocations
monovalent inorganic cations
monoatomic monocation
monoatomic monocations
ChEBI
monovalent inorganic cations
ChEBI
An ethyl sulfide that is diethyl sulfide in which a hydrogen from each of the terminal methyl groups is replaced by a chlorine. It is a powerful vesicant regulated under the Chemical Weapons Convention.
1-chloro-2-[(2-chloroethyl)sulfanyl]ethane
bis(2-chloroethyl) sulfide
1,1'-thiobis(2-chloroethane)
1-chloro-2-[(2-chloroethyl)thio]ethane
Iprit
Lost
Mustard gas
Senfgas
Yperite
bis(2-chloroethyl) sulphide
bis(2-chloroethyl)sulfane
mustard gas
sulfur mustard
bis(2-chloroethyl) sulfide
1-chloro-2-[(2-chloroethyl)sulfanyl]ethane
IUPAC
bis(2-chloroethyl) sulfide
ChemIDplus
1,1'-thiobis(2-chloroethane)
NIST_Chemistry_WebBook
1-chloro-2-[(2-chloroethyl)thio]ethane
IUPAC
Iprit
KEGG_COMPOUND
Lost
NIST_Chemistry_WebBook
Mustard gas
KEGG_COMPOUND
Senfgas
NIST_Chemistry_WebBook
Yperite
NIST_Chemistry_WebBook
bis(2-chloroethyl) sulphide
NIST_Chemistry_WebBook
bis(2-chloroethyl)sulfane
IUPAC
mustard gas
ChemIDplus
sulfur mustard
ChemIDplus
An agent that increases the frequency of mutations above the normal background level, usually by interacting directly with DNA and causing it damage, including base substitution.
mutagene
mutagenes
mutagenic agent
mutageno
mutagenos
mutagens
mutagen
mutagene
ChEBI
mutagenes
ChEBI
mutagenic agent
ChEBI
mutageno
ChEBI
mutagenos
ChEBI
mutagens
ChEBI
Poisonous substance produced by fungi.
fungal toxins
mycotoxins
mycotoxin
fungal toxins
ChEBI
mycotoxins
ChEBI
Any benzenoid aromatic compound having a skeleton composed of two ortho-fused benzene rings.
naphthalenes
A substance used to destroy pests of the phylum Nematoda (roundworms).
nematicides
nematocide
nematocides
nematicide
nematicides
ChEBI
nematocide
ChEBI
nematocides
ChEBI
An epoxycarotenoid that is 6,7-didehydro-5,5',6,6'-tetrahydro-5',6'-epoxy-beta,beta-carotene which is substituted by hydroxy groups at the 3, 3', and 5 positions.
all-trans-Neoxanthin
neoxanthin
all-trans-Neoxanthin
KEGG_COMPOUND
An endogenous compound that is used to transmit information across the synapse between a neuron and another cell.
neurotransmitters
neurotransmitter
neurotransmitters
ChEBI
nickel cation
Ni cation
nickel cations
nickel cation
nickel cation
IUPAC
Ni cation
UniProt
nickel cations
ChEBI
nitrogen
7N
N
Stickstoff
azote
nitrogen
nitrogeno
nitrogen atom
nitrogen
IUPAC
7N
IUPAC
N
IUPAC
Stickstoff
ChEBI
azote
IUPAC
nitrogen
ChEBI
nitrogeno
ChEBI
nonmetal
Nichtmetall
Nichtmetalle
no metal
no metales
non-metal
non-metaux
nonmetal
nonmetals
nonmetal atom
nonmetal
IUPAC
Nichtmetall
ChEBI
Nichtmetalle
ChEBI
no metal
ChEBI
no metales
ChEBI
non-metal
ChEBI
non-metaux
ChEBI
nonmetal
ChEBI
nonmetals
ChEBI
A long-chain, unsaturated fatty acid anion formed by deprotonation of the carboxy group of any octadecadienoic acid; major species at pH 7.3.
octadecadienoate
octadecadienoate
octadecadienoate
IUPAC
Any straight-chain, C18 polyunsaturated fatty acid having two C=C double bonds.
octadecadienoic acid
18:2
C18:2
FA (18:2)
octadecadienoic acid
octadecadienoic acid
IUPAC
18:2
ChEBI
C18:2
ChEBI
FA (18:2)
ChEBI
A fatty acid anion 18:0 that is the conjugate base of octadecanoic acid (stearic acid). Stearates have a variety of uses in the pharmaceutical industry.
octadecanoate
CH3-[CH2]16-COO(-)
Stearate
octadecanoic acid, ion(1-)
stearate
stearic acid, ion(1-)
octadecanoate
octadecanoate
IUPAC
octadecanoate
UniProt
CH3-[CH2]16-COO(-)
IUPAC
Stearate
KEGG_COMPOUND
octadecanoic acid, ion(1-)
ChemIDplus
stearate
ChemIDplus
stearic acid, ion(1-)
ChemIDplus
Any trienoic fatty acid having eighteen carbons.
octadecatrienoic acid
18:3
C18:3
Octadecatriensaeure
octadecatrienoic acid
octadecatrienoic acid
IUPAC
18:3
ChEBI
C18:3
ChEBI
Octadecatriensaeure
ChEBI
Any member of the group of C18 monounsaturated fatty acids with the double bond located at any position in the chain.
octadecenoic acid
octadecenoic acid
octadecenoic acid
IUPAC
A family of polyunsaturated fatty acids that have in common a final carbon-carbon double bond in the omega-3 position, i.e., the third bond from the methyl end of the fatty acid.
omega-3 fatty acid
n-3 fatty acid
n-3 fatty acids
omega-3 fatty acids
omega-3 fatty acid
omega-3 fatty acid
ChEBI
n-3 fatty acid
ChEBI
n-3 fatty acids
ChEBI
omega-3 fatty acids
ChEBI
organic heteromonocyclic compounds
organic heteromonocyclic compound
organic heteromonocyclic compounds
ChEBI
Any organic ion with a net negative charge.
organic anions
organic anion
organic anions
ChEBI
Any organic ion with a net positive charge.
organic cations
organic cation
organic cations
ChEBI
An organooxygen compound with formula ROR, where R is not hydrogen.
ether
ethers
ethers
ether
ether
IUPAC
ethers
IUPAC
ethers
ChEBI
organic ions
organic ion
organic ions
ChEBI
An oxide in which the oxygen atom is bonded to a carbon atom.
organic oxides
organic oxide
organic oxides
ChEBI
Compounds of the general formula SO3HOR where R is an organyl group
organic sulfates
organic sulfate
organic sulfates
ChEBI
An alcohol derived from an aliphatic compound.
Aliphatic alcohol
aliphatic alcohols
an aliphatic alcohol
aliphatic alcohol
Aliphatic alcohol
KEGG_COMPOUND
aliphatic alcohols
ChEBI
an aliphatic alcohol
UniProt
A solute used by a cell under water stress to maintain cell volume.
osmolytes
osmolyte
osmolytes
ChEBI
An oxide is a chemical compound of oxygen with other chemical elements.
oxide
oxides
oxide
oxide
ChEBI
oxides
ChEBI
Any compound that has an aldehydic or ketonic group as well as a carboxylic acid group in the same molecule.
oxo carboxylic acids
oxo acids
oxo carboxylic acids
oxo carboxylic acid
oxo carboxylic acids
IUPAC
oxo acids
IUPAC
oxo carboxylic acids
ChEBI
Any fatty acid anion containing at least one C-C unsaturated bond; formed by deprotonation of the carboxylic acid moiety.
unsaturated fatty acid anion
oxygen
8O
O
Sauerstoff
oxigeno
oxygen
oxygene
oxygen atom
oxygen
IUPAC
8O
IUPAC
O
IUPAC
Sauerstoff
ChEBI
oxigeno
ChEBI
oxygen
ChEBI
oxygene
ChEBI
oxygen molecular entity
oxygen molecular entities
oxygen molecular entity
oxygen molecular entity
ChEBI
oxygen molecular entities
ChEBI
oxopurines
oxopurine
oxopurines
ChEBI
An elemental molecule with formula O3. An explosive, pale blue gas (b.p. -112degreeC) that has a characteristic, pungent odour, it is continuously produced in the upper atmosphere by the action of solar ultraviolet radiation on atmospheric oxygen. It is an antimicrobial agent used in the production of bottled water, as well as in the treatment of meat, poultry and other foodstuffs.
ozone
trioxygen
O3
Ozon
Trisauerstoff
[OO2]
ozono
trioxygene
ozone
ozone
ChEBI
ozone
IUPAC
trioxygen
IUPAC
O3
ChEBI
O3
IUPAC
Ozon
ChEBI
Trisauerstoff
ChEBI
[OO2]
MolBase
ozono
ChEBI
trioxygene
ChEBI
p-N,N-bis(2-chloroethyl)aminophenylvaleric acid
p-N,N-bis(2-chloroethyl)amino-D-phenylalanine
p-N,N-bis(2-chloroethyl)amino-L-phenylalanine
4-(2-aminoethyl)-N,N-bis(2-chloroethyl)aniline
4-(bis(2-chloroethyl)amino)benzeneethanamine
CB 3034
p-(bis(2-chloroethyl)amino)phenethylamine
p-N,N-di-(2-chloroethyl)aminophenylethylamine
4-(2-aminoethyl)-N,N-bis(2-chloroethyl)aniline
4-(2-aminoethyl)-N,N-bis(2-chloroethyl)aniline
IUPAC
4-(bis(2-chloroethyl)amino)benzeneethanamine
ChemIDplus
CB 3034
ChemIDplus
p-(bis(2-chloroethyl)amino)phenethylamine
ChemIDplus
p-N,N-di-(2-chloroethyl)aminophenylethylamine
ChemIDplus
p-p'-N,N-di(2-chloroethyl)aminophenoxyphenylalanine
A quinone in which the two oxo groups of the quinone are located para to each other on the 6-membered quinonoid ring.
p-quinone
para-quinones
p-quinones
p-quinone
ChEBI
para-quinones
ChEBI
A chemically diverse class of peptides that exhibit antimicrobial properties.
peptide antibiotics
peptide antibiotic
peptide antibiotics
ChEBI
Compounds of structure ROOR'.
a peroxide
peroxides
a peroxide
UniProt
Strictly, a substance intended to kill pests. In common usage, any substance used for controlling, preventing, or destroying animal, microbiological or plant pests.
pesticide
Pestizid
Pestizide
pesticides
pesticide
pesticide
IUPAC
Pestizid
ChEBI
Pestizide
ChEBI
pesticides
ChEBI
An amino acid derivative resulting from reaction of alanine at the amino group or the carboxy group, or from the replacement of any hydrogen of phenylalanine by a heteroatom. The definition normally excludes peptides containing phenylalanine residues.
phenylalanine derivative
Any organic aromatic compound with a structure based on a phenylpropane skeleton. The class includes naturally occurring phenylpropanoid esters, flavonoids, anthocyanins, coumarins and many small phenolic molecules as well as their semi-synthetic and synthetic analogues. Phenylpropanoids are also precursors of lignin.
phenylpropanoids
phenylpropanoid
phenylpropanoids
ChEBI
Salts and esters of phosphoric and oligophosphoric acids and their chalcogen analogues. In inorganic chemistry, the term is also used to describe anionic coordination entities with phosphorus as central atom.
phosphates
phosphates
phosphate
phosphates
IUPAC
phosphates
ChEBI
phosphinic acids
phosphite ion
HP(=O)(OH)2 (phosphonic acid) and its P-substituted derivatives.
phosphonic acids
phosphonic acids
phosphonic acids
IUPAC
A phosphorus oxoacid that consists of one oxo and three hydroxy groups joined covalently to a central phosphorus atom.
Phosphoric acid
phosphoric acid
tetraoxophosphoric acid
trihydrogen tetraoxophosphate(3-)
trihydroxidooxidophosphorus
H3PO4
Orthophosphoric acid
Phosphate
Phosphorsaeure
Phosphorsaeureloesungen
[PO(OH)3]
acide phosphorique
acidum phosphoricum
orthophosphoric acid
phosphoric acid
Phosphoric acid
KEGG_COMPOUND
phosphoric acid
IUPAC
tetraoxophosphoric acid
IUPAC
trihydrogen tetraoxophosphate(3-)
IUPAC
trihydroxidooxidophosphorus
IUPAC
H3PO4
IUPAC
Orthophosphoric acid
KEGG_COMPOUND
Phosphate
KEGG_COMPOUND
Phosphorsaeure
ChEBI
Phosphorsaeureloesungen
ChEBI
[PO(OH)3]
IUPAC
acide phosphorique
ChEBI
acidum phosphoricum
ChEBI
orthophosphoric acid
NIST_Chemistry_WebBook
phosphoric acid derivative
phosphorus molecular entities
phosphorus molecular entity
phosphorus molecular entities
ChEBI
photosynthetic electron-transport chain inhibitor
photosystem-II inhibitor
A toxin made by a plant that acts against an organism attacking it.
phytoalexins
phytoalexin
phytoalexins
ChEBI
phytosteroids
phytosteroid
phytosteroids
ChEBI
An endogenous molecular entity that results in a colour of an organism as the consequence of the selective absorption of light.
pigments
biological pigment
pigments
ChEBI
A chemical, natural or artificial, that can affect the rate of growth of a plant.
plant growth regulators
plant growth regulator
plant growth regulators
ChEBI
Any amino acid whose side chain is capable of forming one or more hydrogen bonds.
polar amino acid
polar amino acids
polar amino-acid
polar amino-acids
polar amino acid
polar amino acid
ChEBI
polar amino acids
ChEBI
polar amino-acid
ChEBI
polar amino-acids
ChEBI
A compound that contains two or more hydroxy groups.
polyols
polyol
polyols
ChEBI
polyphenylpropanoid
Any fatty acid containing more than one double bond. Acids in this group are reported to have cardioprotective effects; and levels are lowered in chronic fatigue syndrome.
PUFA
PUFAs
polyunsaturated fatty acids
polyunsaturated fatty acid
PUFA
ChEBI
PUFAs
ChEBI
polyunsaturated fatty acids
ChEBI
Natural pigments containing a fundamental skeleton of four pyrrole nuclei united through the alpha-positions by four methine groups to form a macrocyclic structure.
porphyrins
porphyrins
porphyrins
IUPAC
potassium
19K
K
Kalium
kalium
potasio
potassium
potassium atom
potassium
IUPAC
19K
IUPAC
K
IUPAC
Kalium
ChemIDplus
kalium
IUPAC
potasio
ChEBI
potassium
ChEBI
potassium molecular entity
potassium molecular entities
potassium molecular entity
potassium molecular entity
ChEBI
potassium molecular entities
ChEBI
Any alkali metal salt having potassium(1+) as the cation.
Kaliumsalz
Kaliumsalze
potassium salts
potassium salt
Kaliumsalz
ChEBI
Kaliumsalze
ChEBI
potassium salts
ChEBI
An alpha-amino acid that is pyrrolidine bearing a carboxy substituent at position 2.
proline
DL-Proline
Hpro
Prolin
prolina
pyrrolidine-2-carboxylic acid
proline
proline
ChEBI
proline
IUPAC
DL-Proline
KEGG_COMPOUND
Hpro
IUPAC
Prolin
ChEBI
prolina
ChEBI
pyrrolidine-2-carboxylic acid
IUPAC
Derivatives of oxoacids RnE(=O)OH in which the hydroxy group is replaced by an amino group and the oxo group is replaced by =NR. In organic chemistry an unspecified amidine is commonly a carboxamidine.
amidine
amidines
Amidines
amidines
amidine
amidine
IUPAC
amidines
IUPAC
Amidines
KEGG_COMPOUND
amidines
ChEBI
pteridines
pterins
purine alkaloids
purine alkaloid
purine alkaloids
ChEBI
A nucleobase whose skeleton is derived from purine.
purine nucleobase
a purine nucleobase
purine bases
purine nucleobases
purine nucleobase
purine nucleobase
ChEBI
a purine nucleobase
UniProt
purine bases
ChEBI
purine nucleobases
ChEBI
A class of imidazopyrimidines that consists of purine and its substituted derivatives.
purines
A nucleobase whose skeleton is derived from pyrimidine.
pyrimidine nucleobase
a pyrimidine nucleobase
pyrimidine bases
pyrimidine nucleobases
pyrimidine nucleobase
pyrimidine nucleobase
ChEBI
a pyrimidine nucleobase
UniProt
pyrimidine bases
ChEBI
pyrimidine nucleobases
ChEBI
N-D-Ribosylpyrimidine
pyrimidine nucleosides
pyrimidine nucleoside
N-D-Ribosylpyrimidine
KEGG_COMPOUND
pyrimidine nucleosides
ChEBI
cyclohexa-2,5-diene-1,4-dione--benzene-1,4-diol (1:1)
Chinhydron
green hydroquinone
p-benzoquinhydrone
p-benzoquinone--hydroquinone compound (1:1)
quinhydrone
cyclohexa-2,5-diene-1,4-dione--benzene-1,4-diol (1:1)
IUPAC
Chinhydron
ChemIDplus
green hydroquinone
NIST_Chemistry_WebBook
p-benzoquinhydrone
ChemIDplus
p-benzoquinone--hydroquinone compound (1:1)
NIST_Chemistry_WebBook
A class of aromatic heterocyclic compounds each of which contains a benzene ring ortho fused to carbons 2 and 3 of a pyridine ring.
quinolines
Molecules or ions formed by the incomplete one-electron reduction of oxygen. They contribute to the microbicidal activity of phagocytes, regulation of signal transduction and gene expression, and the oxidative damage to biopolymers.
ROS
reactive oxygen species
ROS
ChEBI
Any compound with a 1,3,5-triazine skeleton, in which nitrogen atoms replace carbon at positions 1, 3 and 5 of the core benzene ring structure.
s-triazines
1,3,5-triazines
s-triazines
ChEBI
Any fatty acid containing no carbon to carbon multiple bonds. Known to produce adverse biological effects when ingested to excess.
saturated fatty acid
SFA
SFAs
saturated fatty acids
saturated fatty acid
saturated fatty acid
ChEBI
SFA
ChEBI
SFAs
ChEBI
saturated fatty acids
ChEBI
An L-alpha-amino acid which is biosynthesised from 3-phosphoglycerate (i.e. serine, glycine, cysteine and homocysteine). A closed class.
3-phosphoglycerate family amino acid
3-phosphoglycerate family amino acids
serine family amino acids
serine family amino acid
3-phosphoglycerate family amino acid
ChEBI
3-phosphoglycerate family amino acids
ChEBI
serine family amino acids
ChEBI
Any terpenoid derived from a sesquiterpene. The term includes compounds in which the C15 skeleton of the parent sesquiterpene has been rearranged or modified by the removal of one or more skeletal atoms (generally methyl groups).
sesquiterpenoides
sesquiterpenoids
sesquiterpenoid
sesquiterpenoides
ChEBI
sesquiterpenoids
ChEBI
An aliphatic monocarboxylic acid with a chain length of less than C6. If any non-hydrocarbon substituent is present, the compound is not normally regarded as a short-chain fatty acid.
SCFA
SCFAs
short-chain fatty acids
short-chain fatty acid
SCFA
ChEBI
SCFAs
ChEBI
short-chain fatty acids
ChEBI
sodium
11Na
Na
Natrium
natrium
sodio
sodium
sodium atom
sodium
IUPAC
11Na
IUPAC
Na
IUPAC
Natrium
ChemIDplus
natrium
IUPAC
sodio
ChemIDplus
sodium
ChEBI
An inorganic sodium salt having hydrogensulfite as the counterion.
sodium hydrogensulfite
NaHSO3
Natriumbisulfit
Natriumhydrogensulfit
primaeres Natriumsulfit
saures Natriumsulfit
sodium bisulfite
sodium bisulphite
sodium hydrogen sulfite
sodium hydrogensulfite
sodium hydrogensulfite
IUPAC
NaHSO3
IUPAC
Natriumbisulfit
ChEBI
Natriumhydrogensulfit
ChEBI
primaeres Natriumsulfit
ChEBI
saures Natriumsulfit
ChEBI
sodium bisulfite
ChemIDplus
sodium bisulphite
ChemIDplus
sodium hydrogen sulfite
ChemIDplus
An inorganic chloride salt having sodium(1+) as the counterion.
sodium chloride
Kochsalz
NaCl
Natriumchlorid
chlorure de sodium
cloruro sodico
common salt
halite
natrii chloridum
rock salt
salt
table salt
sodium chloride
sodium chloride
ChEBI
sodium chloride
IUPAC
Kochsalz
ChEBI
NaCl
IUPAC
Natriumchlorid
NIST_Chemistry_WebBook
chlorure de sodium
ChEBI
cloruro sodico
ChEBI
common salt
ChemIDplus
halite
NIST_Chemistry_WebBook
natrii chloridum
ChEBI
rock salt
ChemIDplus
salt
ChemIDplus
table salt
ChemIDplus
sodium compounds
sodium molecular entities
sodium molecular entity
sodium compounds
ChEBI
sodium molecular entities
ChEBI
Any alkali metal salt having sodium(1+) as the cation.
Natriumsalz
Natriumsalze
sodium salts
sodium salt
Natriumsalz
ChEBI
Natriumsalze
ChEBI
sodium salts
ChEBI
styrylquinoline
An ester of an alcohol and sulfuric acid.
sulfate ester
sulfuric acid ester
sulfuric acid esters
sulfuric ester
sulfate ester
ChEBI
sulfuric acid ester
ChEBI
sulfuric acid esters
ChEBI
Salts and esters of sulfuric acid
sulfates
sulfuric acid derivative
sulphates
sulfates
sulfates
ChEBI
sulfuric acid derivative
ChEBI
sulphates
ChEBI
Any sulfur molecular entity that involves either covalently bonded or anionic sulfur.
sulphides
sulfide
sulphides
ChEBI
Any sulfurous acid derivative that is a salt or an ester of sulfurous acid.
Sulfite
sulfito
sulfitos
sulphites
sulfites
Sulfite
ChEBI
sulfito
ChEBI
sulfitos
ChEBI
sulphites
ChEBI
sulfur
16S
Elemental sulfur
S
Schwefel
azufre
soufre
sulfur
sulphur
theion
sulfur atom
sulfur
IUPAC
16S
IUPAC
Elemental sulfur
KEGG_COMPOUND
S
IUPAC
S
KEGG_COMPOUND
Schwefel
ChEBI
azufre
ChEBI
soufre
ChEBI
sulfur
ChEBI
sulfur
UniProt
sulphur
ChEBI
theion
IUPAC
sulfur-containing amino acids
sulfur-containing amino acid
sulfur-containing amino acids
ChEBI
sulfur molecular entity
sulfur molecular entities
sulfur molecular entity
sulfur molecular entity
ChEBI
sulfur molecular entities
ChEBI
A sulfur oxoacid that consists of two oxo and two hydroxy groups joined covalently to a central sulfur atom.
Sulfuric acid
dihydrogen tetraoxosulfate
dihydroxidodioxidosulfur
hydrogen tetraoxosulfate(2-)
hydrogen tetraoxosulfate(VI)
sulfuric acid
tetraoxosulfuric acid
Acide sulfurique
Acido sulfurico
Acidum sulfuricum
H2SO4
Schwefelsaeureloesungen
[S(OH)2O2]
[SO2(OH)2]
sulphuric acid
sulfuric acid
Sulfuric acid
KEGG_COMPOUND
dihydrogen tetraoxosulfate
IUPAC
dihydroxidodioxidosulfur
IUPAC
hydrogen tetraoxosulfate(2-)
IUPAC
hydrogen tetraoxosulfate(VI)
IUPAC
sulfuric acid
ChEBI
sulfuric acid
IUPAC
tetraoxosulfuric acid
IUPAC
Acide sulfurique
ChemIDplus
Acido sulfurico
ChemIDplus
Acidum sulfuricum
ChemIDplus
H2SO4
IUPAC
Schwefelsaeureloesungen
ChemIDplus
[S(OH)2O2]
MolBase
[SO2(OH)2]
IUPAC
sulphuric acid
MolBase
A synthetic compound exhibiting auxin activity.
synthetic auxins
synthetic auxin
synthetic auxins
ChEBI
Any terpenoid which contains a keto group.
terpene ketone
Any isoprenoid that is a natural product or related compound formally derived from isoprene units. Terpenoids may contain oxygen in various functional groups. This class is subdivided according to the number of carbon atoms in the parent terpene. The skeleton of terpenoids may differ from strict additivity of isoprene units by the loss or shift of a fragment, generally a methyl group.
Terpenoid
terpenoids
terpenoide
terpenoides
terpenoid
Terpenoid
ChEBI
terpenoids
IUPAC
terpenoide
IUPAC
terpenoides
IUPAC
A tertiary alcohol is a compound in which a hydroxy group, -OH, is attached to a saturated carbon atom which has three other carbon atoms attached to it.
tertiary alcohol
tertiary alcohols
tertiary alcohol
tertiary alcohol
ChEBI
tertiary alcohols
ChEBI
Any oxacycle having an oxolane (tetrahydrofuran) skeleton.
oxolanes
A natural pigment containing four pyrrole rings joined by one-carbon units linking position 2 of one pyrrole ring to position 5 of the next.
tetrapyrrole
tetrapyrroles
a tetrapyrrole
tetrapyrrole
tetrapyrrole
IUPAC
tetrapyrroles
IUPAC
a tetrapyrrole
UniProt
Any terpenoid derived from a tetraterpene. The term includes compounds in which the C40 skeleton of the parent tetraterpene has been rearranged or modified by the removal of one or more skeletal atoms (generally methyl groups).
tetraterpenoids
C40 isoprenoids
tetraterpenoides
tetraterpenoid
tetraterpenoids
IUPAC
C40 isoprenoids
LIPID_MAPS
tetraterpenoides
ChEBI
An organic tricyclic compound in which at least one of the rings of the tricyclic skeleton contains one or more heteroatoms.
heterotricyclic compounds
organic heterotricyclic compounds
organic heterotricyclic compound
heterotricyclic compounds
ChEBI
organic heterotricyclic compounds
ChEBI
Any member of the class of benzenes that is a substituted benzene in which the substituents include one (and only one) methyl group.
toluenes
Poisonous substance produced by a biological organism such as a microbe, animal or plant.
toxin
toxins
toxin
toxin
IUPAC
toxins
ChEBI
Any nutrient required in small quantities by organisms throughout their life in order to orchestrate a range of physiological functions.
micronutrients
trace elements
micronutrient
micronutrients
ChEBI
trace elements
ChEBI
An element whose atom has an incomplete d sub-shell, or which can give rise to cations with an incomplete d sub-shell.
transition element
Uebergangselement
Uebergangsmetalle
metal de transicion
metal de transition
metales de transicion
metaux de transition
transition element
transition elements
transition metal
transition metals
transition element atom
transition element
IUPAC
Uebergangselement
ChEBI
Uebergangsmetalle
ChEBI
metal de transicion
ChEBI
metal de transition
ChEBI
metales de transicion
ChEBI
metaux de transition
ChEBI
transition element
ChEBI
transition elements
ChEBI
transition metal
ChEBI
transition metals
ChEBI
A member of the class of 1,4-benzoquinones that is 1,4-benzoquinone in which three of the ring hydrogens are replaced by aziridin-1-yl groups.
2,3,5-tris(aziridin-1-yl)-1,4-benzoquinone
1,1',1''-(3,6-Dioxo-1,4-cyclohexadiene-1,2,4-triyl)trisaziridine
2,3,5-Ethylenimine-1,4-benzoquinone
2,3,5-Tri(1-aziridinyl)-p-benzoquinone
2,3,5-Tri-(1-aziridinyl)-p-benzoquinone
2,3,5-Triethyleneimino-1,4-benzoquinone
2,3,5-Tris(1-aziridino)-p-benzoquinone
2,3,5-Tris(1-aziridinyl)-2,5-cyclohexadiene-1,4-dione
2,3,5-Tris(1-aziridinyl)-p-benzoquinone
2,3,5-Tris(aziridino)-1,4-benzoquinone
2,3,5-Tris(ethyleneimino)-1,4-benzoquinone
2,3,5-Tris(ethylenimino)-1,4-benzoquinone
2,3,5-Tris(ethylenimino)-p-benzoquinone
2,3,5-Tris(ethylenimino)benzoquinone
2,3,5-Trisethyleneiminobenzoquinone
Triazichon
Triaziquonum
Triethyleneaminobenzoquinone
Tris(1-aziridinyl)-p-benzoquinone
Tris(aziridinyl)-p-benzoquinone
Tris(aziridinyl)-para-benzoquinone
Tris(ethyleneimino)benzoquinone
triazicuona
triaziquone
triaziquone
2,3,5-tris(aziridin-1-yl)-1,4-benzoquinone
IUPAC
1,1',1''-(3,6-Dioxo-1,4-cyclohexadiene-1,2,4-triyl)trisaziridine
ChemIDplus
2,3,5-Ethylenimine-1,4-benzoquinone
NIST_Chemistry_WebBook
2,3,5-Tri(1-aziridinyl)-p-benzoquinone
NIST_Chemistry_WebBook
2,3,5-Tri-(1-aziridinyl)-p-benzoquinone
ChemIDplus
2,3,5-Triethyleneimino-1,4-benzoquinone
ChemIDplus
2,3,5-Tris(1-aziridino)-p-benzoquinone
ChemIDplus
2,3,5-Tris(1-aziridinyl)-2,5-cyclohexadiene-1,4-dione
NIST_Chemistry_WebBook
2,3,5-Tris(1-aziridinyl)-p-benzoquinone
ChemIDplus
2,3,5-Tris(aziridino)-1,4-benzoquinone
ChemIDplus
2,3,5-Tris(ethyleneimino)-1,4-benzoquinone
ChemIDplus
2,3,5-Tris(ethylenimino)-1,4-benzoquinone
ChemIDplus
2,3,5-Tris(ethylenimino)-p-benzoquinone
ChemIDplus
2,3,5-Tris(ethylenimino)benzoquinone
ChemIDplus
2,3,5-Trisethyleneiminobenzoquinone
ChemIDplus
Triazichon
ChemIDplus
Triaziquonum
ChemIDplus
Triethyleneaminobenzoquinone
ChemIDplus
Tris(1-aziridinyl)-p-benzoquinone
ChemIDplus
Tris(aziridinyl)-p-benzoquinone
NIST_Chemistry_WebBook
Tris(aziridinyl)-para-benzoquinone
KEGG_COMPOUND
Tris(ethyleneimino)benzoquinone
ChemIDplus
triazicuona
ChemIDplus
triaziquone
KEGG_DRUG
triaziquone
WHO_MedNet
trimethylxanthines
trimethylxanthine
trimethylxanthines
ChEBI
A chemical compound containing three hydroxy groups.
triols
triol
triols
ChEBI
trisaccharides
trisaccharide
trisaccharides
ChEBI
An amino acid derivative resulting from reaction of tryptophan at the amino group or the carboxy group, or from the replacement of any hydrogen of tryptophan by a heteroatom. The definition normally excludes peptides containing tryptophan residues.
tryptophan derivatives
tryptophan derivative
tryptophan derivatives
ChEBI
heterobicyclic compounds
organic heterobicyclic compounds
organic heterobicyclic compound
heterobicyclic compounds
ChEBI
organic heterobicyclic compounds
ChEBI
A univalent carboacyl group is a group formed by loss of OH from the carboxy group of a carboxylic acid.
univalent acyl group
univalent carboacyl groups
univalent carboxylic acyl groups
univalent carboacyl group
univalent acyl group
ChEBI
univalent carboacyl groups
ChEBI
univalent carboxylic acyl groups
ChEBI
Any fatty acid containing at least one C=C or C#C bond.
alkene acid
olefinic acid
unsaturated fatty acids
unsaturated fatty acid
alkene acid
ChEBI
olefinic acid
ChEBI
unsaturated fatty acids
ChEBI
unsaturated fatty acids
LIPID_MAPS
uridines
vinyl carbamate
carbamic acid, vinyl ester
ethenyl carbamate
vinyl carbamate
vinyl carbamate
IUPAC
carbamic acid, vinyl ester
ChemIDplus
ethenyl carbamate
ChemIDplus
An epoxycarotenol that is 5,5',6,6'-tetrahydro-5,6:5',6'-diepoxy-beta,beta-carotene substituted by hydroxy groups at positions 3 and 3'. It is the naturally occurring xanthophyll pigment found in a variety of plants.
violaxanthin
Any plant metabolite that is found naturally as a component of a volatile oil.
essential oil component
essential oil components
ethereal oil component
ethereal oil components
volatile oil components
volatile oil component
essential oil component
ChEBI
essential oil components
ChEBI
ethereal oil component
ChEBI
ethereal oil components
ChEBI
volatile oil components
ChEBI
Any vitamin that dissolves in water and readily absorbed into tissues for immediate use. Unlike the fat-soluble vitamins, they are not stored in the body and need to be replenished regularly in the diet and will rarely accumulate to toxic levels since they are quickly excreted from the body via urine.
wasserloesliche Vitamine
water-soluble vitamin
water-soluble vitamins
water-soluble vitamin (role)
wasserloesliche Vitamine
ChEBI
water-soluble vitamin
ChEBI
water-soluble vitamins
ChEBI
A subclass of carotenoids consisting of the oxygenated carotenes.
xanthophylls
xanthophylls
xanthophyll
xanthophylls
IUPAC
xanthophylls
ChEBI
zinc
30Zn
Zink
Zn
Zn(II)
Zn2+
cinc
zinc
zincum
zinc atom
zinc
IUPAC
30Zn
IUPAC
Zink
ChEBI
Zn
IUPAC
Zn(II)
KEGG_COMPOUND
Zn2+
KEGG_COMPOUND
cinc
ChEBI
zinc
ChEBI
zincum
ChEBI
zinc compounds
zinc molecular entities
zinc molecular entity
zinc compounds
ChEBI
zinc molecular entities
ChEBI
zinc ion
zinc ions
zinc ion
zinc ion
ChEBI
zinc ions
ChEBI
A neutral compound having formal unit electrical charges of opposite sign on non-adjacent atoms. Sometimes referred to as inner salts, dipolar ions (a misnomer).
zwitterion
zwitterions
compose zwitterionique
compuestos zwitterionicos
zwitteriones
zwitterionic compounds
zwitterion
zwitterion
IUPAC
zwitterions
IUPAC
compose zwitterionique
IUPAC
compuestos zwitterionicos
IUPAC
zwitteriones
IUPAC
zwitterionic compounds
IUPAC
An alkanesulfonic acid in which the alkyl group directly linked to the sulfo functionality is methyl.
Methanesulfonic acid
methanesulfonic acid
Methansulfonsaeure
methylsulfonic acid
methanesulfonic acid
Methanesulfonic acid
KEGG_COMPOUND
methanesulfonic acid
IUPAC
Methansulfonsaeure
ChEBI
methylsulfonic acid
NIST_Chemistry_WebBook
A member of the class of 6-aminopurines that is adenine carrying a (furan-2-ylmethyl) substituent at the exocyclic amino group.
N-(furan-2-ylmethyl)-7H-purin-6-amine
kinetin
6-(furfurylamino)purine
6-furfuryladenine
N(6)-(furfurylamino)purine
N(6)-furfuryladenine
N-furfuryladenine
kinetin
N-(furan-2-ylmethyl)-7H-purin-6-amine
IUPAC
kinetin
ChemIDplus
kinetin
UniProt
6-(furfurylamino)purine
ChemIDplus
6-furfuryladenine
ChemIDplus
N(6)-(furfurylamino)purine
ChemIDplus
N(6)-furfuryladenine
ChemIDplus
N-furfuryladenine
ChemIDplus
A linolenic acid with cis-double bonds at positions 9, 12 and 15. Shown to have an antithrombotic effect.
(9Z,12Z,15Z)-octadeca-9,12,15-trienoic acid
ALPHA-LINOLENIC ACID
alpha-Linolenic acid
alpha-linolenic acid
(9,12,15)-linolenic acid
(9Z,12Z,15Z)-Octadecatrienoic acid
(Z,Z,Z)-9,12,15-octadecatrienoic acid
9,12,15-Octadecatrienoic acid
9-cis,12-cis,15-cis-octadecatrienoic acid
ALA
all-cis-9,12,15-octadecatrienoic acid
cis,cis,cis-9,12,15-octadecatrienoic acid
cis-Delta(9,12,15)-octadecatrienoic acid
linolenic acid
alpha-linolenic acid
(9Z,12Z,15Z)-octadeca-9,12,15-trienoic acid
IUPAC
ALPHA-LINOLENIC ACID
PDBeChem
alpha-Linolenic acid
KEGG_COMPOUND
alpha-linolenic acid
NIST_Chemistry_WebBook
(9,12,15)-linolenic acid
CBN
(9Z,12Z,15Z)-Octadecatrienoic acid
KEGG_COMPOUND
(Z,Z,Z)-9,12,15-octadecatrienoic acid
NIST_Chemistry_WebBook
9,12,15-Octadecatrienoic acid
KEGG_COMPOUND
9-cis,12-cis,15-cis-octadecatrienoic acid
ChemIDplus
ALA
ChEBI
all-cis-9,12,15-octadecatrienoic acid
NIST_Chemistry_WebBook
cis,cis,cis-9,12,15-octadecatrienoic acid
NIST_Chemistry_WebBook
cis-Delta(9,12,15)-octadecatrienoic acid
ChemIDplus
linolenic acid
ChEBI
An N-acyl-amino acid that is a form of the water-soluble vitamin B9. Its biologically active forms (tetrahydrofolate and others) are essential for nucleotide biosynthesis and homocysteine remethylation.
N-(4-{[(2-amino-4-oxo-3,4-dihydropteridin-6-yl)methyl]amino}benzoyl)-L-glutamic acid
(2S)-2-(4-{[(2-amino-4-oxo-3,4-dihydropteridin-6-yl)methyl]amino}benzamido)pentanedioic acid
Acfol
Folate
Folicet
Folsaeure
N-[(4-{[(2-amino-4-oxo-1,4-dihydropteridin-6-yl)methyl]amino}phenyl)carbonyl]-L-glutamic acid
N-pteroyl-L-glutamic acid
PGA
PteGlu
acide folique
acido folico
acidum folicum
folic acid
pteroyl-L-glutamic acid
pteroyl-L-monoglutamic acid
pteroylglutamic acid
pteroylmonoglutamic acid
vitamin B11
vitamin B9
vitamin Bc
vitamin Be
vitamin M
folic acid
N-(4-{[(2-amino-4-oxo-3,4-dihydropteridin-6-yl)methyl]amino}benzoyl)-L-glutamic acid
IUPAC
(2S)-2-(4-{[(2-amino-4-oxo-3,4-dihydropteridin-6-yl)methyl]amino}benzamido)pentanedioic acid
IUPAC
Acfol
ChemIDplus
Folate
KEGG_COMPOUND
Folicet
KEGG_DRUG
Folsaeure
ChEBI
N-[(4-{[(2-amino-4-oxo-1,4-dihydropteridin-6-yl)methyl]amino}phenyl)carbonyl]-L-glutamic acid
PDBeChem
N-pteroyl-L-glutamic acid
ChEBI
PGA
NIST_Chemistry_WebBook
PteGlu
NIST_Chemistry_WebBook
acide folique
WHO_MedNet
acido folico
WHO_MedNet
acidum folicum
WHO_MedNet
folic acid
WHO_MedNet
pteroyl-L-glutamic acid
ChemIDplus
pteroyl-L-monoglutamic acid
ChemIDplus
pteroylglutamic acid
KEGG_COMPOUND
pteroylmonoglutamic acid
ChemIDplus
vitamin B11
ChemIDplus
vitamin B9
ChemIDplus
vitamin Bc
ChemIDplus
vitamin Be
ChemIDplus
vitamin M
ChemIDplus
Mitomycin C
[(1aS,8S,8aR,8bS)-6-amino-8a-methoxy-5-methyl-4,7-dioxo-1,1a,2,4,7,8,8a,8b-octahydroazirino[2',3':3,4]pyrrolo[1,2-a]indol-8-yl]methyl carbamate
7-Amino-9alpha-methoxymitosane
Ametycine
MMC
Mitocin-C
Mitomycin
Mutamycin
mitomycin C
Mitomycin C
KEGG_COMPOUND
[(1aS,8S,8aR,8bS)-6-amino-8a-methoxy-5-methyl-4,7-dioxo-1,1a,2,4,7,8,8a,8b-octahydroazirino[2',3':3,4]pyrrolo[1,2-a]indol-8-yl]methyl carbamate
IUPAC
7-Amino-9alpha-methoxymitosane
ChemIDplus
Ametycine
ChemIDplus
MMC
ChemIDplus
Mitocin-C
ChemIDplus
Mitomycin
KEGG_COMPOUND
Mutamycin
ChemIDplus
(3R,3'R)-beta,beta-carotene-3,3'-diol
Zeaxanthin
(3R,3'R)-dihydroxy-beta,beta-carotene
all-trans-beta-carotene-3,3'-diol
all-trans-zeaxanthin
anchovyxanthin
beta,beta-carotene-3,3'-diol
zeaxanthin
(3R,3'R)-beta,beta-carotene-3,3'-diol
IUPAC
Zeaxanthin
KEGG_COMPOUND
(3R,3'R)-dihydroxy-beta,beta-carotene
ChEBI
all-trans-beta-carotene-3,3'-diol
ChEBI
all-trans-zeaxanthin
UniProt
anchovyxanthin
ChEBI
beta,beta-carotene-3,3'-diol
ChEBI
boron
5B
B
Bor
Boron
boracium
bore
boro
boron
boron atom
boron
IUPAC
5B
IUPAC
B
KEGG_COMPOUND
Bor
ChEBI
Boron
KEGG_COMPOUND
boracium
ChEBI
bore
ChEBI
boro
ChEBI
boron
ChEBI
A saturated organic heteromonocyclic parent that is a three-membered heterocycle of two carbon atoms and one oxygen atom.
oxirane
1,2-Epoxyaethan
1,2-epoxyethane
Aethylenoxid
Amprolene
Anprolene
Anproline
Dihydrooxirene
Dimethylene oxide
ETO
Ethylene oxide
Oxacyclopropane
Oxane
Oxidoethane
Oxyfume
epoxyethane
ethene oxide
oxyde d'ethylene
oxirane
oxirane
IUPAC
1,2-Epoxyaethan
ChemIDplus
1,2-epoxyethane
NIST_Chemistry_WebBook
Aethylenoxid
ChemIDplus
Amprolene
ChemIDplus
Anprolene
NIST_Chemistry_WebBook
Anproline
ChemIDplus
Dihydrooxirene
ChemIDplus
Dimethylene oxide
ChemIDplus
ETO
ChemIDplus
Ethylene oxide
KEGG_COMPOUND
Oxacyclopropane
ChemIDplus
Oxane
ChemIDplus
Oxidoethane
ChemIDplus
Oxyfume
ChEBI
epoxyethane
NIST_Chemistry_WebBook
ethene oxide
NIST_Chemistry_WebBook
oxyde d'ethylene
ChemIDplus
arsenic
33As
Arsen
Arsenic
As
arsenic
arsenico
arsenicum
arsenic atom
arsenic
IUPAC
33As
IUPAC
Arsen
ChemIDplus
Arsenic
KEGG_COMPOUND
As
KEGG_COMPOUND
arsenic
ChEBI
arsenico
ChEBI
arsenicum
ChEBI
selenium
34Se
Se
Selen
Selenium
selenio
selenium
selenium atom
selenium
IUPAC
34Se
IUPAC
Se
IUPAC
Selen
ChemIDplus
Selenium
KEGG_COMPOUND
selenio
ChEBI
selenium
ChEBI
silicon
14Si
Si
Silicon
Silizium
silicio
silicium
silicon
silicon atom
silicon
IUPAC
14Si
IUPAC
Si
IUPAC
Si
KEGG_COMPOUND
Silicon
KEGG_COMPOUND
Silizium
ChEBI
silicio
ChEBI
silicium
ChEBI
silicon
ChEBI
carbon
6C
C
Carbon
Kohlenstoff
carbon
carbone
carbonium
carbono
carbon atom
carbon
IUPAC
6C
IUPAC
C
IUPAC
C
KEGG_COMPOUND
Carbon
KEGG_COMPOUND
Kohlenstoff
ChEBI
carbon
ChEBI
carbone
ChEBI
carbonium
ChEBI
carbono
ChEBI
A cobalt group element atom that has atomic number 27.
cobalt
27Co
Co
Cobalt
Kobalt
cobalt
cobalto
cobaltum
cobalt atom
cobalt
IUPAC
27Co
IUPAC
Co
IUPAC
Co
UniProt
Cobalt
KEGG_COMPOUND
Kobalt
NIST_Chemistry_WebBook
cobalt
ChEBI
cobalto
ChEBI
cobaltum
ChEBI
2-amino-4,6-dimethyl-3-oxo-1-N,9-N-bis-[(18aS)-10c,14,17-trimethyl-5,8,12,15,18-pentaoxo-6c,13t-di(propan-2-yl)-18ar-hexadecahydro-1H-pyrrolo[2,1-i][1,4,7,10,13]oxatetraazacyclohexadecin-9c-yl]-3H-phenoxazine-1,9-dicarboxamide
Actinomycin D
2-amino-N,N'-bis(hexadecahydro-2,5,9-trimethyl-6,13-bis(1-methylethyl)-1,4,7,11,14-pentaoxo-1H-pyrrolo(2,1-i)(1,4,7,10,13)oxatetra-azacyclohexadecin-10-yl)-4,6-dimethyl-3-oxo-3H-phenoxazine-1,9-dicarboxamide
ActD
Dactinomycin
actinomycin C1
actinomycin IV
actinomycin D
2-amino-4,6-dimethyl-3-oxo-1-N,9-N-bis-[(18aS)-10c,14,17-trimethyl-5,8,12,15,18-pentaoxo-6c,13t-di(propan-2-yl)-18ar-hexadecahydro-1H-pyrrolo[2,1-i][1,4,7,10,13]oxatetraazacyclohexadecin-9c-yl]-3H-phenoxazine-1,9-dicarboxamide
IUPAC
Actinomycin D
KEGG_COMPOUND
2-amino-N,N'-bis(hexadecahydro-2,5,9-trimethyl-6,13-bis(1-methylethyl)-1,4,7,11,14-pentaoxo-1H-pyrrolo(2,1-i)(1,4,7,10,13)oxatetra-azacyclohexadecin-10-yl)-4,6-dimethyl-3-oxo-3H-phenoxazine-1,9-dicarboxamide
ChemIDplus
ActD
ChEBI
Dactinomycin
KEGG_COMPOUND
actinomycin C1
ChEBI
actinomycin IV
ChemIDplus
A trimethylxanthine in which the three methyl groups are located at positions 1, 3, and 7. A purine alkaloid that occurs naturally in tea and coffee.
1,3,7-trimethyl-3,7-dihydro-1H-purine-2,6-dione
CAFFEINE
Caffeine
caffeine
1,3,7-Trimethylxanthine
1,3,7-trimethyl-2,6-dioxopurine
1,3,7-trimethylpurine-2,6-dione
1,3,7-trimethylxanthine
1-methyltheobromine
3,7-Dihydro-1,3,7-trimethyl-1H-purin-2,6-dion
7-methyltheophylline
Coffein
Koffein
Thein
anhydrous caffeine
cafeina
cafeine
guaranine
mateina
methyltheobromine
teina
theine
caffeine
1,3,7-trimethyl-3,7-dihydro-1H-purine-2,6-dione
IUPAC
CAFFEINE
PDBeChem
Caffeine
KEGG_COMPOUND
caffeine
UniProt
1,3,7-Trimethylxanthine
KEGG_COMPOUND
1,3,7-trimethyl-2,6-dioxopurine
ChemIDplus
1,3,7-trimethylpurine-2,6-dione
IUPHAR
1,3,7-trimethylxanthine
NIST_Chemistry_WebBook
1-methyltheobromine
ChemIDplus
3,7-Dihydro-1,3,7-trimethyl-1H-purin-2,6-dion
NIST_Chemistry_WebBook
7-methyltheophylline
NIST_Chemistry_WebBook
Coffein
ChemIDplus
Koffein
ChemIDplus
Thein
ChemIDplus
anhydrous caffeine
KEGG_DRUG
cafeina
ChemIDplus
cafeine
ChEBI
guaranine
IUPHAR
mateina
ChemIDplus
methyltheobromine
IUPHAR
teina
ChEBI
theine
NIST_Chemistry_WebBook
Any hydroxyflavone with a hydroxy substituent at position 3'.
3'-Hydroxyflavonoid
3'-hydroxyflavones
3'-hydroxyflavonoids
a 3'-hydroxyflavone
3'-hydroxyflavonoid
3'-Hydroxyflavonoid
KEGG_COMPOUND
3'-hydroxyflavones
ChEBI
3'-hydroxyflavonoids
ChEBI
a 3'-hydroxyflavone
UniProt
A phosphonic acid resulting from the formal oxidative coupling of the methyl group of methylphosphonic acid with the amino group of glycine. It is one of the most commonly used herbicides worldwide, and the only one to target the enzyme 5-enolpyruvyl-3-shikimate phosphate synthase (EPSPS).
Glyphosate
N-(phosphonomethyl)glycine
Roundup
glyphosate
Glyphosate
KEGG_COMPOUND
N-(phosphonomethyl)glycine
IUPAC
Roundup
KEGG_COMPOUND
A surfactant (or a mixture containing one or more surfactants) having cleaning properties in dilute solutions.
detergent
Detergents
detergent
detergent
IUPAC
Detergents
KEGG_COMPOUND
A member of the class of chloroethanes substituted by two chloro groups at positions 1 and 2.
1,2-DICHLOROETHANE
1,2-Dichloroethane
1,2-dichloroethane
1,2-DCE
1,2-Dichloraethan
Aethylenchlorid
Aethylendichlorid
DCE
Dutch liquid
EDC
Ethylene dichloride
Glycol dichloride
alpha,beta-dichloroethane
ethane dichloride
ethylene chloride
1,2-dichloroethane
1,2-DICHLOROETHANE
PDBeChem
1,2-Dichloroethane
KEGG_COMPOUND
1,2-dichloroethane
IUPAC
1,2-dichloroethane
UniProt
1,2-DCE
NIST_Chemistry_WebBook
1,2-Dichloraethan
ChEBI
Aethylenchlorid
ChEBI
Aethylendichlorid
ChEBI
DCE
ChemIDplus
Dutch liquid
KEGG_COMPOUND
EDC
ChemIDplus
Ethylene dichloride
KEGG_COMPOUND
Glycol dichloride
KEGG_COMPOUND
alpha,beta-dichloroethane
NIST_Chemistry_WebBook
ethane dichloride
ChemIDplus
ethylene chloride
ChemIDplus
CHLOROPHYLL B
Chlorophyll b
[methyl (3S,4S,21R)-9-ethenyl-14-ethyl-13-formyl-4,8,18-trimethyl-20-oxo-3-(3-oxo-3-{[(2E,7R,11R)-3,7,11,15-tetramethylhexadec-2-en-1-yl]oxy}propyl)phorbine-21-carboxylatato(2-)-kappa(4)N(23),N(24),N(25),N(26)]magnesium
chlorophyll b
(SP-4-2)-((2E,7R,11R)-3,7,11,15-tetramethyl-2-hexadecenyl (3S,4S,21R)-9-ethenyl-14-ethyl-13-formyl-21-(methoxycarbonyl)-4,8,18-trimethyl-20-oxo-3-phorbinepropanoato(2-)-kappaN(23),kappaN(24),kappaN(25),kappaN(26))-magnesium
chlorophyll b
CHLOROPHYLL B
PDBeChem
Chlorophyll b
KEGG_COMPOUND
[methyl (3S,4S,21R)-9-ethenyl-14-ethyl-13-formyl-4,8,18-trimethyl-20-oxo-3-(3-oxo-3-{[(2E,7R,11R)-3,7,11,15-tetramethylhexadec-2-en-1-yl]oxy}propyl)phorbine-21-carboxylatato(2-)-kappa(4)N(23),N(24),N(25),N(26)]magnesium
IUPAC
chlorophyll b
JCBN
(SP-4-2)-((2E,7R,11R)-3,7,11,15-tetramethyl-2-hexadecenyl (3S,4S,21R)-9-ethenyl-14-ethyl-13-formyl-21-(methoxycarbonyl)-4,8,18-trimethyl-20-oxo-3-phorbinepropanoato(2-)-kappaN(23),kappaN(24),kappaN(25),kappaN(26))-magnesium
ChemIDplus
An alpha-amino acid that is alanine bearing an indol-3-yl substituent at position 3.
Tryptophan
tryptophan
2-amino-3-(1H-indol-3-yl)propanoic acid
Htrp
Trp
W
alpha-Amino-beta-(3-indolyl)-propionic acid
alpha-amino-beta-3-indolepropionic acid
beta-3-indolylalanine
triptofano
tryptophane
tryptophan
Tryptophan
KEGG_COMPOUND
tryptophan
IUPAC
2-amino-3-(1H-indol-3-yl)propanoic acid
IUPAC
Htrp
IUPAC
Trp
ChEBI
W
ChEBI
alpha-Amino-beta-(3-indolyl)-propionic acid
KEGG_COMPOUND
alpha-amino-beta-3-indolepropionic acid
ChEBI
beta-3-indolylalanine
ChEBI
triptofano
ChEBI
tryptophane
ChEBI
A diamminedichloroplatinum compound in which the two ammine ligands and two chloro ligands are oriented in a cis planar configuration around the central platinum ion. An anticancer drug that interacts with, and forms cross-links between, DNA and proteins, it is used as a neoplasm inhibitor to treat solid tumours, primarily of the testis and ovary. Commonly but incorrectly described as an alkylating agent due to its mechanism of action (but it lacks alkyl groups).
(SP-4-2)-diamminedichloridoplatinum
(SP-4-2)-diamminedichloroplatinum
Cisplatin
cis-diamminedichloridoplatinum(II)
cis-diamminedichloroplatinum(II)
Briplatin
CDDP
Cismaplat
Lederplatin
Neoplatin
Peyrone's chloride
Peyrone's salt
Platamine
Platinex
Platinol
Randa
[PtCl2(NH3)2]
cis-DDP
cis-Diamminedichloroplatinum(II)
cis-[PtCl2(NH3)2]
cis-diamminedichloroplatinum
cis-diammineplatinum(II) dichloride
cis-dichlorodiammineplatinum(II)
cis-platin
cisplatin
cisplatine
cisplatino
cisplatinum
cisplatin
(SP-4-2)-diamminedichloridoplatinum
IUPAC
(SP-4-2)-diamminedichloroplatinum
IUPAC
Cisplatin
KEGG_COMPOUND
cis-diamminedichloridoplatinum(II)
IUPAC
cis-diamminedichloroplatinum(II)
IUPAC
Briplatin
ChemIDplus
CDDP
KEGG_COMPOUND
Cismaplat
DrugBank
Lederplatin
DrugBank
Neoplatin
DrugBank
Peyrone's chloride
ChemIDplus
Peyrone's salt
ChEBI
Platamine
DrugBank
Platinex
DrugBank
Platinol
KEGG_DRUG
Randa
DrugBank
[PtCl2(NH3)2]
KEGG_COMPOUND
cis-DDP
ChemIDplus
cis-Diamminedichloroplatinum(II)
KEGG_COMPOUND
cis-[PtCl2(NH3)2]
MolBase
cis-diamminedichloroplatinum
ChemIDplus
cis-diammineplatinum(II) dichloride
ChemIDplus
cis-dichlorodiammineplatinum(II)
ChemIDplus
cis-platin
ChEBI
cisplatin
ChemIDplus
cisplatine
ChemIDplus
cisplatino
ChemIDplus
cisplatinum
ChemIDplus
2,4,6-tri(aziridin-1-yl)-1,3,5-triazine
tretamine
2,4,6-tri(1-aziridinyl)-1,3,5-triazine
2,4,6-tris(1-aziridinyl)-1,3,5-triazine
2,4,6-tris(1-aziridinyl)-s-triazine
2,4,6-tris(aziridin-1-yl)-1,3,5-triazine
TEM
Triethylenemelamine
Trisaziridinyltriazine
tretamine
2,4,6-tri(aziridin-1-yl)-1,3,5-triazine
IUPAC
tretamine
ChemIDplus
2,4,6-tri(1-aziridinyl)-1,3,5-triazine
NIST_Chemistry_WebBook
2,4,6-tris(1-aziridinyl)-1,3,5-triazine
NIST_Chemistry_WebBook
2,4,6-tris(1-aziridinyl)-s-triazine
NIST_Chemistry_WebBook
2,4,6-tris(aziridin-1-yl)-1,3,5-triazine
ChEBI
TEM
ChEBI
Triethylenemelamine
KEGG_COMPOUND
Trisaziridinyltriazine
KEGG_COMPOUND
The most important reserve polysaccharide found in plants. It is a glucan consisting of amylose and amylopectin.
Starch
Staerke
amidon
amylum
starch
Starch
KEGG_COMPOUND
Staerke
ChEBI
amidon
ChEBI
amylum
ChEBI
An aromatic amino acid that is alanine in which one of the methyl hydrogens is substituted by a phenyl group.
2-amino-3-phenylpropanoic acid
Phenylalanine
phenylalanine
DL-Phenylalanine
F
PHE
Phenylalanin
alpha-Amino-beta-phenylpropionic acid
fenilalanina
phenylalanine
2-amino-3-phenylpropanoic acid
IUPAC
Phenylalanine
KEGG_COMPOUND
phenylalanine
ChEBI
phenylalanine
IUPAC
DL-Phenylalanine
KEGG_COMPOUND
F
ChEBI
PHE
ChEBI
Phenylalanin
ChEBI
alpha-Amino-beta-phenylpropionic acid
KEGG_COMPOUND
fenilalanina
ChEBI
A polydisperse highly branched polysaccharide derivative composed of chains of D-glucopyranose residues in alpha(1->4) glycosidic linkage. The chains are joined together by alpha(1->6) glycosidic linkages. A small number of alpha(1->3) glycosidic linkages and some 6-phosphate ester groups also may occur. The branches in amylopectin typically contain 24 to 30 glucose residues.
Amylopectin
amylopectin
Amylopectin
KEGG_COMPOUND
A chromium group element atom that has atomic number 24.
chromium
24Cr
Chrom
Chromium
Cr
chrome
chromium
cromo
chromium atom
chromium
IUPAC
24Cr
IUPAC
Chrom
ChemIDplus
Chromium
KEGG_COMPOUND
Cr
IUPAC
Cr
KEGG_COMPOUND
chrome
ChEBI
chromium
ChEBI
cromo
ChEBI
A glucan composed of unbranched chains of D-glucopyranose residues in alpha(1->4) glycosidic linkage. The number of repeated glucose subunits (n) is usually in the range of 300 to 3000, but can be many thousands. One of the two components of starch (the other, 70-80%, being amylopectin). Cf. linear maltodextrin, in which the chain length is typically between 3 and 17 glucose units.
(1->4)-alpha-D-glucopyranan
Amylose
(1,4-alpha-D-Glucosyl)n
(1,4-alpha-D-Glucosyl)n+1
(1,4-alpha-D-Glucosyl)n-1
1,4-alpha-D-Glucan
4-{(1,4)-alpha-D-Glucosyl}(n-1)-D-glucose
Amylose chain
amylose
(1->4)-alpha-D-glucopyranan
IUPAC
Amylose
KEGG_COMPOUND
(1,4-alpha-D-Glucosyl)n
KEGG_COMPOUND
(1,4-alpha-D-Glucosyl)n+1
KEGG_COMPOUND
(1,4-alpha-D-Glucosyl)n-1
KEGG_COMPOUND
1,4-alpha-D-Glucan
KEGG_COMPOUND
4-{(1,4)-alpha-D-Glucosyl}(n-1)-D-glucose
KEGG_COMPOUND
Amylose chain
KEGG_COMPOUND
Chemical element (nickel group element atom) with atomic number 28.
nickel
28Ni
Ni
Nickel
Raney alloy
niccolum
nickel
niquel
nickel atom
nickel
IUPAC
28Ni
IUPAC
Ni
IUPAC
Ni
UniProt
Nickel
ChEBI
Raney alloy
ChemIDplus
niccolum
ChEBI
nickel
ChEBI
niquel
ChEBI
A 2-carbon sulfoxide in which the sulfur atom has two methyl substituents.
(methanesulfinyl)methane
DIMETHYL SULFOXIDE
Dimethyl sulfoxide
dimethyl sulfoxide
(CH3)2SO
DMSO
Dimethylsulfoxid
S(O)Me2
dimethyl sulfoxide
dimethyl sulfur oxide
dimethyl sulphoxide
dimethyli sulfoxidum
dimethylsulfoxyde
dimetil sulfoxido
dmso
methylsulfinylmethane
sulfinylbis(methane)
dimethyl sulfoxide
(methanesulfinyl)methane
IUPAC
DIMETHYL SULFOXIDE
PDBeChem
Dimethyl sulfoxide
KEGG_COMPOUND
dimethyl sulfoxide
IUPAC
dimethyl sulfoxide
UniProt
(CH3)2SO
NIST_Chemistry_WebBook
DMSO
KEGG_COMPOUND
Dimethylsulfoxid
ChEBI
S(O)Me2
ChEBI
dimethyl sulfoxide
ChemIDplus
dimethyl sulfur oxide
NIST_Chemistry_WebBook
dimethyl sulphoxide
ChemIDplus
dimethyli sulfoxidum
ChemIDplus
dimethylsulfoxyde
ChemIDplus
dimetil sulfoxido
ChemIDplus
dmso
IUPAC
methylsulfinylmethane
ChemIDplus
sulfinylbis(methane)
ChemIDplus
An alpha-amino acid that consists of butyric acid bearing an amino substituent at position 2 and a carbamoyl substituent at position 4.
Glutamine
glutamine
2,5-diamino-5-oxopentanoic acid
2-Aminoglutaramic acid
2-amino-4-carbamoylbutanoic acid
Glutamin
Glutaminsaeure-5-amid
Hgln
glutamic acid gamma-amide
glutamine
Glutamine
KEGG_COMPOUND
glutamine
IUPAC
2,5-diamino-5-oxopentanoic acid
IUPAC
2-Aminoglutaramic acid
KEGG_COMPOUND
2-amino-4-carbamoylbutanoic acid
JCBN
Glutamin
ChEBI
Glutaminsaeure-5-amid
ChEBI
Hgln
IUPAC
glutamic acid gamma-amide
ChEBI
A cyclic carotene with a beta- and an epsilon-ring at opposite ends respectively.
alpha-Carotene
alpha-carotene
beta,epsilon-carotene
all-trans-alpha-carotene
alpha-carotene
alpha-Carotene
KEGG_COMPOUND
alpha-carotene
UniProt
beta,epsilon-carotene
IUPAC
all-trans-alpha-carotene
ChemIDplus
A bromoalkane that is ethane carrying bromo substituents at positions 1 and 2. It is produced by marine algae.
1,2-Dibromoethane
1,2-dibromoethane
DBE
EDB
Ethylene dibromide
alpha,beta-dibromoethane
alpha,omega-dibromoethane
ethylene bromide
sym-Dibromoethane
1,2-dibromoethane
1,2-Dibromoethane
KEGG_COMPOUND
1,2-dibromoethane
IUPAC
1,2-dibromoethane
UniProt
DBE
NIST_Chemistry_WebBook
EDB
NIST_Chemistry_WebBook
Ethylene dibromide
KEGG_COMPOUND
alpha,beta-dibromoethane
NIST_Chemistry_WebBook
alpha,omega-dibromoethane
ChemIDplus
ethylene bromide
NIST_Chemistry_WebBook
sym-Dibromoethane
ChemIDplus
A one-carbon compound that is ammonia in which one of the hydrogens is replaced by a carboxy group. Although carbamic acid derivatives are common, carbamic acid itself has never been synthesised.
CARBAMIC ACID
Carbamic acid
carbamic acid
Aminoameisensaeure
Aminoformic acid
Carbamate
Carbamidsaeure
carbamic acid
CARBAMIC ACID
PDBeChem
Carbamic acid
KEGG_COMPOUND
carbamic acid
IUPAC
Aminoameisensaeure
ChEBI
Aminoformic acid
KEGG_COMPOUND
Carbamate
KEGG_COMPOUND
Carbamidsaeure
ChEBI
phosphorus
15P
P
Phosphor
Phosphorus
fosforo
phosphore
phosphorus
phosphorus atom
phosphorus
IUPAC
15P
IUPAC
P
IUPAC
P
KEGG_COMPOUND
Phosphor
ChEBI
Phosphorus
KEGG_COMPOUND
fosforo
ChEBI
phosphore
ChEBI
phosphorus
ChEBI
molybdenum
42Mo
Mo
Molybdaen
Molybdenum
molibdeno
molybdene
molybdenum
molybdenum atom
molybdenum
IUPAC
42Mo
IUPAC
Mo
IUPAC
Mo
UniProt
Molybdaen
ChEBI
Molybdenum
KEGG_COMPOUND
molibdeno
ChEBI
molybdene
ChEBI
molybdenum
ChEBI
copper
29Cu
Copper
Cu
Kupfer
cobre
copper
cuivre
cuprum
copper atom
copper
IUPAC
29Cu
IUPAC
Copper
KEGG_COMPOUND
Cu
ChEBI
Cu
IUPAC
Kupfer
ChEBI
cobre
ChEBI
copper
ChEBI
cuivre
ChEBI
cuprum
IUPAC
A metal fluoride salt with a Na(+) counterion.
Sodium fluoride
sodium fluoride
NaF
sodium fluoride
Sodium fluoride
KEGG_COMPOUND
sodium fluoride
IUPAC
NaF
IUPAC
A ketohexose that is an isomer of glucose.
Fructose
arabino-hex-2-ulose
fructose
Fru
Fruchtzucker
Fruktose
arabino-Hexulose
fructose
Fructose
KEGG_COMPOUND
arabino-hex-2-ulose
IUPAC
fructose
IUPAC
Fru
JCBN
Fruchtzucker
ChEBI
Fruktose
ChEBI
arabino-Hexulose
KEGG_COMPOUND
beta-D-Glucan
beta-D-glucans
beta-Glucan
beta-D-glucan
beta-D-Glucan
KEGG_COMPOUND
beta-D-glucans
ChEBI
beta-Glucan
KEGG_COMPOUND
A monocarboxylic acid that is butanoic acid substituted at position 4 by a 4-[bis(2-chloroethyl)amino]phenyl group. A chemotherapy drug that can be used in combination with the antibody obinutuzumab for the treatment of chronic lymphocytic leukemia.
4-{4-[bis(2-chloroethyl)amino]phenyl}butanoic acid
CHLORAMBUCIL
Chlorambucil
4-(p-bis(beta-chloroethyl)aminophenyl)butyric acid
4-[p-[bis(2-chloroethyl)amino]phenyl]butyric acid
Ambochlorin
Leukeran
N,N-di-2-chloroethyl-gamma-p-aminophenylbutyric acid
chloraminophen
gamma-[p-di(2-chloroethyl)aminophenyl]butyric acid
phenylbutyric acid nitrogen mustard
chlorambucil
4-{4-[bis(2-chloroethyl)amino]phenyl}butanoic acid
IUPAC
CHLORAMBUCIL
PDBeChem
Chlorambucil
KEGG_DRUG
4-(p-bis(beta-chloroethyl)aminophenyl)butyric acid
NIST_Chemistry_WebBook
4-[p-[bis(2-chloroethyl)amino]phenyl]butyric acid
NIST_Chemistry_WebBook
Ambochlorin
NIST_Chemistry_WebBook
Leukeran
NIST_Chemistry_WebBook
N,N-di-2-chloroethyl-gamma-p-aminophenylbutyric acid
NIST_Chemistry_WebBook
chloraminophen
ChemIDplus
gamma-[p-di(2-chloroethyl)aminophenyl]butyric acid
NIST_Chemistry_WebBook
phenylbutyric acid nitrogen mustard
ChemIDplus
A C19-gibberellin that is a pentacyclic diterpenoid responsible for promoting growth and elongation of cells in plants. Initially identified in Gibberella fujikuroi,it differs from gibberellin A1 in the presence of a double bond between C-3 and C-4.
(1R,2R,5S,8S,9S,10R,11S,12S)-5,12-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1(5,8).0(1,10).0(2,8)]heptadec-13-ene-9-carboxylic acid
2beta,7alpha-dihydroxy-1beta-methyl-8-methylidene-13-oxo-4a,1alpha-epoxymethano-4aalpha,4bbeta-gibb-3-ene-10beta-carboxylic acid
Gibberellin A3
(+)-gibberellic acid
GA3
Gibberellin
Gibberellinsaeure
gibberellic acid
gibberellic acid GA3
gibberellin 3
gibberellin A3
(1R,2R,5S,8S,9S,10R,11S,12S)-5,12-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1(5,8).0(1,10).0(2,8)]heptadec-13-ene-9-carboxylic acid
IUPAC
2beta,7alpha-dihydroxy-1beta-methyl-8-methylidene-13-oxo-4a,1alpha-epoxymethano-4aalpha,4bbeta-gibb-3-ene-10beta-carboxylic acid
IUPAC
Gibberellin A3
KEGG_COMPOUND
(+)-gibberellic acid
ChEBI
GA3
ChEBI
Gibberellin
KEGG_COMPOUND
Gibberellinsaeure
ChEBI
gibberellic acid
ChemIDplus
gibberellic acid GA3
ChemIDplus
gibberellin 3
ChEBI
(3R,3'R,6'R)-beta,epsilon-carotene-3,3'-diol
Lutein
lutein
(3R,3'R,6S)-4,5-DIDEHYDRO-5,6-DIHYDRO-BETA,BETA-CAROTENE-3,3'-DIOL
Bo-Xan
E 161b
Xanthophyll
lutein
(3R,3'R,6'R)-beta,epsilon-carotene-3,3'-diol
IUPAC
Lutein
KEGG_COMPOUND
lutein
UniProt
(3R,3'R,6S)-4,5-DIDEHYDRO-5,6-DIHYDRO-BETA,BETA-CAROTENE-3,3'-DIOL
PDBeChem
Bo-Xan
ChemIDplus
E 161b
ChEBI
Xanthophyll
KEGG_COMPOUND
A C18 straight-chain saturated fatty acid component of many animal and vegetable lipids. As well as in the diet, it is used in hardening soaps, softening plastics and in making cosmetics, candles and plastics.
Octadecanoic acid
octadecanoic acid
18:0
C18:0
CH3-[CH2]16-COOH
Octadecansaeure
Oktadekansaeure
STEARIC ACID
Stearinsaeure
acide octadecanoique
acide stearique
n-octadecanoic acid
octadecoic acid
stearic acid
octadecanoic acid
Octadecanoic acid
KEGG_COMPOUND
octadecanoic acid
IUPAC
18:0
ChEBI
C18:0
ChemIDplus
CH3-[CH2]16-COOH
IUPAC
Octadecansaeure
ChemIDplus
Oktadekansaeure
ChEBI
STEARIC ACID
PDBeChem
Stearinsaeure
ChemIDplus
acide octadecanoique
ChEBI
acide stearique
ChEBI
n-octadecanoic acid
NIST_Chemistry_WebBook
octadecoic acid
ChEBI
stearic acid
ChEBI
A chlorophenoxyacetic acid that is phenoxyacetic acid in which the ring hydrogens at postions 2 and 4 are substituted by chlorines.
(2,4-dichlorophenoxy)acetic acid
2,4-D
(2,4-Dichlorphenoxy)essigsaeure
2,4-D acid
2,4-Dichlorophenoxyacetate
2,4-Dichlorophenoxyacetic acid
2,4-Dichlorphenoxyessigsaeure
Hedonal
Trinoxol
acide 2,4-dichloro phenoxyacetique
2,4-D
(2,4-dichlorophenoxy)acetic acid
IUPAC
2,4-D
KEGG_COMPOUND
(2,4-Dichlorphenoxy)essigsaeure
ChEBI
2,4-D acid
ChemIDplus
2,4-Dichlorophenoxyacetate
KEGG_COMPOUND
2,4-Dichlorophenoxyacetic acid
KEGG_COMPOUND
2,4-Dichlorphenoxyessigsaeure
ChEBI
Hedonal
NIST_Chemistry_WebBook
Trinoxol
NIST_Chemistry_WebBook
acide 2,4-dichloro phenoxyacetique
ChemIDplus
The conjugate base of a fatty acid, arising from deprotonation of the carboxylic acid group of the corresponding fatty acid.
Fatty acid anion
Alkanate
Fettsaeureanion
Fettsaeureanionen
a fatty acid
acido graso anionico
acidos grasos anionicos
anion de l'acide gras
fatty acid anions
fatty acid anion
Fatty acid anion
KEGG_COMPOUND
Alkanate
KEGG_COMPOUND
Fettsaeureanion
ChEBI
Fettsaeureanionen
ChEBI
a fatty acid
UniProt
acido graso anionico
ChEBI
acidos grasos anionicos
ChEBI
anion de l'acide gras
ChEBI
fatty acid anions
ChEBI
A phenylalanine derivative comprising L-phenylalanine having [bis(2-chloroethyl)amino group at the 4-position on the phenyl ring.
4-[bis(2-chloroethyl)amino]-L-phenylalanine
3-(p-(Bis(2-chloroethyl)amino)phenyl)-L-alanine
3-p-(Di(2-chloroethyl)amino)-phenyl-L-alanine
4-(Bis(2-chloroethyl)amino)-L-phenylalanine
L-3-(p-(Bis(2-chloroethyl)amino)phenyl)alanine
L-PAM
L-Phenylalanine mustard
L-Sarcolysine
Phenylalanine mustard
Phenylalanine nitrogen mustard
melfalano
melphalan
melphalanum
p-Bis(beta-chloroethyl)aminophenylalanine
p-Di-(2-chloroethyl)amino-L-phenylalanine
p-L-Sarcolysin
p-N,N-bis(2-chloroethyl)amino-L-phenylalanine
p-N-Bis(2-chloroethyl)amino-L-phenylalanine
melphalan
4-[bis(2-chloroethyl)amino]-L-phenylalanine
IUPAC
3-(p-(Bis(2-chloroethyl)amino)phenyl)-L-alanine
ChemIDplus
3-p-(Di(2-chloroethyl)amino)-phenyl-L-alanine
ChemIDplus
4-(Bis(2-chloroethyl)amino)-L-phenylalanine
ChemIDplus
L-3-(p-(Bis(2-chloroethyl)amino)phenyl)alanine
ChemIDplus
L-PAM
ChemIDplus
L-Phenylalanine mustard
ChemIDplus
L-Sarcolysine
ChemIDplus
Phenylalanine mustard
ChemIDplus
Phenylalanine nitrogen mustard
ChemIDplus
melfalano
ChemIDplus
melphalan
KEGG_DRUG
melphalanum
ChemIDplus
p-Bis(beta-chloroethyl)aminophenylalanine
ChemIDplus
p-Di-(2-chloroethyl)amino-L-phenylalanine
ChemIDplus
p-L-Sarcolysin
ChemIDplus
p-N,N-bis(2-chloroethyl)amino-L-phenylalanine
ChEBI
p-N-Bis(2-chloroethyl)amino-L-phenylalanine
ChemIDplus
A methanesulfonate ester that is butane-1,4-diol in which the hydrogens of the hydroxy groups are replaced by methanesulfonyl groups. An alkylating antineoplastic agent, it is used for the treatment of chronic myeloid leukemia (although it has been largely replaced by newer drugs). It is also used as an insect sterilant.
Busulfan
butane-1,4-diyl dimethanesulfonate
1,4-Bis(methanesulfonoxy)butane
1,4-Butanediol dimethanesulfonate
1,4-Dimesyloxybutane
1,4-Dimethanesulfonoxybutane
Bisulfex
Leucosulfan
Mablin
Mielucin
Misulban
Mitostan
Myeloleukon
Myleran
Tetramethylene bis(methanesulfonate)
busulfan
busulfano
busulfanum
busulfan
Busulfan
KEGG_DRUG
butane-1,4-diyl dimethanesulfonate
IUPAC
1,4-Bis(methanesulfonoxy)butane
ChemIDplus
1,4-Butanediol dimethanesulfonate
ChemIDplus
1,4-Dimesyloxybutane
ChemIDplus
1,4-Dimethanesulfonoxybutane
ChemIDplus
Bisulfex
ChEBI
Leucosulfan
ChEBI
Mablin
ChEBI
Mielucin
ChEBI
Misulban
ChEBI
Mitostan
ChEBI
Myeloleukon
ChEBI
Myleran
KEGG_DRUG
Tetramethylene bis(methanesulfonate)
ChemIDplus
busulfan
WHO_MedNet
busulfano
WHO_MedNet
busulfanum
WHO_MedNet
An onium cation obtained by protonation of ammonia.
ammonium
azanium
Ammonium(1+)
NH4(+)
NH4+
[NH4](+)
ammonium cation
ammonium ion
ammonium
ammonium
ChEBI
ammonium
IUPAC
azanium
IUPAC
Ammonium(1+)
ChemIDplus
NH4(+)
IUPAC
NH4(+)
UniProt
NH4+
KEGG_COMPOUND
[NH4](+)
MolBase
ammonium cation
ChemIDplus
ammonium ion
PDBeChem
2-hydroxy-3,8,9-trimethoxy-5-methylbenzo[c]phenanthridinium
Fagaronine
fagaronine
2-hydroxy-3,8,9-trimethoxy-5-methylbenzo[c]phenanthridinium
IUPAC
Fagaronine
KEGG_COMPOUND
Any sugar having one or more alcoholic hydroxy groups replaced by substituted or unsubstituted amino groups.
Aminosugars
amino sugars
aminosugar
amino sugar
Aminosugars
KEGG_COMPOUND
amino sugars
ChEBI
aminosugar
ChEBI
A carboxylic acid dianion obtained by deprotonation of both carboxy groups of any dicarboxylic acid.
dicarboxylic acid dianion
a dicarboxylate
dicarboxylate
dicarboxylates
dicarboxylic acid dianions
dicarboxylic acid dianion
dicarboxylic acid dianion
ChEBI
a dicarboxylate
UniProt
dicarboxylate
ChEBI
dicarboxylates
ChEBI
dicarboxylic acid dianions
ChEBI
A family of magnesium porphyrins, defined by the presence of a fifth ring beyond the four pyrrole-like rings. The rings can have various side chains which usually include a long phytol chain.
Chlorophyll
chlorophyll
chlorophylls
chlorophyll
Chlorophyll
KEGG_COMPOUND
chlorophyll
JCBN
chlorophylls
IUPAC
Carbonic acid
carbonic acid
dihydroxidooxidocarbon
Dihydrogen carbonate
H2CO3
Koehlensaeure
[CO(OH)2]
carbonic acid
Carbonic acid
KEGG_COMPOUND
carbonic acid
IUPAC
dihydroxidooxidocarbon
IUPAC
Dihydrogen carbonate
KEGG_COMPOUND
H2CO3
IUPAC
H2CO3
KEGG_COMPOUND
Koehlensaeure
ChEBI
[CO(OH)2]
IUPAC
aluminium
13Al
Al
Aluminium
aluminio
aluminium
aluminum
aluminium atom
aluminium
IUPAC
13Al
IUPAC
Al
IUPAC
Al
KEGG_COMPOUND
Aluminium
ChEBI
Aluminium
KEGG_COMPOUND
aluminio
ChEBI
aluminium
ChEBI
aluminum
NIST_Chemistry_WebBook
An alpha-amino acid that is glycine in which the alpha-is substituted by a 3-guanidinopropyl group.
Arginine
arginine
2-Amino-5-guanidinovaleric acid
2-amino-5-(carbamimidamido)pentanoic acid
2-amino-5-guanidinopentanoic acid
Arginin
Harg
arginine
Arginine
KEGG_COMPOUND
arginine
IUPAC
2-Amino-5-guanidinovaleric acid
KEGG_COMPOUND
2-amino-5-(carbamimidamido)pentanoic acid
IUPAC
2-amino-5-guanidinopentanoic acid
JCBN
Arginin
ChEBI
Harg
IUPAC
A member of the class of 6-aminopurines that is adenine in which one of the hydrogens of the amino group is replaced by a benzyl group.
N-Benzyladenine
N-benzyl-9H-purin-6-amine
6-(benzylamino)purine
6-BAP
6-Benzylaminopurine
6-[(phenylmethyl)amino]-9H-purine
BAP
Cytokinin B
N(6)-(benzylamino)purine
N-BENZYL-9H-PURIN-6-AMINE
N6-Benzyladenine
benzyladenine
N-benzyladenine
N-Benzyladenine
KEGG_COMPOUND
N-benzyl-9H-purin-6-amine
IUPAC
6-(benzylamino)purine
NIST_Chemistry_WebBook
6-BAP
ChemIDplus
6-Benzylaminopurine
KEGG_COMPOUND
6-[(phenylmethyl)amino]-9H-purine
NIST_Chemistry_WebBook
BAP
ChemIDplus
Cytokinin B
ChemIDplus
N(6)-(benzylamino)purine
ChemIDplus
N-BENZYL-9H-PURIN-6-AMINE
PDBeChem
N6-Benzyladenine
KEGG_COMPOUND
benzyladenine
ChemIDplus
Iron(2+)
iron(2+)
iron(2+) ion
iron(II) cation
FE (II) ION
Fe(2+)
Fe(II)
Fe2+
Ferrous ion
iron ion(2+)
iron(2+)
Iron(2+)
KEGG_COMPOUND
iron(2+)
IUPAC
iron(2+) ion
IUPAC
iron(II) cation
IUPAC
FE (II) ION
PDBeChem
Fe(2+)
UniProt
Fe(II)
KEGG_COMPOUND
Fe2+
KEGG_COMPOUND
Ferrous ion
KEGG_COMPOUND
iron ion(2+)
ChemIDplus
A divalent metal cation in which the metal is manganese.
manganese(2+)
manganese(2+) ion
manganese(II) cation
MANGANESE (II) ION
Mn(2+)
Mn(II)
Mn2+
manganese(II)
manganese, ion (Mn2+)
manganous ion
manganese(2+)
manganese(2+)
IUPAC
manganese(2+) ion
IUPAC
manganese(II) cation
IUPAC
MANGANESE (II) ION
PDBeChem
Mn(2+)
ChEBI
Mn(2+)
UniProt
Mn(II)
ChEBI
Mn2+
ChEBI
manganese(II)
ChemIDplus
manganese, ion (Mn2+)
ChemIDplus
manganous ion
ChemIDplus
An ion of copper carrying a double positive charge.
copper(2+)
copper(2+) ion
copper(II) cation
COPPER (II) ION
Cu(2+)
Cu(II)
Cu2+
copper(II) cation
copper, ion (Cu2+)
cupric ion
copper(2+)
copper(2+)
IUPAC
copper(2+) ion
IUPAC
copper(II) cation
IUPAC
COPPER (II) ION
PDBeChem
Cu(2+)
UniProt
Cu(II)
ChEBI
Cu2+
ChEBI
copper(II) cation
ChEBI
copper, ion (Cu2+)
ChemIDplus
cupric ion
ChEBI
The conjugate base formed when the carboxy group of a carboxylic acid is deprotonated.
a carboxylate
carboxylic acid anions
carboxylic anions
carboxylic acid anion
a carboxylate
UniProt
carboxylic acid anions
ChEBI
carboxylic anions
ChEBI
A monoatomic monocation obtained from sodium.
sodium cation
sodium(1+)
sodium(1+) ion
sodium(I) cation
Na(+)
Na+
SODIUM ION
sodium(1+)
sodium cation
IUPAC
sodium(1+)
IUPAC
sodium(1+) ion
IUPAC
sodium(I) cation
IUPAC
Na(+)
IUPAC
Na(+)
UniProt
Na+
KEGG_COMPOUND
SODIUM ION
PDBeChem
A monoatomic monocation obtained from potassium.
potassium cation
potassium(1+)
potassium(1+) ion
potassium(I) cation
K(+)
K+
POTASSIUM ION
potassium(1+)
potassium cation
IUPAC
potassium(1+)
IUPAC
potassium(1+) ion
IUPAC
potassium(I) cation
IUPAC
K(+)
IUPAC
K(+)
UniProt
K+
KEGG_COMPOUND
POTASSIUM ION
PDBeChem
zinc(2+)
zinc(2+) ion
zinc(II) cation
ZINC ION
Zn(2+)
Zn(II)
Zn2+
dietary zinc
zinc cation
zinc, ion (Zn2+)
zinc(2+)
zinc(2+)
IUPAC
zinc(2+) ion
IUPAC
zinc(II) cation
IUPAC
ZINC ION
PDBeChem
Zn(2+)
IUPAC
Zn(2+)
UniProt
Zn(II)
KEGG_COMPOUND
Zn2+
KEGG_COMPOUND
dietary zinc
ChEBI
zinc cation
IUPAC
zinc, ion (Zn2+)
ChemIDplus
calcium(2+)
calcium(2+) ion
calcium(II) cation
CALCIUM ION
Ca(2+)
Ca2+
calcium, doubly charged positive ion
calcium(2+)
calcium(2+)
IUPAC
calcium(2+) ion
IUPAC
calcium(II) cation
IUPAC
CALCIUM ION
PDBeChem
Ca(2+)
IUPAC
Ca(2+)
UniProt
Ca2+
KEGG_COMPOUND
calcium, doubly charged positive ion
NIST_Chemistry_WebBook
dioxidanide
hydrogen(peroxide)(1-)
hydrogendioxide(1-)
hydrogenperoxide(1-)
HO2(-)
HOO anion
HOO(-)
[HO2](-)
hydrogenperoxide(1-)
dioxidanide
IUPAC
hydrogen(peroxide)(1-)
IUPAC
hydrogendioxide(1-)
IUPAC
hydrogenperoxide(1-)
IUPAC
HO2(-)
IUPAC
HOO anion
NIST_Chemistry_WebBook
HOO(-)
ChEBI
[HO2](-)
ChEBI
hydridohydroxidodioxidosulfur
sulfonic acid
HSHO3
Sulfonsaeure
[SHO2(OH)]
acide sulfonique
sulphonic acid
sulfonic acid
hydridohydroxidodioxidosulfur
IUPAC
sulfonic acid
IUPAC
HSHO3
IUPAC
Sulfonsaeure
ChEBI
[SHO2(OH)]
IUPAC
acide sulfonique
ChEBI
sulphonic acid
ChEBI
A diatomic molecule containing covalently bonded hydrogen and fluorine atoms.
Hydrogen fluoride
fluorane
fluoridohydrogen
hydrogen fluoride
Fluoride
Fluorwasserstoff
HF
Hydrogenfluorid
[HF]
fluorure d'hydrogene
hydrofluoric acid
hydrogen fluoride
Hydrogen fluoride
KEGG_COMPOUND
fluorane
IUPAC
fluoridohydrogen
IUPAC
hydrogen fluoride
IUPAC
Fluoride
KEGG_COMPOUND
Fluorwasserstoff
ChEBI
HF
IUPAC
Hydrogenfluorid
ChEBI
[HF]
IUPAC
fluorure d'hydrogene
ChEBI
hydrofluoric acid
ChemIDplus
Nucleus of the (3)H atom.
tritium(1+)
triton
(3)1H(+)
(3)H(+)
T(+)
t
t(+)
triton
tritium(1+)
IUPAC
triton
IUPAC
(3)1H(+)
IUPAC
(3)H(+)
IUPAC
T(+)
IUPAC
t
IUPAC
t(+)
IUPAC
The radioactive isotope of hydrogen with relative atomic mass 3.016049 and half-life of 12.33 years (from Greek taurhoiotatauomicronsigma, third).
tritium
(3)1H
(3)H
T
hydrogen-3
tritio
tritium
ueberschwerer Wasserstoff
tritium atom
tritium
IUPAC
(3)1H
IUPAC
(3)H
IUPAC
T
IUPAC
hydrogen-3
ChEBI
tritio
ChEBI
tritium
ChEBI
ueberschwerer Wasserstoff
ChEBI
dihydrogen(trioxidoborate)(1-)
dihydrogenborate
dihydroxidooxidoborate(1-)
H2BO3(-)
[BO(OH)2](-)
dihydrogenborate
dihydrogen(trioxidoborate)(1-)
IUPAC
dihydrogenborate
IUPAC
dihydroxidooxidoborate(1-)
IUPAC
H2BO3(-)
IUPAC
[BO(OH)2](-)
IUPAC
hydrogen(trioxidoborate)(2-)
hydrogenborate
hydroxidodioxidoborate(2-)
HBO3(2-)
[BO2(OH)](2-)
hydrogenborate
hydrogen(trioxidoborate)(2-)
IUPAC
hydrogenborate
IUPAC
hydroxidodioxidoborate(2-)
IUPAC
HBO3(2-)
IUPAC
[BO2(OH)](2-)
IUPAC
A monovalent inorganic anion obtained by deprotonation of phosphorous acid.
dihydrogen(trioxidophosphate)(1-)
dihydrogenphosphite
dihydroxidooxidophosphate(1-)
H2PO3(-)
[PO(OH)2] (-)
dihydrogen phosphite
dihydrogenphosphite
dihydrogen(trioxidophosphate)(1-)
IUPAC
dihydrogenphosphite
IUPAC
dihydroxidooxidophosphate(1-)
IUPAC
H2PO3(-)
IUPAC
[PO(OH)2] (-)
IUPAC
dihydrogen phosphite
ChEBI
A divalent inorganic anion resulting from the removal of a proton from two of the hydroxy groups of phosphorous acid.
hydrogen(trioxidophosphate)(2-)
hydrogenphosphite
hydroxidodioxidophosphate(2-)
HPO3(2-)
[PO2(OH)](2-)
hydrogen phosphite
hydrogenphosphite
hydrogen(trioxidophosphate)(2-)
IUPAC
hydrogenphosphite
IUPAC
hydroxidodioxidophosphate(2-)
IUPAC
HPO3(2-)
IUPAC
[PO2(OH)](2-)
IUPAC
hydrogen phosphite
IUPAC
alkyl sulfates
alkyl sulfate
alkyl sulfates
ChEBI
amide
azanide
dihydridonitrate(1-)
NH2(-)
azanide
amide
IUPAC
azanide
IUPAC
dihydridonitrate(1-)
IUPAC
NH2(-)
IUPAC
A divalent inorganic anion resulting from the removal of two protons from ammonia.
azanediide
hydridonitrate(2-)
NH(2-)
imide
hydridonitrate(2-)
azanediide
IUPAC
hydridonitrate(2-)
IUPAC
NH(2-)
IUPAC
imide
IUPAC
A carboxamide derived from a monocarboxylic acid.
monocarboxylic acid amides
monocarboxylic acid amide
monocarboxylic acid amides
ChEBI
ethane-1,2-diyl
ethylene
-CH2-CH2-
ethano
ethylene group
ethane-1,2-diyl
IUPAC
ethylene
IUPAC
-CH2-CH2-
IUPAC
ethano
IUPAC
peroxy
-OO-
peroxy group
peroxy
IUPAC
-OO-
IUPAC
aquahydrogen(1+)
oxidanium
oxonium
trihydridooxygen(1+)
H3O(+)
Hydronium cation
Hydronium ion
[OH3](+)
oxonium
aquahydrogen(1+)
IUPAC
oxidanium
IUPAC
oxonium
IUPAC
trihydridooxygen(1+)
IUPAC
H3O(+)
IUPAC
Hydronium cation
NIST_Chemistry_WebBook
Hydronium ion
ChemIDplus
[OH3](+)
MolBase
A monocarboxylic acid anion obtained by the deprotonation of the carboxy group of ferulic acid.
(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate
(E)-ferulate
3-methoxy-4-hydroxy-trans-cinnamate
ferulate
(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate
IUPAC
(E)-ferulate
UniProt
3-methoxy-4-hydroxy-trans-cinnamate
ChEBI
nitro
-NO2
nitro group
nitro
IUPAC
-NO2
IUPAC
dioxidanyl
hydroperoxy
-OOH
hydroperoxy group
dioxidanyl
IUPAC
hydroperoxy
IUPAC
-OOH
IUPAC
A hydroxy monocarboxylic acid anion that is acetate where the methyl group has been hydroxylated.
glycolate
hydroxyacetate
glycolate
glycolate
UniProt
hydroxyacetate
IUPAC
A hexitol produced by a variety of organisms including bacteria, fungi, lichens and plants.
mannitol
mannitol
mannitol
IUPAC
SULFO GROUP
hydroxydioxo-lambda(6)-sulfanyl
hydroxysulfonyl
sulfo
-S(O)2(OH)
sulfo group
SULFO GROUP
PDBeChem
hydroxydioxo-lambda(6)-sulfanyl
IUPAC
hydroxysulfonyl
IUPAC
sulfo
IUPAC
-S(O)2(OH)
IUPAC
An alpha-amino-acid anion that is the conjugate base of L-glutamic acid, having anionic carboxy groups and a cationic amino group
L-glutamate(1-)
hydrogen L-glutamate
(2S)-2-ammoniopentanedioate
L-glutamate
L-glutamic acid monoanion
L-glutamic acid, ion(1-)
L-glutamate(1-)
L-glutamate(1-)
JCBN
hydrogen L-glutamate
IUPAC
(2S)-2-ammoniopentanedioate
IUPAC
L-glutamate
ChEBI
L-glutamate
UniProt
L-glutamic acid monoanion
JCBN
L-glutamic acid, ion(1-)
ChemIDplus
An alpha-amino-acid anion that is the conjugate base of D-glutamic acid, having anionic carboxy groups and a cationic amino group
D-glutamate(1-)
hydrogen D-glutamate
(2R)-2-ammoniopentanedioate
D-glutamate
D-glutamic acid monoanion
D-glutamate(1-)
D-glutamate(1-)
JCBN
hydrogen D-glutamate
IUPAC
(2R)-2-ammoniopentanedioate
IUPAC
D-glutamate
UniProt
D-glutamic acid monoanion
JCBN
A dicarboxylic acid dianion that is the conjugate base of glutamate(1-).
2-aminopentanedioate
glutamate
glutamate(2-)
glutamic acid dianion
glutamate(2-)
2-aminopentanedioate
IUPAC
glutamate
IUPAC
glutamate(2-)
JCBN
glutamic acid dianion
JCBN
An L-alpha-amino acid anion that is the dianion obtained by the deprotonation of the both the carboxy groups of L-glutamic acid.
(2S)-2-aminopentanedioate
L-glutamate
L-glutamate(2-)
L-glutamic acid dianion
L-glutamate(2-)
(2S)-2-aminopentanedioate
IUPAC
L-glutamate
IUPAC
L-glutamate(2-)
JCBN
L-glutamic acid dianion
JCBN
(2R)-2-aminopentanedioate
D-glutamate
D-glutamate(2-)
D-glutamic acid dianion
D-glutamate(2-)
(2R)-2-aminopentanedioate
IUPAC
D-glutamate
IUPAC
D-glutamate(2-)
JCBN
D-glutamic acid dianion
JCBN
An aspartate(1-) that is the conjugate base of D-aspartic acid.
D-aspartate(1-)
hydrogen D-aspartate
(2R)-2-ammoniobutanedioate
(2R)-2-ammoniosuccinate
D-aspartate
D-aspartic acid monoanion
D-aspartate(1-)
D-aspartate(1-)
JCBN
hydrogen D-aspartate
IUPAC
(2R)-2-ammoniobutanedioate
IUPAC
(2R)-2-ammoniosuccinate
ChEBI
D-aspartate
UniProt
D-aspartic acid monoanion
JCBN
An aspartate(1-) that is the conjugate base of L-aspartic acid.
L-aspartate(1-)
hydrogen L-aspartate
(2S)-2-ammoniobutanedioate
(2S)-2-ammoniosuccinate
L-aspartate
L-aspartic acid monoanion
L-aspartate(1-)
L-aspartate(1-)
JCBN
hydrogen L-aspartate
IUPAC
(2S)-2-ammoniobutanedioate
IUPAC
(2S)-2-ammoniosuccinate
ChEBI
L-aspartate
ChEBI
L-aspartate
UniProt
L-aspartic acid monoanion
JCBN
An aspartate(2-) that is the conjugate base of L-aspartate(1-).
(2S)-2-aminobutanedioate
L-aspartate
L-aspartate(2-)
(2S)-2-aminosuccinate
L-aspartic acid dianion
L-aspartate(2-)
(2S)-2-aminobutanedioate
IUPAC
L-aspartate
IUPAC
L-aspartate(2-)
JCBN
(2S)-2-aminosuccinate
ChEBI
L-aspartic acid dianion
JCBN
An aspartate(2-) that is the conjugate base of D-aspartate(1-).
(2R)-2-aminobutanedioate
D-aspartate
D-aspartate(2-)
(2R)-2-aminosuccinate
D-aspartic acid dianion
D-aspartate(2-)
(2R)-2-aminobutanedioate
IUPAC
D-aspartate
IUPAC
D-aspartate(2-)
JCBN
(2R)-2-aminosuccinate
ChEBI
D-aspartic acid dianion
JCBN
A C4-dicarboxylate that is the dianion obtained by the deprotonation of both the carboxy groups of aspartic acid.
2-aminobutanedioate
aspartate
aspartate(2-)
2-aminosuccinate
aspartic acid dianion
aspartate(2-)
2-aminobutanedioate
IUPAC
aspartate
IUPAC
aspartate(2-)
JCBN
2-aminosuccinate
ChEBI
aspartic acid dianion
JCBN
guanidinium
[C(NH2)3](+)
diaminomethaniminium
guanidine
guanidinium
guanidinium
IUPAC
[C(NH2)3](+)
ChEBI
diaminomethaniminium
IUPAC
guanidine
UniProt
A monocarboxylic acid anion resulting from the removal of a proton from the carboxy group of acetic acid.
acetate
ACETATE ION
Azetat
CH3-COO(-)
Ethanoat
MeCO2 anion
acetic acid, ion(1-)
ethanoate
acetate
acetate
IUPAC
acetate
UniProt
ACETATE ION
PDBeChem
Azetat
ChEBI
CH3-COO(-)
IUPAC
Ethanoat
ChEBI
MeCO2 anion
NIST_Chemistry_WebBook
acetic acid, ion(1-)
ChemIDplus
ethanoate
ChEBI
lithium
3Li
Li
Lithium
lithium
litio
lithium atom
lithium
IUPAC
3Li
IUPAC
Li
IUPAC
Lithium
ChEBI
lithium
ChEBI
litio
ChEBI
Particle of zero charge, zero rest mass, spin quantum number 1, energy hnu and momentum hnu/c (h is the Planck constant, nu the frequency of radiation and c the speed of light), carrier of electromagnetic force.
photon
Lichtquant
Light
foton
gamma
hnu
light quantum
photon
photon
IUPAC
Lichtquant
ChEBI
Light
KEGG_COMPOUND
foton
ChEBI
gamma
IUPAC
hnu
IUPAC
hnu
UniProt
light quantum
ChEBI
An octadecadienoate with cis- double bonds at the 9- and 12- positions; the conjugate base of linoleic acid.
(9Z,12Z)-octadeca-9,12-dienoate
(9Z,12Z)-9,12-octadecadienoic acid, ion(1-)
(9Z,12Z)-octadecadienoate
(Z,Z)-9,12-octadecadienoic acid, ion(1-)
cis,cis-9,12-octadecadienoate
cis,cis-linoleate
cis-Delta(9,12)-octadecadienoate
linoleic acid, ion(1-)
linoleate
(9Z,12Z)-octadeca-9,12-dienoate
IUPAC
(9Z,12Z)-9,12-octadecadienoic acid, ion(1-)
ChemIDplus
(9Z,12Z)-octadecadienoate
UniProt
(Z,Z)-9,12-octadecadienoic acid, ion(1-)
ChemIDplus
cis,cis-9,12-octadecadienoate
ChEBI
cis,cis-linoleate
ChEBI
cis-Delta(9,12)-octadecadienoate
ChEBI
linoleic acid, ion(1-)
ChemIDplus
benzenido
phenyl
-C6H5
C6H5-
Ph
phenyl group
benzenido
IUPAC
phenyl
IUPAC
-C6H5
ChEBI
C6H5-
IUPAC
Ph
IUPAC
Divalent cation
divalent inorganic cations
monoatomic dications
monoatomic dication
Divalent cation
KEGG_COMPOUND
divalent inorganic cations
ChEBI
monoatomic dications
ChEBI
A compound comprising a benzene ring core carrying a carboxylic acid substituent.
BENZOIC ACID
Benzoic acid
benzoic acid
Aromatic carboxylic acid
Benzenecarboxylic acid
Benzeneformic acid
Benzenemethanoic acid
Benzoesaeure
Dracylic acid
E210
Phenylcarboxylic acid
Phenylformic acid
acide benzoique
benzoic acid
BENZOIC ACID
PDBeChem
Benzoic acid
KEGG_COMPOUND
benzoic acid
IUPAC
Aromatic carboxylic acid
KEGG_COMPOUND
Benzenecarboxylic acid
KEGG_COMPOUND
Benzeneformic acid
HMDB
Benzenemethanoic acid
HMDB
Benzoesaeure
ChEBI
Dracylic acid
KEGG_COMPOUND
E210
ChEBI
Phenylcarboxylic acid
HMDB
Phenylformic acid
KEGG_COMPOUND
acide benzoique
ChEBI
The simplest carboxylic acid, containing a single carbon. Occurs naturally in various sources including the venom of bee and ant stings, and is a useful organic synthetic reagent. Principally used as a preservative and antibacterial agent in livestock feed. Induces severe metabolic acidosis and ocular injury in human subjects.
FORMIC ACID
Formic acid
formic acid
Acide formique
Ameisensaeure
H-COOH
HCO2H
HCOOH
Methanoic acid
aminic acid
bilorin
formylic acid
hydrogen carboxylic acid
methoic acid
formic acid
FORMIC ACID
PDBeChem
Formic acid
KEGG_COMPOUND
formic acid
IUPAC
Acide formique
ChemIDplus
Ameisensaeure
ChemIDplus
H-COOH
IUPAC
HCO2H
ChEBI
HCOOH
NIST_Chemistry_WebBook
Methanoic acid
KEGG_COMPOUND
aminic acid
ChemIDplus
bilorin
ChemIDplus
formylic acid
ChemIDplus
hydrogen carboxylic acid
ChemIDplus
methoic acid
ChEBI
A monohydroxybenzoate that is the conjugate base of salicylic acid.
2-hydroxybenzoate
Salicylate
salicylate
2-hydroxybenzoic acid ion(1-)
o-hydroxybenzoate
sal
salicylate
2-hydroxybenzoate
IUPAC
Salicylate
KEGG_COMPOUND
salicylate
UniProt
2-hydroxybenzoic acid ion(1-)
ChemIDplus
o-hydroxybenzoate
ChemIDplus
sal
IUPAC
A short-chain saturated fatty acid comprising ethane attached to the carbon of a carboxy group.
Propionic acid
propanoic acid
propionic acid
CH3-CH2-COOH
PA
PROPANOIC ACID
Propanoic acid
Propionsaeure
acide propanoique
acide propionique
carboxyethane
ethanecarboxylic acid
ethylformic acid
metacetonic acid
methylacetic acid
propioic acid
propoic acid
pseudoacetic acid
propionic acid
Propionic acid
KEGG_COMPOUND
propanoic acid
IUPAC
propionic acid
IUPAC
CH3-CH2-COOH
IUPAC
PA
ChEBI
PROPANOIC ACID
PDBeChem
Propanoic acid
KEGG_COMPOUND
Propionsaeure
ChEBI
acide propanoique
ChEBI
acide propionique
NIST_Chemistry_WebBook
carboxyethane
ChemIDplus
ethanecarboxylic acid
ChemIDplus
ethylformic acid
ChemIDplus
metacetonic acid
ChemIDplus
methylacetic acid
ChemIDplus
propioic acid
LIPID_MAPS
propoic acid
ChEBI
pseudoacetic acid
ChemIDplus
A C18, long straight-chain monounsaturated fatty acid anion; and the conjugate base of oleic acid, arising from deprotonation of the carboxylic acid group.
(9Z)-octadec-9-enoate
(9Z)-octadecenoate
(Z)-9-octadecenoic acid, ion(1-)
Oleat
cis-9-octadecenoate
oleic acid anion
oleate
(9Z)-octadec-9-enoate
IUPAC
(9Z)-octadecenoate
UniProt
(Z)-9-octadecenoic acid, ion(1-)
ChemIDplus
Oleat
ChEBI
cis-9-octadecenoate
CBN
oleic acid anion
ChEBI
An indol-3-yl carboxylic acid anion that is the conjugate base of indole-3-acetic acid.
1H-indol-3-ylacetate
(indol-3-yl)acetate
2-(indol-3-yl)ethanoate
indole-3-acetate
1H-indol-3-ylacetate
IUPAC
(indol-3-yl)acetate
UniProt
2-(indol-3-yl)ethanoate
ChEBI
A compound in which a hydroxy group, -OH, is attached to a saturated carbon atom.
Alcohol
alcohols
an alcohol
alcohol
Alcohol
KEGG_COMPOUND
alcohols
IUPAC
an alcohol
UniProt
Aziridine
aziridine
EI
azacyclopropane
dimethyleneimine
ethyleneimine
ethylenimine
aziridine
Aziridine
KEGG_COMPOUND
aziridine
IUPAC
EI
NIST_Chemistry_WebBook
azacyclopropane
NIST_Chemistry_WebBook
dimethyleneimine
NIST_Chemistry_WebBook
ethyleneimine
ChemIDplus
ethylenimine
NIST_Chemistry_WebBook
A short-chain fatty acid anion that is the conjugate base of valeric acid; present in ester form as component of many steroid-based pharmaceuticals.
pentanoate
CH3-[CH2]3-COO(-)
n-propylacetate
pentanoate
pentanoic acid, ion(1-)
valerate
pentanoate
IUPAC
CH3-[CH2]3-COO(-)
IUPAC
n-propylacetate
ChEBI
pentanoate
UniProt
pentanoic acid, ion(1-)
ChemIDplus
Potassium sulfate
potassium sulfate
K2SO4
Kaliumsulfat
dipotassium sulfate
potassium sulphate
potassium sulfate
Potassium sulfate
KEGG_COMPOUND
potassium sulfate
IUPAC
K2SO4
IUPAC
Kaliumsulfat
ChEBI
dipotassium sulfate
ChemIDplus
potassium sulphate
ChEBI
Sodium hydroxide
sodium hydroxide
Aetznatron
NaOH
Natriumhydroxid
caustic soda
hydroxyde de sodium
soda lye
sodium hydrate
soude caustique
sodium hydroxide
Sodium hydroxide
KEGG_COMPOUND
sodium hydroxide
IUPAC
Aetznatron
ChEBI
NaOH
IUPAC
Natriumhydroxid
NIST_Chemistry_WebBook
caustic soda
NIST_Chemistry_WebBook
hydroxyde de sodium
NIST_Chemistry_WebBook
soda lye
NIST_Chemistry_WebBook
sodium hydrate
NIST_Chemistry_WebBook
soude caustique
ChEBI
A linolenate that is the conjugate base of alpha-linolenic acid, arising from deprotonation of the carboxylic acid group.
(9Z,12Z,15Z)-octadeca-9,12,15-trienoate
(9,12,15)-linolenate
(9Z,12Z,15Z)-octadecatrienoate
all-cis--9,12,15-octadecatrienoate
cis,cis,cis-9,12,15-octadecatrienoate
linolenate
alpha-linolenate
(9Z,12Z,15Z)-octadeca-9,12,15-trienoate
IUPAC
(9,12,15)-linolenate
CBN
(9Z,12Z,15Z)-octadecatrienoate
UniProt
all-cis--9,12,15-octadecatrienoate
ChEBI
cis,cis,cis-9,12,15-octadecatrienoate
ChEBI
linolenate
ChemIDplus
An alpha-amino-acid anion that is the conjugate base of alanine, arising from deprotonation of the carboxy group.
2-aminopropanoate
alaninate
alanine anion
alaninate
2-aminopropanoate
IUPAC
alaninate
JCBN
alanine anion
JCBN
An alpha-amino-acid cation that is the conjugate acid of alanine.
1-carboxyethanaminium
alaninium
alanine cation
alaninium
1-carboxyethanaminium
IUPAC
alaninium
JCBN
alanine cation
JCBN
A sulfur-containing amino-acid anion that is the conjugate base of cysteine, obtained by deprotonation of the carboxy group.
cysteinate(1-)
hydrogen cysteinate
2-amino-3-mercaptopropanoate
2-amino-3-sulfanylpropanoate
cys(-)
cysteine monoanion
cysteinate(1-)
cysteinate(1-)
JCBN
hydrogen cysteinate
IUPAC
2-amino-3-mercaptopropanoate
ChEBI
2-amino-3-sulfanylpropanoate
IUPAC
cys(-)
IUPAC
cysteine monoanion
JCBN
cysteinate
cysteinate(2-)
2-amino-3-sulfidopropanoate
cysteine dianion
cysteinate(2-)
cysteinate
IUPAC
cysteinate(2-)
JCBN
2-amino-3-sulfidopropanoate
IUPAC
cysteine dianion
JCBN
1-carboxy-2-sulfanylethanaminium
cysteinium
1-carboxy-2-mercaptoethanaminium
H2cys(+)
cysteine cation
cysteinium
1-carboxy-2-sulfanylethanaminium
IUPAC
cysteinium
JCBN
1-carboxy-2-mercaptoethanaminium
ChEBI
H2cys(+)
IUPAC
cysteine cation
JCBN
An optically active form of phenylalaninate having L-configuration.
L-phenylalaninate
(2S)-2-amino-3-phenylpropanoate
L-phenylalanine anion
L-phenylalaninate
L-phenylalaninate
IUPAC
(2S)-2-amino-3-phenylpropanoate
IUPAC
L-phenylalanine anion
JCBN
An optically active form of phenylalaninium having L-configuration.
L-phenylalaninium
(1S)-1-carboxy-2-phenylethanaminium
L-phenylalanine cation
L-phenylalaninium
L-phenylalaninium
IUPAC
(1S)-1-carboxy-2-phenylethanaminium
IUPAC
L-phenylalanine cation
JCBN
The D-enantiomer of phenylalaninate.
D-phenylalaninate
(2R)-2-amino-3-phenylpropanoate
D-phenylalanine anion
D-phenylalaninate
D-phenylalaninate
IUPAC
(2R)-2-amino-3-phenylpropanoate
IUPAC
D-phenylalanine anion
JCBN
An optically active form of phenylalaninium having D-configuration.
D-phenylalaninium
(1R)-1-carboxy-2-phenylethanaminium
D-phenylalanine cation
D-phenylalaninium
D-phenylalaninium
IUPAC
(1R)-1-carboxy-2-phenylethanaminium
IUPAC
D-phenylalanine cation
JCBN
An aromatic amino-acid anion that is the conjugate base of phenylalanine, arising from deprotonation of the carboxy group.
phenylalaninate
2-amino-3-phenylpropanoate
phenylalanine anion
phenylalaninate
phenylalaninate
IUPAC
2-amino-3-phenylpropanoate
IUPAC
phenylalanine anion
JCBN
An alpha-amino-acid cation that is the conjugate acid of phenylalanine, arising from protonation of the amino group.
phenylalaninium
1-carboxy-2-phenylethanaminium
phenylalanine cation
phenylalaninium
phenylalaninium
IUPAC
1-carboxy-2-phenylethanaminium
IUPAC
phenylalanine cation
JCBN
An alpha-amino-acid cation that is the conjugate acid of glycine, arising from protonation of the amino.
glycinium
H2gly(+)
NH3(+)-CH2-COOH
carboxymethanaminium
glycine cation
glycinium
glycinium
IUPAC
H2gly(+)
IUPAC
NH3(+)-CH2-COOH
IUPAC
carboxymethanaminium
IUPAC
glycine cation
JCBN
An alpha-amino-acid anion that is the conjugate base of glycine, arising from deprotonation of the carboxy group.
glycinate
H2N-CH2-COO(-)
aminoacetate
gly(-)
glycine anion
glycinate
glycinate
IUPAC
H2N-CH2-COO(-)
IUPAC
aminoacetate
IUPAC
gly(-)
IUPAC
glycine anion
JCBN
A metal chloride salt with a K(+) counterion.
potassium chloride
KCl
Kaliumchlorid
Kaon-Cl 10
Klor-con
Klotrix
Monopotassium chloride
[KCl]
muriate of potash
sylvite
potassium chloride
potassium chloride
IUPAC
KCl
IUPAC
Kaliumchlorid
ChEBI
Kaon-Cl 10
KEGG_DRUG
Klor-con
KEGG_DRUG
Klotrix
KEGG_DRUG
Monopotassium chloride
DrugBank
[KCl]
MolBase
muriate of potash
NIST_Chemistry_WebBook
sylvite
ChEBI
An alpha-amino-acid anion that is the conjugate base of glutamine, arising from deprotonation of the carboxy group.
glutaminate
2,5-diamino-5-oxopentanoate
gln(-)
glutamine anion
glutaminate
glutaminate
IUPAC
2,5-diamino-5-oxopentanoate
IUPAC
gln(-)
IUPAC
glutamine anion
JCBN
An alpha-amino-acid cation that is the conjugate acid of glutamine, arising from protonation of the amino group.
glutaminium
4-amino-1-carboxy-4-oxobutan-1-aminium
H2gln(+)
glutamine cation
glutaminium
glutaminium
IUPAC
4-amino-1-carboxy-4-oxobutan-1-aminium
IUPAC
H2gln(+)
IUPAC
glutamine cation
JCBN
argininate
2-amino-5-(carbamimidamido)pentanoate
2-amino-5-guanidinopentanoate
arg(-)
arginine anion
argininate
argininate
IUPAC
2-amino-5-(carbamimidamido)pentanoate
IUPAC
2-amino-5-guanidinopentanoate
JCBN
arg(-)
IUPAC
arginine anion
JCBN
argininium
argininium(1+)
2-ammonio-5-guanidiniopentanoate
H2arg(+)
arginine
arginine monocation
argininium(1+)
argininium
IUPAC
argininium(1+)
JCBN
2-ammonio-5-guanidiniopentanoate
JCBN
H2arg(+)
IUPAC
arginine
UniProt
arginine monocation
JCBN
argininediium
argininium(2+)
(1-carboxy-4-guanidiniobutyl)ammonium
H3arg(2+)
arginine dication
argininium(2+)
argininediium
IUPAC
argininium(2+)
JCBN
(1-carboxy-4-guanidiniobutyl)ammonium
ChEBI
H3arg(2+)
IUPAC
arginine dication
JCBN
An alpha-amino-acid anion that is the conjugate base of tryptophan, arising from deprotonation of the carboxy group.
tryptophanate
2-amino-3-(1H-indol-3-yl)propanoate
trp(-)
tryptophan anion
tryptophanate
tryptophanate
IUPAC
2-amino-3-(1H-indol-3-yl)propanoate
IUPAC
trp(-)
IUPAC
tryptophan anion
JCBN
An alpha-amino-acid cation that is the conjugate acid of tryptophan, arising from protonation of the alpha-amino group.
tryptophanium
1-carboxy-2-(1H-indol-3-yl)ethanaminium
Htrp(+)
tryptophan cation
tryptophanium
tryptophanium
IUPAC
1-carboxy-2-(1H-indol-3-yl)ethanaminium
IUPAC
Htrp(+)
IUPAC
tryptophan cation
JCBN
An alpha-amino-acid anion that is the conjugate base of proline, arising from deprotonation of the carboxy group.
prolinate
pro(-)
proline anion
pyrrolidine-2-carboxylate
prolinate
prolinate
IUPAC
pro(-)
IUPAC
proline anion
JCBN
pyrrolidine-2-carboxylate
IUPAC
An alpha-amino-acid cation that is the conjugate acid of proline, arising from protonation of the amino group.
prolinium
2-carboxypyrrolidinium
H2pro(+)
proline cation
prolinium
prolinium
IUPAC
2-carboxypyrrolidinium
IUPAC
H2pro(+)
IUPAC
proline cation
JCBN
An acyclic branched or unbranched hydrocarbon having one carbon-carbon double bond and the general formula CnH2n. Acyclic branched or unbranched hydrocarbons having more than one double bond are alkadienes, alkatrienes, etc.
Alkene
alkenes
olefin
alkene
Alkene
KEGG_COMPOUND
alkenes
ChEBI
olefin
ChEBI
A naphthylacetic acid substituted by a carboxymethyl group at position 1.
1-naphthaleneacetic acid
naphthalen-1-ylacetic acid
(naphthalen-1-yl)acetic acid
1-Naphthylacetic acid
NAA
NAPHTHALEN-1-YL-ACETIC ACID
alpha-NAA
alpha-naphthaleneacetic acid
naphthalene-1-acetic acid
1-naphthaleneacetic acid
1-naphthaleneacetic acid
NIST_Chemistry_WebBook
naphthalen-1-ylacetic acid
IUPAC
(naphthalen-1-yl)acetic acid
IUPAC
1-Naphthylacetic acid
KEGG_COMPOUND
NAA
ChemIDplus
NAA
KEGG_COMPOUND
NAPHTHALEN-1-YL-ACETIC ACID
PDBeChem
alpha-NAA
NIST_Chemistry_WebBook
alpha-naphthaleneacetic acid
NIST_Chemistry_WebBook
naphthalene-1-acetic acid
NIST_Chemistry_WebBook
A straight-chain alkane carrying 18 carbon atoms.
octadecane
CH3-[CH2]16-CH3
Oktadekan
n-octadecane
octadecane
octadecane
IUPAC
CH3-[CH2]16-CH3
IUPAC
Oktadekan
ChEBI
n-octadecane
NIST_Chemistry_WebBook
Any cyclic ether in which the oxygen atom forms part of a 3-membered ring.
Epoxide
epoxides
Alkene oxide
Olefin oxide
an epoxide
epoxides
epoxide
Epoxide
KEGG_COMPOUND
epoxides
IUPAC
Alkene oxide
KEGG_COMPOUND
Olefin oxide
KEGG_COMPOUND
an epoxide
UniProt
epoxides
ChEBI
2,5-diaminopentanoate
ornithinate
ornithine anion
ornithinate
2,5-diaminopentanoate
IUPAC
ornithinate
IUPAC
ornithine anion
JCBN
An amide is a derivative of an oxoacid RkE(=O)l(OH)m (l =/= 0) in which an acidic hydroxy group has been replaced by an amino or substituted amino group.
Amide
amides
amide
Amide
KEGG_COMPOUND
amides
IUPAC
iodine(1+)
iodine cation
iodine(1+)
iodine(1+)
IUPAC
iodine cation
NIST_Chemistry_WebBook
BORIC ACID
Boric acid
boric acid
trihydroxidoboron
B(OH)3
H3BO3
[B(OH)3]
boron trihydroxide
orthoboric acid
boric acid
BORIC ACID
PDBeChem
Boric acid
KEGG_COMPOUND
boric acid
IUPAC
trihydroxidoboron
IUPAC
B(OH)3
NIST_Chemistry_WebBook
H3BO3
IUPAC
[B(OH)3]
MolBase
boron trihydroxide
NIST_Chemistry_WebBook
orthoboric acid
NIST_Chemistry_WebBook
boron oxoacid
boron oxoacids
oxoacids of boron
boron oxoacid
boron oxoacid
ChEBI
boron oxoacids
ChEBI
oxoacids of boron
ChEBI
A biochemical role played by any micronutrient that is an organic compound. Vitamins are present in foods in small amounts and are essential to normal metabolism and biochemical functions, usually as coenzymes. The term "vitamines" (from vita + amines) was coined in 1912 by Casimir Funk, who believed that these compounds were amines.
vitamin
vitamina
vitaminas
vitamine
vitamines
vitamins
vitaminum
vitamin (role)
vitamin
ChEBI
vitamina
ChEBI
vitaminas
ChEBI
vitamine
ChEBI
vitamines
ChEBI
vitamins
ChEBI
vitaminum
ChEBI
Intended use of the molecular entity or part thereof by humans.
application
A particle not known to have substructure.
elementary particle
elementary particles
fundamental particle
elementary particle
IUPAC
elementary particles
ChEBI
A monoatomic entity is a molecular entity consisting of a single atom.
atomic entity
monoatomic entities
monoatomic entity
atomic entity
ChEBI
monoatomic entities
ChEBI
An assembly consisting of a central atom (usually metallic) to which is attached a surrounding array of other groups of atoms (ligands).
coordination entities
coordination entity
coordination compounds
coordination entity
coordination entities
IUPAC
coordination entity
IUPAC
coordination compounds
ChEBI
oxoacid derivatives
oxoacid derivative
oxoacid derivatives
ChEBI
inorganic hydrides
inorganic hydride
inorganic hydrides
ChEBI
An organic fundamental parent is a structure used as a basis for substitutive names in organic nomenclature, containing, in addition to one or more hydrogen atoms, a single atom of an element, a number of atoms (alike or different) linked together to form an unbranched chain, a monocyclic or polycyclic ring system, or a ring assembly or ring/chain system.
organic fundamental parents
organic parent hydrides
organic fundamental parent
organic fundamental parents
ChEBI
organic parent hydrides
ChEBI
Any substituent group which does not contain carbon.
inorganic groups
inorganic group
inorganic groups
ChEBI
Any substituent group or skeleton containing carbon.
organic groups
organic group
organic groups
ChEBI
A univalent group formed by removing a hydrogen atom from a hydrocarbon.
hydrocarbyl group
hydrocarbyl groups
groupe hydrocarbyle
grupo hidrocarbilo
grupos hidrocarbilo
hydrocarbyl group
hydrocarbyl group
IUPAC
hydrocarbyl groups
IUPAC
groupe hydrocarbyle
IUPAC
grupo hidrocarbilo
IUPAC
grupos hidrocarbilo
IUPAC
Any organic substituent group, regardless of functional type, having one free valence at a carbon atom.
organyl group
organyl groups
groupe organyle
grupo organilo
grupos organilo
organyl group
organyl group
IUPAC
organyl groups
IUPAC
groupe organyle
IUPAC
grupo organilo
IUPAC
grupos organilo
IUPAC
A chemical entity constituting the smallest component of an element having the chemical properties of the element.
atom
atome
atomo
atoms
atomus
element
elements
atom
atom
IUPAC
atome
IUPAC
atomo
IUPAC
atoms
ChEBI
atomus
ChEBI
element
ChEBI
elements
ChEBI
atomic hydrogen
monoatomic hydrogen
atomic hydrogen
ChEBI
A nucleus is the positively charged central portion of an atom, excluding the orbital electrons.
nucleus
Atomkern
Kern
noyau
noyau atomique
nuclei
nucleo
nucleo atomico
nucleus atomi
atomic nucleus
nucleus
IUPAC
Atomkern
ChEBI
Kern
ChEBI
noyau
IUPAC
noyau atomique
ChEBI
nuclei
ChEBI
nucleo
IUPAC
nucleo atomico
ChEBI
nucleus atomi
ChEBI
Heavy nuclear particle: proton or neutron.
nucleon
Nukleon
Nukleonen
nucleons
nucleon
nucleon
IUPAC
nucleon
IUPAC
Nukleon
ChEBI
Nukleonen
ChEBI
nucleons
ChEBI
A derivative of an oxoacid RkE(=O)l(OH)m (l =/= 0) in which an acidic hydroxy group has been replaced by an amino or substituted amino group.
primary amide
primary amides
primary amide
primary amide
IUPAC
primary amides
IUPAC
A molecular entity all atoms of which have the same atomic number.
homoatomic entity
homoatomic molecular entities
homoatomic molecular entity
elemental molecular entity
homoatomic entity
ChEBI
homoatomic molecular entities
ChEBI
homoatomic molecular entity
ChEBI
elemental hydrogen
An organosulfur compound is a compound containing at least one carbon-sulfur bond.
organosulfur compound
organosulfur compounds
organosulfur compound
organosulfur compound
ChEBI
organosulfur compounds
ChEBI
elemental oxygen
diatomic oxygen
triatomic oxygen
An anion consisting of more than one atom.
polyatomic anions
polyatomic anion
polyatomic anions
ChEBI
chemical messenger
molecular messenger
chemical messenger
ChEBI
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
Antibiotika
Antibiotikum
antibiotic
antibiotics
antibiotique
antimicrobial
antimicrobial agents
antimicrobials
microbicide
microbicides
antimicrobial agent
Antibiotika
ChEBI
Antibiotikum
ChEBI
antibiotic
ChEBI
antibiotics
ChEBI
antibiotique
IUPAC
antimicrobial
ChEBI
antimicrobial agents
ChEBI
antimicrobials
ChEBI
microbicide
ChEBI
microbicides
ChEBI
A substance (or active part thereof) that kills or slows the growth of bacteria.
antibacterial agents
antibacterials
bactericide
bactericides
antibacterial agent
antibacterial agents
ChEBI
antibacterials
ChEBI
bactericide
ChEBI
bactericides
ChEBI
A nutrient is a food component that an organism uses to survive and grow.
nutrients
nutrient
nutrients
ChEBI
A heteroorganic entity is an organic molecular entity in which carbon atoms or organic groups are bonded directly to one or more heteroatoms.
heteroorganic entities
organoelement compounds
heteroorganic entity
heteroorganic entities
ChEBI
organoelement compounds
ChEBI
An agrochemical is a substance that is used in agriculture or horticulture.
agrichemical
agrichemicals
agricultural chemicals
agrochemicals
agrochemical
agrichemical
ChEBI
agrichemicals
ChEBI
agricultural chemicals
ChEBI
agrochemicals
ChEBI
A fertilizer is any substance that is added to soil or water to assist the growth of plants.
fertiliser
fertilizers
fertilizer
fertiliser
ChEBI
fertilizers
ChEBI
An energy-rich substance that can be transformed with release of usable energy.
fuel
A substance administered to aid diagnosis of a disease.
diagnostic aid
diagnostic agent
diagnostic aid
ChEBI
A molecular entity containing one or more atoms of an alkali metal.
alkali metal molecular entities
alkali metal molecular entity
alkali metal molecular entities
ChEBI
An alkaline earth molecular entity is a molecular entity containing one or more atoms of an alkaline earth metal.
alkaline earth molecular entity
alkaline earth compounds
alkaline earth molecular entities
alkaline-earth compounds
alkaline earth molecular entity
alkaline earth molecular entity
ChEBI
alkaline earth compounds
ChEBI
alkaline earth molecular entities
ChEBI
alkaline-earth compounds
ChEBI
Any p-block element atom that is in group 15 of the periodic table: nitrogen, phosphorus, arsenic, antimony and bismuth.
pnictogens
group 15 elements
group V elements
nitrogenoideos
nitrogenoides
pnictogene
pnictogenes
pnictogen
pnictogens
IUPAC
group 15 elements
ChEBI
group V elements
ChEBI
nitrogenoideos
ChEBI
nitrogenoides
ChEBI
pnictogene
ChEBI
pnictogenes
ChEBI
A p-block molecular entity containing any pnictogen.
pnictogen molecular entity
pnictogen molecular entities
pnictogen molecular entity
pnictogen molecular entity
ChEBI
pnictogen molecular entities
ChEBI
Any p-block element belonging to the group 16 family of the periodic table.
chalcogen
chalcogens
Chalkogen
Chalkogene
anfigeno
anfigenos
calcogeno
calcogenos
chalcogene
chalcogenes
group 16 elements
group VI elements
chalcogen
chalcogen
IUPAC
chalcogens
IUPAC
Chalkogen
ChEBI
Chalkogene
ChEBI
anfigeno
ChEBI
anfigenos
ChEBI
calcogeno
ChEBI
calcogenos
ChEBI
chalcogene
ChEBI
chalcogenes
ChEBI
group 16 elements
ChEBI
group VI elements
ChEBI
Any p-block molecular entity containing a chalcogen.
chalcogen molecular entity
chalcogen compounds
chalcogen molecular entities
chalcogen molecular entity
chalcogen molecular entity
ChEBI
chalcogen compounds
ChEBI
chalcogen molecular entities
ChEBI
group 14 elements
carbon group element
carbon group elements
carbonoides
cristallogene
cristallogenes
group IV elements
carbon group element atom
group 14 elements
IUPAC
carbon group element
ChEBI
carbon group elements
ChEBI
carbonoides
ChEBI
cristallogene
ChEBI
cristallogenes
ChEBI
group IV elements
ChEBI
An ester of a carboxylic acid, R(1)C(=O)OR(2), where R(1) = H or organyl and R(2) = organyl.
Carboxylic ester
carboxylic esters
a carboxylic ester
carboxylic acid esters
carboxylic ester
Carboxylic ester
KEGG_COMPOUND
carboxylic esters
IUPAC
a carboxylic ester
UniProt
carboxylic acid esters
ChEBI
group 13 elements
Element der Borgruppe
boron group element
boron group elements
group III elements
boron group element atom
group 13 elements
IUPAC
Element der Borgruppe
ChEBI
boron group element
ChEBI
boron group elements
ChEBI
group III elements
ChEBI
An atom belonging to one of the main groups (found in the s- and p- blocks) of the periodic table.
main group elements
Hauptgruppenelement
Hauptgruppenelemente
main group element
main group element atom
main group elements
IUPAC
Hauptgruppenelement
ChEBI
Hauptgruppenelemente
ChEBI
main group element
ChEBI
radium
88Ra
Ra
radio
radium
radium atom
radium
IUPAC
88Ra
IUPAC
Ra
IUPAC
radio
ChEBI
radium
ChEBI
A group derived from an arene by removal of a hydrogen atom from a ring carbon atom.
aryl groups
Arylgruppe
groupe aryle
grupos arilo
aryl group
aryl groups
IUPAC
Arylgruppe
ChEBI
groupe aryle
IUPAC
grupos arilo
IUPAC
group 12 elements
zinc group element
zinc group elements
zinc group element atom
group 12 elements
IUPAC
zinc group element
ChEBI
zinc group elements
ChEBI
group 6 elements
chromium group element
chromium group elements
chromium group element atom
group 6 elements
IUPAC
chromium group element
ChEBI
chromium group elements
ChEBI
group 7 elements
manganese group element
manganese group elements
manganese group element atom
group 7 elements
IUPAC
manganese group element
ChEBI
manganese group elements
ChEBI
group 8 elements
iron group element
iron group elements
iron group element atom
group 8 elements
IUPAC
iron group element
ChEBI
iron group elements
ChEBI
group 9 elements
cobalt group element
cobalt group elements
cobalt group element atom
group 9 elements
IUPAC
cobalt group element
ChEBI
cobalt group elements
ChEBI
group 10 elements
nickel group element
nickel group elements
nickel group element atom
group 10 elements
IUPAC
nickel group element
ChEBI
nickel group elements
ChEBI
platinum
78Pt
Platin
Pt
platine
platino
platinum
platinum
IUPAC
78Pt
IUPAC
Platin
ChEBI
Pt
IUPAC
platine
ChEBI
platino
ChEBI
PGM
Platinmetalle
Platinoide
platinoid
platinum group metal
platinum group metals
platinum metals
platinum group metal atom
PGM
ChEBI
Platinmetalle
ChEBI
Platinoide
ChEBI
platinoid
ChEBI
platinum group metal
ChEBI
platinum group metals
ChEBI
platinum metals
ChEBI
group 11 elements
coinage metals
copper group element
copper group elements
copper group element atom
group 11 elements
IUPAC
coinage metals
ChEBI
copper group element
ChEBI
copper group elements
ChEBI
oxoacids of sulfur
sulfur oxoacids
sulfur oxoacid
oxoacids of sulfur
ChEBI
sulfur oxoacids
ChEBI
A hydracid is a compound which contains hydrogen that is not bound to oxygen, and which produces a conjugate base by loss of positive hydrogen ion(s) (hydrons).
hydracid
hydracids
hydracid
hydracid
IUPAC
hydracids
ChEBI
pnictogen oxoacids
pnictogen oxoacid
pnictogen oxoacids
ChEBI
sulfur oxoacid derivative
sulfur oxoacid derivatives
sulfur oxoacid derivative
sulfur oxoacid derivative
ChEBI
sulfur oxoacid derivatives
ChEBI
monoatomic monoanions
monoatomic monoanion
monoatomic monoanions
ChEBI
elemental chlorine
atomic chlorine
monoatomic chlorine
atomic chlorine
ChEBI
monoatomic halogens
monoatomic halogen
monoatomic halogens
ChEBI
elemental halogen
elemental halogens
elemental halogen
elemental halogen
ChEBI
elemental halogens
ChEBI
Arylmethyl groups and derivatives formed by substitution: ArCR2-.
benzylic group
benzylic groups
benzylic groups
groupe benzylique
benzylic group
benzylic group
IUPAC
benzylic groups
IUPAC
benzylic groups
ChEBI
groupe benzylique
IUPAC
nitrogen oxoacids
oxoacids of nitrogen
nitrogen oxoacid
nitrogen oxoacids
ChEBI
oxoacids of nitrogen
ChEBI
A pnictogen oxoacid which contains phosphorus and oxygen, at least one hydrogen atom bound to oxygen, and forms an ion by the loss of one or more protons.
phosphorus oxoacid
Oxosaeure des Phosphors
oxoacids of phosphorus
phosphorus oxoacids
phosphorus oxoacid
phosphorus oxoacid
ChEBI
Oxosaeure des Phosphors
ChEBI
oxoacids of phosphorus
ChEBI
phosphorus oxoacids
ChEBI
nitrogen oxoanion
nitrogen oxoanions
oxoanions of nitrogen
nitrogen oxoanion
nitrogen oxoanion
ChEBI
nitrogen oxoanions
ChEBI
oxoanions of nitrogen
ChEBI
pnictogen oxoanion
pnictogen oxoanions
pnictogen oxoanion
pnictogen oxoanion
ChEBI
pnictogen oxoanions
ChEBI
phosphorus oxoanion
oxoanions of phosphorus
phosphorus oxoanions
phosphorus oxoanion
phosphorus oxoanion
ChEBI
oxoanions of phosphorus
ChEBI
phosphorus oxoanions
ChEBI
A monovalent inorganic anion obtained by deprotonation of one of the two OH groups in phosphonic acid.
hydridohydroxidodioxidophosphate(1-)
hydrogen phosphonate
[PHO2(OH)](-)
hydrogenphosphonate
phosphonate(1-)
hydridohydroxidodioxidophosphate(1-)
IUPAC
hydrogen phosphonate
IUPAC
[PHO2(OH)](-)
IUPAC
hydrogenphosphonate
IUPAC
A bivalent group formed by removing two hydrogen atoms from a hydrocarbon, the free valencies of which are not engaged in a double bond.
hydrocarbylene group
hydrocarbylene groups
groupe hydrocarbylene
grupo hidrocarbileno
grupos hidrocarbileno
hydrocarbylene group
hydrocarbylene group
IUPAC
hydrocarbylene groups
IUPAC
groupe hydrocarbylene
IUPAC
grupo hidrocarbileno
IUPAC
grupos hidrocarbileno
IUPAC
sulfur oxoanion
oxoanions of sulfur
sulfur oxoanions
sulfur oxoanion
sulfur oxoanion
ChEBI
oxoanions of sulfur
ChEBI
sulfur oxoanions
ChEBI
chalcogen oxoacid
chalcogen oxoacids
chalcogen oxoacid
chalcogen oxoacid
ChEBI
chalcogen oxoacids
ChEBI
chalcogen oxoanion
chalcogen oxoanions
chalcogen oxoanion
chalcogen oxoanion
ChEBI
chalcogen oxoanions
ChEBI
A molecular entity containing one or more atoms of a transition element.
transition element molecular entities
transition metal molecular entity
transition element molecular entity
transition element molecular entities
ChEBI
transition metal molecular entity
ChEBI
alkali metal cations
alkali metal cation
alkali metal cations
ChEBI
alkaline earth cations
alkaline earth metal cation
alkaline-earth metal cations
alkaline earth cation
alkaline earth cations
ChEBI
alkaline earth metal cation
ChEBI
alkaline-earth metal cations
ChEBI
transition element cations
transition metal cation
transition element cation
transition element cations
ChEBI
transition metal cation
ChEBI
An atom of an element that exhibits typical metallic properties, being typically shiny, with high electrical and thermal conductivity.
elemental metal
elemental metals
metal element
metal elements
metals
metal atom
elemental metal
ChEBI
elemental metals
ChEBI
metal element
ChEBI
metal elements
ChEBI
metals
ChEBI
The sulfur oxoanion formed by deprotonation of sulfonic acid.
hydridotrioxidosulfate(1-)
SHO3(-)
[SHO3](-)
sulfonates
sulfonate
hydridotrioxidosulfate(1-)
IUPAC
SHO3(-)
IUPAC
[SHO3](-)
IUPAC
sulfonates
ChEBI
An organic derivative of sulfonic acid in which the sulfo group is linked directly to carbon.
organosulfonic acids
sulfonic acids
organosulfonic acid
organosulfonic acids
ChEBI
sulfonic acids
ChEBI
sulfonic acid derivative
derivatives of sulfonic acid
sulfonic acid derivatives
sulfonic acid derivative
sulfonic acid derivative
ChEBI
derivatives of sulfonic acid
ChEBI
sulfonic acid derivatives
ChEBI
An organic anion obtained by deprotonation of the sufonate group(s) of any organosulfonic acid.
organosulfonate
organosulfonate oxoanions
organosulfonates
organosulfonate oxoanion
organosulfonate
ChEBI
organosulfonate oxoanions
ChEBI
organosulfonates
ChEBI
Organic derivatives of sulfonic acid in which the sulfo group is linked directly to carbon of an aryl group.
arenesulfonic acids
arylsulfonic acid
arylsulfonic acids
arenesulfonic acid
arenesulfonic acids
ChEBI
arylsulfonic acid
ChEBI
arylsulfonic acids
ChEBI
An amino-acid anion obtained by deprotonation of any alpha-amino acid.
alpha-amino-acid anion
alpha-amino acid anions
alpha-amino-acid anions
alpha-amino-acid anion
alpha-amino-acid anion
ChEBI
alpha-amino acid anions
ChEBI
alpha-amino-acid anions
ChEBI
s-block element
s-block elements
s-block element atom
s-block element
ChEBI
s-block elements
ChEBI
Any main group element atom belonging to the p-block of the periodic table.
p-block element
p-block elements
p-block element atom
p-block element
ChEBI
p-block elements
ChEBI
d-block element
d-block elements
d-block element atom
d-block element
ChEBI
d-block elements
ChEBI
benzenediols
A carbon oxoacid acid carrying at least one -C(=O)OH group and having the structure RC(=O)OH, where R is any any monovalent functional group. Carboxylic acids are the most common type of organic acid.
carboxylic acid
carboxylic acids
Carbonsaeure
Carbonsaeuren
Karbonsaeure
RC(=O)OH
acide carboxylique
acides carboxyliques
acido carboxilico
acidos carboxilicos
carboxylic acid
carboxylic acid
IUPAC
carboxylic acids
IUPAC
Carbonsaeure
ChEBI
Carbonsaeuren
ChEBI
Karbonsaeure
ChEBI
RC(=O)OH
IUPAC
acide carboxylique
IUPAC
acides carboxyliques
IUPAC
acido carboxilico
IUPAC
acidos carboxilicos
IUPAC
Any carboxylic acid having a sulfur substituent.
S-containing carboxylic acid
S-containing carboxylic acids
sulfur-containing carboxylic acids
sulfur-containing carboxylic acid
S-containing carboxylic acid
ChEBI
S-containing carboxylic acids
ChEBI
sulfur-containing carboxylic acids
ChEBI
A molecular entity containing one or more atoms from any of groups 1, 2, 13, 14, 15, 16, 17, and 18 of the periodic table.
main group compounds
main group molecular entities
main group molecular entity
main group compounds
ChEBI
main group molecular entities
ChEBI
boron group molecular entities
boron group molecular entity
boron group molecular entities
ChEBI
carbon group molecular entity
carbon group molecular entities
carbon group molecular entity
carbon group molecular entity
ChEBI
carbon group molecular entities
ChEBI
Any molecule that consists of a series of atoms joined together to form a ring.
cyclic compounds
cyclic compound
cyclic compounds
ChEBI
A cyclic compound having as ring members atoms of the same element only.
homocyclic compound
homocyclic compounds
isocyclic compounds
homocyclic compound
homocyclic compound
IUPAC
homocyclic compounds
IUPAC
isocyclic compounds
IUPAC
A homocyclic compound in which all of the ring members are carbon atoms.
carbocyclic compound
carbocyclic compounds
carbocycle
carbocyclic compound
carbocyclic compound
IUPAC
carbocyclic compounds
IUPAC
carbocycle
ChEBI
hydrogen compounds
hydrogen molecular entities
hydrogen molecular entity
hydrogen compounds
ChEBI
hydrogen molecular entities
ChEBI
boron oxoanion
boron oxoanions
boron oxoanion
boron oxoanion
ChEBI
boron oxoanions
ChEBI
polycyclic compounds
polycyclic compound
polycyclic compounds
ChEBI
A molecule that features two fused rings.
bicyclic compounds
bicyclic compound
bicyclic compounds
ChEBI
A polycyclic compound in which two rings have two, and only two, atoms in common. Such compounds have n common faces and 2n common atoms.
ortho-fused polycyclic compounds
ortho-fused compounds
ortho-fused compound
ortho-fused polycyclic compounds
IUPAC
ortho-fused compounds
ChEBI
Acyclic and cyclic hydrocarbons having one or more carbon-carbon double bonds, apart from the formal ones in aromatic compounds. The class olefins subsumes alkenes and cycloalkenes and the corresponding polyenes.
olefin
olefins
olefins
olefin
olefin
IUPAC
olefins
IUPAC
olefins
ChEBI
Acyclic branched or unbranched hydrocarbons having one or more carbon-carbon double bond.
acyclic olefins
acyclic olefin
acyclic olefins
ChEBI
Any acyclic or cyclic, saturated or unsaturated carbon compound, excluding aromatic compounds.
aliphatic compounds
aliphatic compound
aliphatic compounds
IUPAC
An aliphatic compound having a carbocyclic ring structure which may be saturated or unsaturated, but may not be a benzenoid or other aromatic system.
alicyclic compounds
alicyclic compound
alicyclic compounds
IUPAC
A cyclically conjugated molecular entity with a stability (due to delocalization) significantly greater than that of a hypothetical localized structure (e.g. Kekule structure) is said to possess aromatic character.
aromatic compounds
aromatic molecular entity
aromatics
aromatische Verbindungen
aromatic compound
aromatic compounds
IUPAC
aromatic molecular entity
IUPAC
aromatics
ChEBI
aromatische Verbindungen
ChEBI
Any monocyclic or polycyclic aromatic hydrocarbon.
arene
arenes
aromatic hydrocarbons
arene
arene
IUPAC
arenes
IUPAC
aromatic hydrocarbons
IUPAC
organic aromatic compounds
organic aromatic compound
organic aromatic compounds
ChEBI
monocyclic compounds
monocyclic compound
monocyclic compounds
ChEBI
A mancude monocyclic hydrocarbon without side chains of the general formula CnHn (n is an even number) or CnHn+1 (n is an odd number). In systematic nomenclature an annulene with seven or more carbon atoms may be named [n]annulene, where n is the number of carbon atoms.
annulene
annulenes
annulene
annulene
IUPAC
annulenes
IUPAC
cyclic hydrocarbon
cyclic hydrocarbons
cyclic hydrocarbon
cyclic hydrocarbon
ChEBI
cyclic hydrocarbons
ChEBI
monocyclic hydrocarbon
monocyclic hydrocarbons
monocyclic hydrocarbons
monocyclic hydrocarbon
monocyclic hydrocarbon
ChEBI
monocyclic hydrocarbons
IUPAC
monocyclic hydrocarbons
ChEBI
polycyclic hydrocarbon
polycyclic hydrocarbons
polycyclic hydrocarbon
polycyclic hydrocarbon
IUPAC
polycyclic hydrocarbons
IUPAC
heteromonocyclic compound
heteromonocyclic compounds
heteromonocyclic compound
heteromonocyclic compound
IUPAC
heteromonocyclic compounds
IUPAC
A polycyclic compound in which at least one of the rings contains at least one non-carbon atom.
heteropolycyclic compounds
polyheterocyclic compounds
heteropolycyclic compound
heteropolycyclic compounds
IUPAC
polyheterocyclic compounds
ChEBI
A bicyclic compound in which at least one of the rings contains at least one skeletal heteroatom.
heterobicyclic compounds
heterobicyclic compound
heterobicyclic compounds
IUPAC
zinc group molecular entities
zinc group molecular entity
zinc group molecular entities
ChEBI
An s-block molecular entity is a molecular entity containing one or more atoms of an s-block element.
s-block molecular entity
s-block compounds
s-block molecular entities
s-block molecular entity
s-block molecular entity
ChEBI
s-block compounds
ChEBI
s-block molecular entities
ChEBI
A main group molecular entity that contains one or more atoms of a p-block element.
p-block compounds
p-block molecular entities
p-block molecular entitiy
p-block molecular entity
p-block compounds
ChEBI
p-block molecular entities
ChEBI
p-block molecular entitiy
ChEBI
A d-block molecular entity is a molecular entity containing one or more atoms of a d-block element.
d-block molecular entity
d-block compounds
d-block molecular entities
d-block molecular entity
d-block molecular entity
ChEBI
d-block compounds
ChEBI
d-block molecular entities
ChEBI
Hydrides are chemical compounds of hydrogen with other chemical elements.
hydrides
oxygen hydride
hydrides of oxygen
oxygen hydrides
oxygen hydride
oxygen hydride
ChEBI
hydrides of oxygen
ChEBI
oxygen hydrides
ChEBI
A macromolecule formed by a living organism.
biopolymer
Biopolymere
biomacromolecules
biopolymers
biomacromolecule
biopolymer
IUPAC
Biopolymere
ChEBI
biomacromolecules
ChEBI
biopolymers
ChEBI
genetically encoded biomacromolecules
genetically encoded biopolymers
information biomacromolecules
information biopolymers
information macromolecule
information macromolecules
information biomacromolecule
genetically encoded biomacromolecules
ChEBI
genetically encoded biopolymers
ChEBI
information biomacromolecules
ChEBI
information biopolymers
ChEBI
information macromolecule
ChEBI
information macromolecules
ChEBI
A macromolecule made up of nucleotide units and hydrolysable into certain pyrimidine or purine bases (usually adenine, cytosine, guanine, thymine, uracil), D-ribose or 2-deoxy-D-ribose and phosphoric acid.
nucleic acids
NA
Nukleinsaeure
Nukleinsaeuren
acide nucleique
acides nucleiques
acido nucleico
acidos nucleicos
nucleic acid
nucleic acids
IUPAC
NA
ChEBI
Nukleinsaeure
ChEBI
Nukleinsaeuren
ChEBI
acide nucleique
ChEBI
acides nucleiques
ChEBI
acido nucleico
ChEBI
acidos nucleicos
ChEBI
canonical amino-acid residue
canonical amino-acid residues
common amino acid residues
proteinogenic amino-acid residues
standard amino acid residues
standard amino-acid residues
proteinogenic amino-acid residue
canonical amino-acid residue
ChEBI
canonical amino-acid residues
ChEBI
common amino acid residues
ChEBI
proteinogenic amino-acid residues
ChEBI
standard amino acid residues
ChEBI
standard amino-acid residues
ChEBI
A cation consisting of more than one atom.
polyatomic cations
polyatomic cation
polyatomic cations
ChEBI
amino-acid cation
amino acid cation
amino-acid cations
amino-acid cation
amino-acid cation
ChEBI
amino acid cation
ChEBI
amino-acid cations
ChEBI
An amino acid in which the amino group is located on the carbon atom at the position alpha to the carboxy group.
alpha-amino acid
Amino acid
Amino acids
alpha-amino acids
alpha-amino carboxylic acids
alpha-amino acid
alpha-amino acid
IUPAC
Amino acid
KEGG_COMPOUND
Amino acids
KEGG_COMPOUND
alpha-amino acids
ChEBI
alpha-amino acids
JCBN
alpha-amino carboxylic acids
IUPAC
When two or more amino acids combine to form a peptide, the elements of water are removed, and what remains of each amino acid is called an amino-acid residue.
amino-acid residue
amino acid residue
amino-acid residues
amino-acid residue
amino-acid residue
IUPAC
amino acid residue
ChEBI
amino-acid residues
JCBN
A carboxylic acid containing one or more amino groups.
Aminocarbonsaeure
Aminokarbonsaeure
Aminosaeure
amino acids
amino acid
Aminocarbonsaeure
ChEBI
Aminokarbonsaeure
ChEBI
Aminosaeure
ChEBI
amino acids
ChEBI
alpha-amino-acid residues
alpha-amino-acid residue
alpha-amino-acid residues
ChEBI
alpha-amino-acid cation
alpha-amino acid cations
alpha-amino-acid cations
alpha-amino-acid cation
alpha-amino-acid cation
ChEBI
alpha-amino acid cations
ChEBI
alpha-amino-acid cations
ChEBI
manganese group molecular entity
manganese group molecular entities
manganese group molecular entity
manganese group molecular entity
ChEBI
manganese group molecular entities
ChEBI
iron group molecular entity
iron group molecular entities
iron group molecular entity
iron group molecular entity
ChEBI
iron group molecular entities
ChEBI
copper group molecular entity
copper group molecular entities
copper group molecular entity
copper group molecular entity
ChEBI
copper group molecular entities
ChEBI
nickel group molecular entity
nickel group molecular entities
nickel group molecular entity
nickel group molecular entity
ChEBI
nickel group molecular entities
ChEBI
platinum molecular entity
platinum compounds
platinum molecular entities
platinum molecular entity
platinum molecular entity
ChEBI
platinum compounds
ChEBI
platinum molecular entities
ChEBI
canonical nucleoside residues
common nucleoside residues
nucleoside residue
standard nucleoside residues
canonical nucleoside residue
canonical nucleoside residues
ChEBI
common nucleoside residues
CBN
nucleoside residue
CBN
standard nucleoside residues
ChEBI
canonical deoxyribonucleoside residues
common 2'-deoxyribonucleoside residue
common 2'-deoxyribonucleoside residues
dN
dNuc
standard deoxyribonucleoside residues
canonical deoxyribonucleoside residue
canonical deoxyribonucleoside residues
ChEBI
common 2'-deoxyribonucleoside residue
CBN
common 2'-deoxyribonucleoside residues
CBN
dN
CBN
dNuc
CBN
standard deoxyribonucleoside residues
ChEBI
An organic compound having at least one hydroxy group attached to a carbon atom.
hydroxy compounds
organic alcohol
organic hydroxy compounds
organic hydroxy compound
hydroxy compounds
IUPAC
organic alcohol
ChEBI
organic hydroxy compounds
ChEBI
Any organic molecule that consists of atoms connected in the form of a ring.
organic cyclic compounds
organic cyclic compound
organic cyclic compounds
ChEBI
A heterocyclic compound formally derived from an arene by replacement of one or more methine (-C=) and/or vinylene (-CH=CH-) groups by trivalent or divalent heteroatoms, respectively, in such a way as to maintain the continuous pi-electron system characteristic of aromatic systems and a number of out-of-plane pi-electrons corresponding to the Hueckel rule (4n+2).
heteroarenes
hetarenes
heteroarene
heteroarenes
IUPAC
hetarenes
IUPAC
benzenoid aromatic compounds
benzenoid compound
benzenoid aromatic compound
benzenoid aromatic compounds
ChEBI
benzenoid compound
ChEBI
An N-glycosyl compound that has both a nucleobase, normally adenine, guanine, xanthine, thymine, cytosine or uracil, and either a ribose or deoxyribose as functional parents.
Nucleoside
nucleosides
a nucleoside
nucleosides
nucleoside
Nucleoside
KEGG_COMPOUND
nucleosides
IUPAC
a nucleoside
UniProt
nucleosides
ChEBI
A macromolecule is a molecule of high relative molecular mass, the structure of which essentially comprises the multiple repetition of units derived, actually or conceptually, from molecules of low relative molecular mass.
macromolecule
macromolecules
polymer
polymer molecule
polymers
macromolecule
macromolecule
IUPAC
macromolecules
ChEBI
polymer
ChEBI
polymer molecule
IUPAC
polymers
ChEBI
aromatic annulenes
aromatic annulene
aromatic annulenes
ChEBI
A monocyclic aromatic hydrocarbon.
monocyclic arenes
monocyclic arene
monocyclic arenes
ChEBI
A polycyclic aromatic hydrocarbon.
PAH
PAHs
polycyclic arenes
polycyclic aromatic hydrocarbons
polycyclic arene
PAH
ChEBI
PAHs
ChEBI
polycyclic arenes
ChEBI
polycyclic aromatic hydrocarbons
ChEBI
Organic aromatic compounds having one or more hydroxy groups attached to a benzene or other arene ring.
phenols
Aryl alcohol
a phenol
arenols
phenols
phenols
IUPAC
Aryl alcohol
KEGG_COMPOUND
a phenol
UniProt
arenols
IUPAC
An amino acid whose structure includes an aromatic ring.
Aromatic amino acid
aromatic amino acids
aromatic amino acid
Aromatic amino acid
KEGG_COMPOUND
aromatic amino acids
ChEBI
Any carboxylic acid in which the carboxy group is directly bonded to an aromatic ring.
aromatic carboxylic acids
aromatic carboxylic acid
aromatic carboxylic acids
ChEBI
An amino compound in which the amino group is linked directly to an aromatic system.
aromatic amines
aryl amine
aryl amines
arylamine
arylamines
aromatic amine
aromatic amines
ChEBI
aryl amine
ChEBI
aryl amines
ChEBI
arylamine
ChEBI
arylamines
ChEBI
transition element coordination entities
transition metal coordination compounds
transition metal coordination entities
transition element coordination entity
transition element coordination entities
ChEBI
transition metal coordination compounds
ChEBI
transition metal coordination entities
ChEBI
platinum coordination entity
platinum coordination compounds
platinum coordination entities
platinum coordination entity
platinum coordination entity
ChEBI
platinum coordination compounds
ChEBI
platinum coordination entities
ChEBI
A substance used in a chemical reaction to detect, measure, examine, or produce other substances.
reagent
reactif
reactivo
reagents
reagent
reagent
IUPAC
reactif
IUPAC
reactivo
IUPAC
reagents
ChEBI
metal-tetrapyrrole
metal-tetrapyrrole complex
metallotetrapyrroles
metallotetrapyrrole
metal-tetrapyrrole
ChEBI
metal-tetrapyrrole complex
ChEBI
metallotetrapyrroles
ChEBI
A hexose with a (potential) aldehyde group at one end.
aldohexose
aldohexoses
aldohexose
aldohexose
ChEBI
aldohexoses
ChEBI
Any nutrient required in large quantities by organisms throughout their life in order to orchestrate a range of physiological functions. Macronutrients are usually chemical elements (carbon, hydrogen, nitrogen, oxygen, phosphorus and sulfur) that humans consume in the largest quantities. Calcium, sodium, magnesium and potassium are sometimes included as macronutrients because they are required in relatively large quantities compared with other vitamins and minerals.
macronutrients
macronutrient
macronutrients
ChEBI
halide salts
halides
halide salt
halide salts
ChEBI
halides
ChEBI
magnesium coordination entity
magnesium coordination compounds
magnesium coordination entities
magnesium coordination entity
magnesium coordination entity
ChEBI
magnesium coordination compounds
ChEBI
magnesium coordination entities
ChEBI
metallic bases
metallic base
metallic bases
ChEBI
alkali metal base
alkali metal bases
alkali metal hydroxides
alkali metal hydroxide
alkali metal base
ChEBI
alkali metal bases
ChEBI
alkali metal hydroxides
ChEBI
The diethyl ester of sulfuric acid.
DES
Diaethylsulfat
Et2SO4
diethyl sulphate
diethyl tetraoxosulfate
diethylsulfate
ethyl sulfate
sulfuric acid diethyl ester
sulphuric acid diethyl ester
diethyl sulfate
DES
KEGG_COMPOUND
Diaethylsulfat
ChemIDplus
Et2SO4
ChEBI
diethyl sulphate
ChemIDplus
diethyl tetraoxosulfate
ChemIDplus
diethylsulfate
ChemIDplus
ethyl sulfate
ChEBI
sulfuric acid diethyl ester
ChemIDplus
sulphuric acid diethyl ester
NIST_Chemistry_WebBook
nitrogen hydrides
nitrogen hydride
nitrogen hydrides
ChEBI
Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
azanes
azane
azanes
ChEBI
elemental manganese
(6'R)-beta,epsilon-carotene
(+)-alpha-carotene
alpha-carotene (natural)
(6'R)-beta,epsilon-carotene
(6'R)-beta,epsilon-carotene
IUPAC
(+)-alpha-carotene
ChemIDplus
alpha-carotene (natural)
ChemIDplus
(6'S)-beta,epsilon-carotene
(6'S)-beta,epsilon-carotene
(6'S)-beta,epsilon-carotene
IUPAC
elemental calcium
Kalziumsalz
Kalziumsalze
calcium salts
calcium salt
Kalziumsalz
ChEBI
Kalziumsalze
ChEBI
calcium salts
ChEBI
acyclic carotene
acyclic carotenes
acyclic carotene
acyclic carotene
ChEBI
acyclic carotenes
ChEBI
cyclic carotene
cyclic carotenes
cyclic carotene
cyclic carotene
ChEBI
cyclic carotenes
ChEBI
sulfate salts
sulfates
sulphate salts
sulphates
sulfate salt
sulfate salts
ChEBI
sulfates
ChEBI
sulphate salts
ChEBI
sulphates
ChEBI
A metal sulfate compound having zinc(2+) as the counterion.
zinc sulfate
ZnSO4
zinc sulfate (1:1)
zinc sulfate anhydrous
zinc sulphate
zinc(2+) sulfate
zinc(II) sulfate
zinc sulfate
zinc sulfate
IUPAC
ZnSO4
IUPAC
zinc sulfate (1:1)
ChemIDplus
zinc sulfate anhydrous
ChemIDplus
zinc sulphate
ChemIDplus
zinc(2+) sulfate
IUPAC
zinc(II) sulfate
IUPAC
A hydrocarbon of biological origin having carbon skeleton formally derived from isoprene [CH2=C(CH3)CH=CH2].
terpene
terpenes
Terpen
terpenes
terpeno
terpenos
terpene
terpene
IUPAC
terpenes
IUPAC
Terpen
ChEBI
terpenes
IUPAC
terpeno
IUPAC
terpenos
IUPAC
A C15 terpene.
sesquiterpenes
Sesquiterpen
sesquiterpenes
sesquiterpeno
sesquiterpenos
sesquiterpene
sesquiterpenes
IUPAC
Sesquiterpen
ChEBI
sesquiterpenes
IUPAC
sesquiterpeno
IUPAC
sesquiterpenos
IUPAC
A C20 terpene.
diterpenes
Diterpen
diterpenes
diterpeno
diterpenos
diterpene
diterpenes
IUPAC
Diterpen
ChEBI
diterpenes
IUPAC
diterpeno
IUPAC
diterpenos
IUPAC
A C40 terpene.
tetraterpenes
tetraterpenes
tetraterpeno
tetraterpenos
tetraterpene
tetraterpenes
IUPAC
tetraterpenes
IUPAC
tetraterpeno
IUPAC
tetraterpenos
IUPAC
A substance which lowers the surface tension of the medium in which it is dissolved, and/or the interfacial tension with other phases, and, accordingly, is positively adsorbed at the liquid/vapour and/or at other interfaces.
surfactant
surface active agent
surfactants
surfactant
surfactant
IUPAC
surface active agent
IUPAC
surfactants
ChEBI
A role played by a foreign substance mixed with or attached to a given substance to enable the distribution or location of the latter to be determined subsequently.
tracer
tracer
tracer
IUPAC
A role played by a part of a molecular entity distinguishable by the observer but not by the system and used to identify a tracer.
label
label
label
IUPAC
alkaline earth coordination entity
alkaline earth coordination compounds
alkaline earth coordination entities
alkaline earth coordination entity
alkaline earth coordination entity
ChEBI
alkaline earth coordination compounds
ChEBI
alkaline earth coordination entities
ChEBI
Any flavonoid that is a glycoside derivative of an anthocyanidin cation.
anthocyanins
anthocyanin cations
anthocyanin cation
anthocyanins
IUPAC
anthocyanin cations
ChEBI
plant growth inhibitor
plant growth inhibitors
plant growth retardants
plant growth retardant
plant growth inhibitor
ChEBI
plant growth inhibitors
ChEBI
plant growth retardants
ChEBI
A substance which is structurally similar to a metabolite but which competes with it or replaces it, and so prevents or reduces its normal utilization.
antimetabolite
antimetabolites
antimetabolite
antimetabolite
IUPAC
antimetabolites
ChEBI
A substance that diminishes the rate of a chemical reaction.
inhibitor
inhibidor
inhibiteur
inhibitors
inhibitor
inhibitor
IUPAC
inhibidor
ChEBI
inhibiteur
ChEBI
inhibitors
ChEBI
A substance that increases the rate of a reaction without modifying the overall standard Gibbs energy change in the reaction.
catalyst
Katalysator
catalizador
catalyseur
catalyst
catalyst
IUPAC
Katalysator
ChEBI
catalizador
ChEBI
catalyseur
ChEBI
2-ammonio-3-sulfanylpropanoate
cysteine zwitterion
(+)H3N-CH(CH2SH)-COO(-)
2-ammonio-3-mercaptopropanoate
cysteine zwitterion
2-ammonio-3-sulfanylpropanoate
IUPAC
cysteine zwitterion
IUPAC
(+)H3N-CH(CH2SH)-COO(-)
ChEBI
2-ammonio-3-mercaptopropanoate
ChEBI
The zwitterionic form of an amino acid having a negatively charged carboxyl group and a positively charged amino group.
amino acid zwitterion
amino acid zwitterion
amino acid zwitterion
ChEBI
A derivative of ammonium, NH4(+), in which one (or more) of the hydrogens bonded to the nitrogen have been replaced with univalent organyl groups. The substituting carbon of the organyl group must not itself be directly attached to a heteroatom (thereby excluding protonated amides, hemiaminals, etc).
ammonium ion derivatives
azanium ion derivative
azanium ion derivatives
ammonium ion derivative
ammonium ion derivatives
ChEBI
azanium ion derivative
ChEBI
azanium ion derivatives
ChEBI
Compounds (NH4(+))Y(-) and derivatives, in which one or more of the hydrogens bonded to nitrogen have been replaced with univalent groups.
azanium compounds
ammonium compounds
ammonium compound
azanium compounds
IUPAC
ammonium compounds
ChEBI
ammonium compounds
IUPAC
Cations of structure R2C=N(+)R2.
iminium ion
iminium cations
iminium ions
iminium ion
iminium ion
ChEBI
iminium cations
ChEBI
iminium ions
ChEBI
fused compounds
fused polycyclic compounds
fused-ring polycyclic compound
fused-ring polycyclic compounds
polycyclic fused-ring compounds
fused compound
fused compounds
ChEBI
fused polycyclic compounds
ChEBI
fused-ring polycyclic compound
ChEBI
fused-ring polycyclic compounds
ChEBI
polycyclic fused-ring compounds
ChEBI
A polyclic compound in which all of the ring members are carbon atoms.
carbopolycyclic compounds
carbopolycyclic compound
carbopolycyclic compounds
ChEBI
homopolycyclic compounds
homopolycyclic compound
homopolycyclic compounds
ChEBI
ortho-fused polycyclic arenes
ortho-fused polycyclic arene
ortho-fused polycyclic arenes
ChEBI
Dibenz[a,h]anthracene
1,2:5,6-Dibenzanthracene
DBA
dibenz[a,h]anthracene
Dibenz[a,h]anthracene
KEGG_COMPOUND
1,2:5,6-Dibenzanthracene
KEGG_COMPOUND
DBA
ChemIDplus
epoxycarotenoid
epoxycarotenols
epoxycarotenol
epoxycarotenoid
ChEBI
epoxycarotenols
ChEBI
Any drug that enhances the activity of the central nervous system.
central nervous system stimulant
CNS stimulant
analeptic
analeptic agent
analeptic drug
analeptics
central stimulant
central nervous system stimulant
central nervous system stimulant
ChEBI
CNS stimulant
ChEBI
analeptic
ChEBI
analeptic agent
ChEBI
analeptic drug
ChEBI
analeptics
ChEBI
central stimulant
ChEBI
Any of naturally occurring compounds and synthetic analogues, based on the cyclopenta[a]phenanthrene carbon skeleton, partially or completely hydrogenated; there are usually methyl groups at C-10 and C-13, and often an alkyl group at C-17. By extension, one or more bond scissions, ring expansions and/or ring contractions of the skeleton may have occurred. Natural steroids are derived biogenetically from squalene which is a triterpene.
Steroid
steroids
a steroid
steroid
Steroid
KEGG_COMPOUND
steroids
IUPAC
a steroid
UniProt
Hydroxysteroid
hydroxy steroids
hydroxysteroids
hydroxy steroid
Hydroxysteroid
KEGG_COMPOUND
hydroxy steroids
ChEBI
hydroxysteroids
ChEBI
Any heteroorganic entity containing at least one carbon-nitrogen bond.
organonitrogen compounds
organonitrogens
organonitrogen compound
organonitrogen compounds
IUPAC
organonitrogens
ChEBI
Compounds having the structure RC(=NR)NR2. The term is used as a suffix in systematic nomenclature to denote the -C(=NH)NH2 group including its carbon atom.
carboxamidines
Amidines
carboxamidines
carboxamidine
carboxamidines
IUPAC
Amidines
KEGG_COMPOUND
carboxamidines
ChEBI
Any aliphatic monocarboxylic acid derived from or contained in esterified form in an animal or vegetable fat, oil or wax. Natural fatty acids commonly have a chain of 4 to 28 carbons (usually unbranched and even-numbered), which may be saturated or unsaturated. By extension, the term is sometimes used to embrace all acyclic aliphatic carboxylic acids.
Fatty acid
fatty acids
Fettsaeure
Fettsaeuren
acide gras
acides gras
acido graso
acidos grasos
fatty acids
fatty acid
Fatty acid
KEGG_COMPOUND
fatty acids
IUPAC
Fettsaeure
ChEBI
Fettsaeuren
ChEBI
acide gras
ChEBI
acides gras
ChemIDplus
acido graso
ChEBI
acidos grasos
ChEBI
fatty acids
ChEBI
Parent monosaccharides are polyhydroxy aldehydes H[CH(OH)]nC(=O)H or polyhydroxy ketones H-[CHOH]n-C(=O)[CHOH]m-H with three or more carbon atoms. The generic term 'monosaccharide' (as opposed to oligosaccharide or polysaccharide) denotes a single unit, without glycosidic connection to other such units. It includes aldoses, dialdoses, aldoketoses, ketoses and diketoses, as well as deoxy sugars, provided that the parent compound has a (potential) carbonyl group.
Monosaccharide
monosaccharides
Monosaccharid
Monosacharid
monosacarido
monosacaridos
monosaccharide
Monosaccharide
KEGG_COMPOUND
monosaccharides
IUPAC
Monosaccharid
ChEBI
Monosacharid
ChEBI
monosacarido
ChEBI
monosacaridos
IUPAC
An alpha-amino-acid anion that is the conjugate base of aspartic acid.
aspartate(1-)
hydrogen aspartate
2-ammoniobutanedioate
2-ammoniosuccinate
aspartic acid monoanion
aspartate(1-)
aspartate(1-)
JCBN
hydrogen aspartate
IUPAC
2-ammoniobutanedioate
IUPAC
2-ammoniosuccinate
ChEBI
aspartic acid monoanion
JCBN
An oxoanion is an anion derived from an oxoacid by loss of hydron(s) bound to oxygen.
oxoanion
oxoacid anions
oxoanions
oxoanion
oxoanion
ChEBI
oxoacid anions
ChEBI
oxoanions
ChEBI
ortho-fused bicyclic arene
ortho-fused bicyclic arenes
ortho-fused bicyclic arene
ortho-fused bicyclic arene
ChEBI
ortho-fused bicyclic arenes
ChEBI
ortho-fused polycyclic hydrocarbon
ortho-fused polycyclic hydrocarbons
ortho-fused polycyclic hydrocarbon
ortho-fused polycyclic hydrocarbon
ChEBI
ortho-fused polycyclic hydrocarbons
ChEBI
ortho-fused bicyclic hydrocarbon
ortho-fused bicyclic hydrocarbons
ortho-fused bicyclic hydrocarbon
ortho-fused bicyclic hydrocarbon
ChEBI
ortho-fused bicyclic hydrocarbons
ChEBI
A substance used in the prophylaxis or therapy of infectious diseases.
anti-infective agents
anti-infective drugs
antiinfective agents
antiinfective drug
antiinfective agent
anti-infective agents
ChEBI
anti-infective drugs
ChEBI
antiinfective agents
ChEBI
antiinfective drug
ChEBI
A substance used to treat or prevent parasitic infections.
antiparasitic drugs
antiparasitics
parasiticides
antiparasitic agent
antiparasitic drugs
ChEBI
antiparasitics
ChEBI
parasiticides
ChEBI
Substance intended to kill parasitic worms (helminths).
anthelminthic
anthelminthics
anthelmintic
anthelmintics
antihelminth
antihelmintico
vermifuge
anthelminthic drug
anthelminthic
IUPAC
anthelminthics
ChEBI
anthelmintic
IUPAC
anthelmintics
ChEBI
antihelminth
ChEBI
antihelmintico
ChEBI
vermifuge
ChEBI
A substance used in the treatment or control of nematode infestations.
antinematodal agent
antinematodal drugs
antinematodals
antinematodal drug
antinematodal agent
ChEBI
antinematodal drugs
ChEBI
antinematodals
ChEBI
A cadmium coordination entity in which cadmium(2+) and Cl(-) ions are present in the ratio 2:1. Although considered to be ionic, it has considerable covalent character to its bonding.
cadmium dichloride
cadmium(2+) chloride
cadmium(II) chloride
Caddy
CdCl2
Dichlorocadmium
Kadmiumchlorid
[CdCl2]
cadmium chloride
cadmium dichloride
cadmium dichloride
IUPAC
cadmium(2+) chloride
IUPAC
cadmium(II) chloride
IUPAC
Caddy
ChemIDplus
CdCl2
IUPAC
Dichlorocadmium
ChemIDplus
Kadmiumchlorid
NIST_Chemistry_WebBook
[CdCl2]
MolBase
cadmium chloride
ChemIDplus
A class of drugs producing both physiological and psychological effects through a variety of mechanisms involving the central nervous system.
CNS agent
CNS drugs
central nervous system agents
central nervous system drug
CNS agent
ChEBI
CNS drugs
ChEBI
central nervous system agents
ChEBI
A loosely defined grouping of drugs that have effects on psychological function.
psychoactive agent
psychoactive drugs
psychopharmaceuticals
psychotropic drugs
psychotropic drug
psychoactive agent
ChEBI
psychoactive drugs
ChEBI
psychopharmaceuticals
ChEBI
psychotropic drugs
ChEBI
alkali metal salts
alkali metal salt
alkali metal salts
ChEBI
An agent capable of relieving pain without the loss of consciousness or without producing anaesthesia. In addition, analgesic is a role played by a compound which is exhibited by a capability to cause a reduction of pain symptoms.
analgesic
A drug that has principally analgesic, antipyretic and anti-inflammatory actions. Non-narcotic analgesics do not bind to opioid receptors.
non-narcotic analgesic
An agent that promotes the excretion of urine through its effects on kidney function.
diuretics
diuretic
diuretics
ChEBI
An addition compound contains two or more simpler compounds that can be packed in a definite ratio into a crystal. The term covers donor-acceptor complexes (adducts) and a variety of lattice compounds.
addition compounds
addition compound
addition compounds
ChEBI
natural product fundamental parents
natural product fundamental parent
natural product fundamental parents
IUPAC
heterocyclic parent hydrides
heterocyclic fundamental parent
heterocyclic organic fundamental parents
organic heterocyclic fundamental parents
heterocyclic organic fundamental parent
heterocyclic parent hydrides
IUPAC
heterocyclic fundamental parent
ChEBI
heterocyclic organic fundamental parents
ChEBI
organic heterocyclic fundamental parents
ChEBI
A drug that affects the rate or intensity of cardiac contraction, blood vessel diameter or blood volume.
cardiovascular agent
cardiovascular drugs
cardiovascular drug
cardiovascular agent
ChEBI
cardiovascular drugs
ChEBI
Any molecular entity that consists of a ring having (formally) the maximum number of noncumulative double bonds.
mancude-ring systems
mancude rings
mancunide-ring systems
mancude ring
mancude-ring systems
IUPAC
mancude rings
ChEBI
mancunide-ring systems
IUPAC
mancude organic heterobicyclic parents
mancude-ring organic heterobicyclic parents
mancude organic heterobicyclic parent
mancude organic heterobicyclic parents
ChEBI
mancude-ring organic heterobicyclic parents
ChEBI
mancude organic heterocyclic parents
mancude-ring organic heterocyclic parents
mancude organic heterocyclic parent
mancude organic heterocyclic parents
ChEBI
mancude-ring organic heterocyclic parents
ChEBI
organic mancude parents
organic mancude-ring parents
organic mancude parent
organic mancude parents
ChEBI
organic mancude-ring parents
ChEBI
A heterobicyclic aromatic organic compound comprising a pyrimidine ring fused to an imidazole ring; the parent compound of the purines.
purine
purine
purine
IUPAC
The 1H-tautomer of purine.
1H-purine
1H-purine
1H-purine
ChEBI
The 3H-tautomer of purine.
3H-purine
3H-purine
3H-purine
IUPAC
The 9H-tautomer of purine.
9H-purine
9H-purine
9H-purine
IUPAC
9H-purine
UniProt
A simplest member of the class of chromene in which the heterocyclic pyran ring has a double bond between positions 3 and 4.
2H-chromene
1,2-benzopyran
2H-1-benzopyran
3-chromene
Delta-3-chromene
2H-chromene
2H-chromene
IUPAC
1,2-benzopyran
ChemIDplus
2H-1-benzopyran
ChemIDplus
3-chromene
NIST_Chemistry_WebBook
Delta-3-chromene
NIST_Chemistry_WebBook
chromene
chromene
chromene
IUPAC
A simplest member of the class of chromene in which the heterocyclic pyran ring has a double bond between positions 2 and 3.
4H-chromene
4H-1-benzopyran
4H-chromene
4H-chromene
IUPAC
4H-1-benzopyran
NIST_Chemistry_WebBook
A negative ion consisting solely of carbon and oxygen atoms, and therefore having the general formula CxOy(n-) for some integers x, y and n.
carbon oxoanion
carbon oxoanions
oxocarbon anion
oxocarbon anions
carbon oxoanion
carbon oxoanion
ChEBI
carbon oxoanions
ChEBI
oxocarbon anion
ChEBI
oxocarbon anions
ChEBI
carbon oxoacids
oxoacids of carbon
carbon oxoacid
carbon oxoacids
ChEBI
oxoacids of carbon
ChEBI
A substance that inhibits or prevents the proliferation of neoplasms.
anticancer agent
anticancer agents
antineoplastic
antineoplastic agents
cytostatic
antineoplastic agent
anticancer agent
ChEBI
anticancer agents
ChEBI
antineoplastic
ChEBI
antineoplastic agents
ChEBI
cytostatic
ChEBI
A food additive that is used to added improve the taste or odour of a food.
flavoring agent
flavoring agents
flavour enhancer
flavour enhancers
flavouring agents
flavouring agent
flavoring agent
ChEBI
flavoring agents
ChEBI
flavour enhancer
ChEBI
flavour enhancers
ChEBI
flavouring agents
ChEBI
Any ether in which the oxygen is attached to at least one aryl substituent.
aromatic ether
A drug used to cause dilation of the blood vessels.
vasodilator
vasodilator agents
vasodilator agent
vasodilator
ChEBI
vasodilator agents
ChEBI
A monocarboxylic acid that is naphthalene substituted by a carboxymethyl group at any position.
naphthalenylacetic acid
naphthylacetic acid
naphthalenylacetic acid
IUPAC
terpenoid fundamental parents
terpenoid fundamental parent
terpenoid fundamental parents
ChEBI
A secondary alcohol is a compound in which a hydroxy group, -OH, is attached to a saturated carbon atom which has two other carbon atoms attached to it.
Secondary alcohol
R-CHOH-R'
a secondary alcohol
secondary alcohols
secondary alcohol
Secondary alcohol
KEGG_COMPOUND
R-CHOH-R'
KEGG_COMPOUND
a secondary alcohol
UniProt
secondary alcohols
ChEBI
A member of the class of naphthols carrying a single hydroxy substituent at C-1 or C-2. A closed class.
naphthalenol
naphthol
hydroxynaphthalene
naphthol
naphthalenol
IUPAC
naphthol
IUPAC
hydroxynaphthalene
ChEBI
An agent used to treat cestode, trematode, or other flatworm infestations in man or animals.
antiplatyhelmintic agent
antiplatyhelmintic drugs
antiplatyhelmintic drug
antiplatyhelmintic agent
ChEBI
antiplatyhelmintic drugs
ChEBI
Any carboxylic acid containing two carboxy groups.
Dicarboxylic acid
dicarboxylic acids
dicarboxylic acid
Dicarboxylic acid
KEGG_COMPOUND
dicarboxylic acids
ChEBI
dicarboxylic acid anion
dicarboxylic acid anions
dicarboxylic acid anion
dicarboxylic acid anion
ChEBI
dicarboxylic acid anions
ChEBI
A compound formally derived from an oxoacid RkE(=O)l(OH)m (l > 0) and an alcohol, phenol, heteroarenol, or enol by linking with formal loss of water from an acidic hydroxy group of the former and a hydroxy group of the latter.
Ester
esters
ester
Ester
KEGG_COMPOUND
esters
ChEBI
An ether in which the oxygen atom is linked to two ethyl groups.
1,1'-oxydiethane
Diethyl ether
1,1'-oxybisethane
3-oxapentane
Aether
Anesthetic ether
Diethylaether
Ether
Pronarcol
R-610
aether
aether pro narcosi
diethyl oxide
ethoxyethane
ethyl ether
ethyl oxide
diethyl ether
1,1'-oxydiethane
IUPAC
Diethyl ether
KEGG_COMPOUND
1,1'-oxybisethane
ChemIDplus
3-oxapentane
ChemIDplus
Aether
ChEBI
Anesthetic ether
KEGG_COMPOUND
Diethylaether
ChEBI
Ether
KEGG_COMPOUND
Pronarcol
NIST_Chemistry_WebBook
R-610
ChEBI
aether
NIST_Chemistry_WebBook
aether pro narcosi
ChEBI
diethyl oxide
ChemIDplus
ethoxyethane
ChemIDplus
ethyl ether
ChemIDplus
ethyl oxide
ChemIDplus
A xenobiotic (Greek, xenos "foreign"; bios "life") is a compound that is foreign to a living organism. Principal xenobiotics include: drugs, carcinogens and various compounds that have been introduced into the environment by artificial means.
Xenobiotic
xenobiotic
xenobiotics
xenobiotic compounds
xenobiotic
Xenobiotic
KEGG_COMPOUND
xenobiotic
IUPAC
xenobiotics
IUPAC
xenobiotic compounds
ChEBI
An agent that suppresses immune function by one of several mechanisms of action. Classical cytotoxic immunosuppressants act by inhibiting DNA synthesis. Others may act through activation of T-cells or by inhibiting the activation of helper cells. In addition, an immunosuppressive agent is a role played by a compound which is exhibited by a capability to diminish the extent and/or voracity of an immune response.
immunosuppressant
immunosuppressive agents
inmunosupresor
immunosuppressive agent
immunosuppressant
ChEBI
immunosuppressive agents
ChEBI
inmunosupresor
ChEBI
A compound having a nitro group, -NO2 (free valence on nitrogen), which may be attached to carbon, nitrogen (as in nitramines), or oxygen (as in nitrates), among other elements (in the absence of specification, C-nitro compounds are usually implied).
nitro compounds
nitro compound
nitro compounds
IUPAC
An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
antifungal
antifungal agents
antifungal drug
antifungal drugs
antifungals
antifungal agent
antifungal
ChEBI
antifungal agents
ChEBI
antifungal drug
ChEBI
antifungal drugs
ChEBI
antifungals
ChEBI
Any member of the group of lipids containing a common glycerol backbone to which at least one fatty acid-derived group is attached.
glycerolipids
glycerolipid
glycerolipids
ChEBI
A carboxylic acid anion formed when the carboxy group of a monocarboxylic acid is deprotonated.
Carboxylate
Monocarboxylate
a monocarboxylate
monocarboxylates
monocarboxylic acid anions
monocarboxylic acid anion
Carboxylate
KEGG_COMPOUND
Monocarboxylate
KEGG_COMPOUND
a monocarboxylate
UniProt
monocarboxylates
ChEBI
monocarboxylic acid anions
ChEBI
A phosphorus oxoanion that is the conjugate base of phosphoric acid.
Pi
phosphate
phosphate ions
phosphate ion
Pi
ChEBI
phosphate
ChEBI
phosphate ions
ChEBI
Compounds having the nitroso group, -NO, attached to carbon, or to another element, most commonly nitrogen or oxygen.
nitroso compounds
nitroso compound
nitroso compounds
ChEBI
nitroso
-N=O
O=N-
nitroso group
nitroso
IUPAC
-N=O
IUPAC
O=N-
IUPAC
N-Nitroso amines, compounds of the structure R2NNO. Compounds RNHNO are not ordinarily isolable, but they, too, are nitrosamines. The name is a contraction of N-nitrosoamine and, as such, does not require the N locant.
N-Nitroso amines
nitrosamines
nitrosamine
N-Nitroso amines
IUPAC
nitrosamines
ChEBI
N-Nitrosodimethylamine
N-methyl-N-nitrosomethanamine
1,1-Dimethyl-2-oxohydrazine
DMN
Dimethylnitrosamine
Dimethylnitrosoamine
N,N-Dimethylnitrosamine
N-nitrosodimethylamine
N-Nitrosodimethylamine
ChemIDplus
N-Nitrosodimethylamine
KEGG_COMPOUND
N-methyl-N-nitrosomethanamine
IUPAC
1,1-Dimethyl-2-oxohydrazine
NIST_Chemistry_WebBook
DMN
ChemIDplus
Dimethylnitrosamine
KEGG_COMPOUND
Dimethylnitrosoamine
ChemIDplus
N,N-Dimethylnitrosamine
ChemIDplus
Any antimicrobial drug which is used to treat or prevent protozoal infections.
antiprotozoal agent
antiprotozoal agents
antiprotozoal drugs
antiprotozoal drug
antiprotozoal agent
ChEBI
antiprotozoal agents
ChEBI
antiprotozoal drugs
ChEBI
A compound or agent that combines with lipoxygenase and thereby prevents its substrate-enzyme combination with arachidonic acid and the formation of the icosanoid products hydroxyicosatetraenoic acid and various leukotrienes.
lipooxygenase inhibitor
lipoxygenase inhibitors
lipoxygenase inhibitor
lipooxygenase inhibitor
ChEBI
lipoxygenase inhibitors
ChEBI
Any monocarboxylic acid which also contains a separate (alcoholic or phenolic) hydroxy substituent.
hydroxy acid
hydroxy monocarboxylic acids
hydroxy monocarboxylic acid
hydroxy acid
ChEBI
hydroxy monocarboxylic acids
ChEBI
Any monocarboxylic acid having at least one additional oxo functional group.
oxo monocarboxylic acids
oxo monocarboxylic acid
oxo monocarboxylic acids
ChEBI
imidazopyrimidines
imidazopyrimidine
imidazopyrimidines
ChEBI
pnictogen hydride
pnictogen hydrides
pnictogen hydride
pnictogen hydride
ChEBI
pnictogen hydrides
ChEBI
Phosphane (PH3) and compounds derived from it by substituting one, two or three hydrogen atoms by hydrocarbyl groups: RPH2, R2PH, R3P (R =/= H) are called primary, secondary and tertiary phosphines, respectively. A specific phosphine is preferably named as a substituted phosphane.
phosphines
fosfinas
phosphines
phosphine
phosphines
IUPAC
fosfinas
IUPAC
phosphines
ChEBI
A compound derived from phosphane by substituting one hydrogen atom by a hydrocarbyl group.
primary phosphines
fosfina primaria
fosfinas primarias
phospnines primaires
primary phosphine
primary phosphines
IUPAC
fosfina primaria
IUPAC
fosfinas primarias
IUPAC
phospnines primaires
IUPAC
ethylphosphane
EtPH2
Ethylphosphin
ethylphosphine
ethylphosphane
IUPAC
EtPH2
ChEBI
Ethylphosphin
ChEBI
oxo monocarboxylic acid anions
oxo monocarboxylic acid anion
oxo monocarboxylic acid anions
ChEBI
Any carboxylic acid anion containing at least one oxo group.
oxo carboxylic acid anions
oxo carboxylic acid anion
oxo carboxylic acid anions
ChEBI
A monosubstitution product of hydrogen peroxide, HOOH.
hydroperoxide
hydroperoxides
hydroperoxide
hydroperoxide
ChEBI
hydroperoxides
ChEBI
Monosubstitution products of hydrogen peroxide HOOH, having the skeleton ROOH, in which R is any organyl group.
peroxols
a hydroperoxide
hydroperoxides
organic hydroperoxides
peroxols
peroxol
peroxols
IUPAC
a hydroperoxide
UniProt
hydroperoxides
IUPAC
organic hydroperoxides
ChEBI
peroxols
ChEBI
A substance used for its pharmacological action on any aspect of neurotransmitter systems. Neurotransmitter agents include agonists, antagonists, degradation inhibitors, uptake inhibitors, depleters, precursors, and modulators of receptor function.
neurotransmitter agents
neurotransmitter agent
neurotransmitter agents
ChEBI
5-oxo monocarboxylic acid anions
5-oxo monocarboxylic acid anion
5-oxo monocarboxylic acid anions
ChEBI
A family of polyunsaturated fatty acids that have in common a final carbon-carbon double bond in the n-6 position, i.e., the sixth bond from the methyl end of the fatty acid.
omega-6 fatty acid
omega-6 fatty acids
omega-6 fatty acid
omega-6 fatty acid
ChEBI
omega-6 fatty acids
ChEBI
A chloroalkane that is ethane in which one or more of the hydrogens is replaced by chlorine.
chloroethanes
An octadecenoic acid with a double bond at C-9.
octadec-9-enoic acid
18:1, n-9
9-octadecenoic acid
C18:1, n-9
Delta(9)-octadecenoic acid
octadec-9-enoic acid
octadec-9-enoic acid
IUPAC
18:1, n-9
ChEBI
9-octadecenoic acid
ChEBI
C18:1, n-9
ChEBI
Delta(9)-octadecenoic acid
ChemIDplus
A drug used to treat or prevent microbial infections.
antimicrobial drugs
antimicrobial drug
antimicrobial drugs
ChEBI
Any monocarboxylic acid anion carrying at least one hydroxy substituent.
hydroxy monocarboxylic acid anions
hydroxymonocarboxylic acid anion
hydroxymonocarboxylic acid anions
hydroxy monocarboxylic acid anion
hydroxy monocarboxylic acid anions
ChEBI
hydroxymonocarboxylic acid anion
ChEBI
hydroxymonocarboxylic acid anions
ChEBI
A biological macromolecule minimally consisting of one polypeptide chain synthesized at the ribosome.
proteins
protein
proteins
IUPAC
inorganic chloride salt
inorganic chloride salts
inorganic chlorides
inorganic chloride
inorganic chloride salt
ChEBI
inorganic chloride salts
ChEBI
inorganic chlorides
ChEBI
organic chloride salts
organic chloride salt
organic chloride salts
ChEBI
A member of the class of chromenyliums that is chromene with a protonated oxygen.
chromenylium
benzopyrylium
chromenium
chromenylium
chromenylium
IUPAC
benzopyrylium
ChEBI
chromenium
ChEBI
A member of the class of chromenyliums that is chromenylium with a phenyl substituent at position 2.
flavylium
2-phenylchromenylium
flavylium
flavylium
IUPAC
2-phenylchromenylium
IUPAC
An alicyclic ketone in which the carbocyclic ring structure forms part of a terpene skeleton.
cyclic terpene ketone
cyclic terpene ketone
cyclic terpene ketone
ChEBI
A cyclic ketone in which the carbocyclic ring structure which may be saturated or unsaturated, but may not be a benzenoid or other aromatic system.
alicyclic ketone
alicyclic ketones
alicyclic ketone
alicyclic ketone
IUPAC
alicyclic ketones
IUPAC
Any alicyclic ketone that consists of a cyclopentane skeleton substituted by at least one oxo group.
cyclopentanones
Compounds having a fully conjugated cyclic dione structure, such as that of benzoquinones, derived from aromatic compounds by conversion of an even number of -CH= groups into -C(=O)- groups with any necessary rearrangement of double bonds (polycyclic and heterocyclic analogues are included).
quinone
quinones
Chinon
quinones
quinone
quinone
IUPAC
quinones
IUPAC
Chinon
ChEBI
quinones
ChEBI
A compound in which two monosaccharides are joined by a glycosidic bond.
Disaccharide
disaccharides
Disaccharid
Disacharid
disacarido
disacaridos
disaccharide
Disaccharide
KEGG_COMPOUND
disaccharides
IUPAC
Disaccharid
ChEBI
Disacharid
ChEBI
disacarido
ChEBI
disacaridos
IUPAC
A monoester of a dicarboxylic acid.
dicarboxylic acid monoesters
dicarboxylic acid monoester
dicarboxylic acid monoesters
ChEBI
macrocyclic tetrapyrroles
cyclic tetrapyrroles
macrocyclic tetrapyrrole
cyclic tetrapyrrole
macrocyclic tetrapyrroles
IUPAC
cyclic tetrapyrroles
ChEBI
macrocyclic tetrapyrrole
ChEBI
Unsaturated C18 fatty acids and skeletally related compounds.
octadecanoids
octadecanoid
octadecanoids
ChEBI
Hydroperoxy-octadecadienoic acids, formed in mammalian cells by peroxidation of linoleic acid.
HPODEs
HPODE
HPODEs
ChEBI
naphthalenesulfonic acids
naphthalenesulfonic acid
naphthalenesulfonic acids
ChEBI
Lepton is a fermion that does not experience the strong force (strong interaction). The term is derived from the Greek lambdaepsilonpitauomicronsigma (small, thin).
leptons
lepton
leptons
ChEBI
Baryon is a fermion that does experience the strong force (strong interaction). The term is derived from the Greek betaalpharhoupsilonsigma (heavy).
baryons
baryon
baryons
ChEBI
Particle of half-integer spin quantum number following Fermi-Dirac statistics. Fermions are named after Enrico Fermi.
fermion
fermions
fermion
fermion
IUPAC
fermions
ChEBI
Particle of integer spin quantum number following Bose-Einstein statistics. Bosons are named after Satyendra Nath Bose.
boson
bosons
boson
boson
IUPAC
bosons
ChEBI
A particle smaller than an atom.
subatomic particles
subatomic particle
subatomic particles
ChEBI
A subatomic particle known to have substructure (i.e. consisting of smaller particles).
composite particles
composite particle
composite particles
ChEBI
Hadron is a subatomic particle which experiences the strong force.
hadrons
hadron
hadrons
ChEBI
A nucleus or any of its constituents in any of their energy states.
nuclear particle
nuclear particle
nuclear particle
IUPAC
Any molecular entity consisting of more than one atom.
polyatomic entities
polyatomic entity
polyatomic entities
ChEBI
An ion consisting of more than one atom.
polyatomic ions
polyatomic ion
polyatomic ions
ChEBI
phosphorus oxoacid derivative
phosphorus oxoacid derivative
phosphorus oxoacid derivative
ChEBI
phosphorus oxoacids and derivatives
phosphorous acid
trihydrogen trioxophosphate(3-)
trihydroxidophosphorus
trioxophosphoric(3-) acid
H3PO3
P(OH)3
[P(OH)3]
phosphite
phosphorige Saeure
phosphorous acid
phosphorous acid
IUPAC
trihydrogen trioxophosphate(3-)
IUPAC
trihydroxidophosphorus
IUPAC
trioxophosphoric(3-) acid
IUPAC
H3PO3
IUPAC
H3PO3
NIST_Chemistry_WebBook
P(OH)3
IUPAC
[P(OH)3]
IUPAC
phosphite
UniProt
phosphorige Saeure
ChEBI
alkaline earth salts
alkaline earth salt
alkaline earth salts
ChEBI
saturated heterocyclic parent hydride
saturated heterocyclic parent hydrides
saturated organic heterocyclic parents
saturated organic heterocyclic parent
saturated heterocyclic parent hydride
ChEBI
saturated heterocyclic parent hydrides
ChEBI
saturated organic heterocyclic parents
ChEBI
saturated heteromonocyclic parent hydride
saturated heteromonocyclic parent hydrides
saturated organic heteromonocyclic parents
saturated organic heteromonocyclic parent
saturated heteromonocyclic parent hydride
ChEBI
saturated heteromonocyclic parent hydrides
ChEBI
saturated organic heteromonocyclic parents
ChEBI
mancude organic heterotricyclic parents
mancude-ring organic heterotricyclic parents
mancude organic heterotricyclic parent
mancude organic heterotricyclic parents
ChEBI
mancude-ring organic heterotricyclic parents
ChEBI
A polycyclic heteroarene that is anthracene in which one of the central CH groups is replaced by a nitrogen atom.
acridine
10-azaanthracene
2,3,5,6-dibenzopyridine
2,3-benzoquinoline
9-azaanthracene
Akridin
acrydine
benzo[b]quinoline
dibenzo[b,e]pyridine
acridine
acridine
IUPAC
10-azaanthracene
ChemIDplus
2,3,5,6-dibenzopyridine
ChemIDplus
2,3-benzoquinoline
ChemIDplus
9-azaanthracene
ChemIDplus
Akridin
NIST_Chemistry_WebBook
acrydine
NIST_Chemistry_WebBook
benzo[b]quinoline
NIST_Chemistry_WebBook
dibenzo[b,e]pyridine
NIST_Chemistry_WebBook
A C18, straight-chain, unsaturated long-chain fatty acid anion and the conjugate base of its corresponding octadecatrienoic acid, formed by deprotonation of the carboxylic acid group.
octadecatrienoate
Octadecatrienoat
octadecatrienoates
octadecatrienoate
octadecatrienoate
IUPAC
Octadecatrienoat
ChEBI
octadecatrienoates
ChEBI
pimarane
pimarane
pimarane
IUPAC
A coordination entity in which the central atom to which the ligands are attached comes from groups 1, 2, 13, 14, 15, 16, 17, or 18 of the periodic table.
main group coordination compounds
main-group coordination entities
main-group coordination entity
main group coordination compounds
ChEBI
main-group coordination entities
ChEBI
zinc group coordination compounds
zinc group coordination entities
zinc group coordination entity
zinc group coordination compounds
ChEBI
zinc group coordination entities
ChEBI
cadmium coordination compounds
cadmium coordination entities
cadmium coordination entity
cadmium coordination compounds
ChEBI
cadmium coordination entities
ChEBI
Any compound containing the carbonyl group, C=O. The term is commonly used in the restricted sense of aldehydes and ketones, although it actually includes carboxylic acids and derivatives.
carbonyl compounds
carbonyl compound
carbonyl compounds
IUPAC
Organic compounds containing an oxygen atom, =O, doubly bonded to carbon or another element.
oxo compounds
organic oxo compounds
organic oxo compound
oxo compounds
IUPAC
organic oxo compounds
ChEBI
An organochlorine compound is a compound containing at least one carbon-chlorine bond.
organochlorine compound
an organochlorine molecule
chloroorganic compounds
chlororganische Verbindungen
organochloride
organochloride compound
organochloride compounds
organochlorides
organochlorine compounds
organochlorine compound
organochlorine compound
ChEBI
an organochlorine molecule
UniProt
chloroorganic compounds
ChEBI
chlororganische Verbindungen
ChEBI
organochloride
ChEBI
organochloride compound
ChEBI
organochloride compounds
ChEBI
organochlorides
ChEBI
organochlorine compounds
ChEBI
heterotricyclic compound
heterotricyclic compounds
heterotricyclic compounds
heterotricyclic compound
heterotricyclic compound
ChEBI
heterotricyclic compounds
IUPAC
heterotricyclic compounds
ChEBI
apo carotenoid sesquiterpenoids
apocarotenoid sesquiterpenoid
apocarotenoid sesquiterpenoids
apo carotenoid sesquiterpenoid
apo carotenoid sesquiterpenoids
ChEBI
apocarotenoid sesquiterpenoid
ChEBI
apocarotenoid sesquiterpenoids
ChEBI
gibberellane
ent-gibberellane
A bicyclic compound in which all the ring atoms are carbon.
carbobicyclic compounds
carbobicyclic compound
carbobicyclic compounds
ChEBI
pseudohalide ions
pseudohalide anions
pseudohalides
pseudohalogen anion
pseudohalogen ion
pseudohalide anion
pseudohalide ions
IUPAC
pseudohalide anions
ChEBI
pseudohalides
ChEBI
pseudohalogen anion
ChEBI
pseudohalogen ion
ChEBI
polyatomic monoanions
polyatomic monoanion
polyatomic monoanions
ChEBI
monoanions
monoanion
monoanions
ChEBI
hydrogen isocyanide
nitriliomethanide
CNH
HN(+)#C(-)
HNC
hydroisocyanic acid
hydrogen isocyanide
hydrogen isocyanide
NIST_Chemistry_WebBook
nitriliomethanide
IUPAC
CNH
ChEBI
HN(+)#C(-)
IUPAC
HNC
NIST_Chemistry_WebBook
hydroisocyanic acid
ChEBI
elemental fluorine
elemental iodine
atomic fluorine
monoatomic fluorine
atomic fluorine
ChEBI
atomic iodine
monoatomic iodine
atomic iodine
ChEBI
chalcogen hydride
chalcogen hydrides
chalcogen hydride
chalcogen hydride
ChEBI
chalcogen hydrides
ChEBI
inorganic ions
inorganic ion
inorganic ions
ChEBI
inorganic cations
inorganic cation
inorganic cations
ChEBI
A monoatomic or polyatomic species having one or more elementary charges of the proton.
Cation
cation
Kation
Kationen
cationes
cations
cation
Cation
KEGG_COMPOUND
cation
ChEBI
cation
IUPAC
Kation
ChEBI
Kationen
ChEBI
cationes
ChEBI
cations
ChEBI
chalcocarbonic acid
chalcocarbonic acids
chalcocarbonic acids
chalcocarbonic acid
chalcocarbonic acid
ChEBI
chalcocarbonic acids
IUPAC
chalcocarbonic acids
ChEBI
An organochalcogen compound is a compound containing at least one carbon-chalcogen bond.
organochalcogen compound
organochalcogen compounds
organochalcogen compound
organochalcogen compound
ChEBI
organochalcogen compounds
ChEBI
An organochalcogen compound containing at least one carbon-oxygen bond.
organooxygen compound
organooxygen compounds
organooxygen compound
organooxygen compound
ChEBI
organooxygen compounds
ChEBI
amino-acid anion
amino acid anions
amino-acid anions
amino-acid anion
amino-acid anion
ChEBI
amino acid anions
ChEBI
amino-acid anions
ChEBI
A compound containing at least one carbon-bromine bond.
organobromine compound
an organobromine molecule
bromoorganic compound
organobromide
organobromide compound
organobromide compounds
organobromides
organobromine compounds
organobromine compound
organobromine compound
ChEBI
an organobromine molecule
UniProt
bromoorganic compound
ChEBI
organobromide
ChEBI
organobromide compound
ChEBI
organobromide compounds
ChEBI
organobromides
ChEBI
organobromine compounds
ChEBI
An organofluorine compound is a compound containing at least one carbon-fluorine bond.
organofluorine compound
fluoroorganic compound
fluoroorganic compounds
fluoroorganics
fluororganische Verbindungen
organofluorine compounds
organofluorine compound
organofluorine compound
ChEBI
fluoroorganic compound
ChEBI
fluoroorganic compounds
ChEBI
fluoroorganics
ChEBI
fluororganische Verbindungen
ChEBI
organofluorine compounds
ChEBI
A polysaccharide composed of glucose residues.
Glucan
glucan
glucans
glucan
Glucan
KEGG_COMPOUND
glucan
IUPAC
glucans
ChEBI
Glycans composed of a single type of monosaccharide residue. They are named by replacing the ending '-ose' of the sugar by '-an'.
homopolysaccharide
homoglycan
homopolysaccharides
homopolysaccharide
homopolysaccharide
IUPAC
homoglycan
IUPAC
homopolysaccharides
ChEBI
organic hydrides
organic hydride
organic hydrides
ChEBI
mononuclear parent hydrides
mononuclear hydride
mononuclear hydrides
mononuclear parent hydride
mononuclear parent hydrides
IUPAC
mononuclear hydride
ChEBI
mononuclear hydrides
IUPAC
elemental sodium
elemental potassium
elemental zinc
A substance administered to enhance contrast in images of the inside of the body obtained using X-rays, gamma-rays, sound waves, radio waves (MRI), or radioactive particles in order to diagnose disease.
diagnostic imaging agent
MRI contrast agent
elemental copper
Any ether in which the oxygen atom forms part of a ring.
cyclic ether
cyclic ethers
epoxy compounds
cyclic ethers
epoxy compounds
cyclic ether
cyclic ether
IUPAC
cyclic ethers
IUPAC
epoxy compounds
IUPAC
cyclic ethers
ChEBI
epoxy compounds
ChEBI
A group of heterocyclic compounds based on the pteroic acid skeleton conjugated with one or more L-glutamic acid units.
folates
folate
folates
folic acids
folates
IUPAC
folate
ChEBI
folates
ChEBI
An acid is a molecular entity capable of donating a hydron (Bronsted acid) or capable of forming a covalent bond with an electron pair (Lewis acid).
Acid
acid
Saeure
Saeuren
acide
acido
acids
acid
Acid
KEGG_COMPOUND
acid
IUPAC
Saeure
ChEBI
Saeuren
ChEBI
acide
IUPAC
acido
ChEBI
acids
ChEBI
A molecular entity consisting of two or more chemical elements.
chemical compound
heteroatomic molecular entities
heteroatomic molecular entity
chemical compound
ChEBI
heteroatomic molecular entities
ChEBI
Any heteroatomic molecular entity that is a chemical compound of halogen with other chemical elements.
halides
halide
halides
ChEBI
N-(2-chloroethyl)-N'-(6-chloro-2-methoxyacridin-9-yl)-N-ethylpropane-1,3-diamine
N-(2-chloroethyl)-N'-(6-chloro-2-methoxyacridin-9-yl)-N-ethylpropane-1,3-diamine
N-(2-chloroethyl)-N'-(6-chloro-2-methoxyacridin-9-yl)-N-ethylpropane-1,3-diamine
IUPAC
N(1),N(1)-bis(2-chloroethyl)-N(4)-(6-chloro-2-methoxyacridin-9-yl)pentane-1,4-diamine
quinacrine mustard
quinacrine mustard
N(1),N(1)-bis(2-chloroethyl)-N(4)-(6-chloro-2-methoxyacridin-9-yl)pentane-1,4-diamine
IUPAC
quinacrine mustard
ChemIDplus
Compounds having two beta-haloalkyl groups bound to a nitrogen atom, as in (X-CH2-CH2)2NR.
nitrogen mustards
nitrogen mustard compound
nitrogen mustard compounds
nitrogen mustards
nitrogen mustard
nitrogen mustards
IUPAC
nitrogen mustard compound
ChEBI
nitrogen mustard compounds
ChEBI
nitrogen mustards
ChEBI
Any olefinic compound having two double bonds from one carbon atom to two others.
allenes
R2C=C=CR2
allenes
allenes
IUPAC
R2C=C=CR2
IUPAC
(9Z)-octadec-9-ene
(Z)-9-octadecene
cis-9-octadecene
cis-octadec-9-ene
(9Z)-octadec-9-ene
IUPAC
(Z)-9-octadecene
NIST_Chemistry_WebBook
cis-9-octadecene
NIST_Chemistry_WebBook
octadec-9-ene
octadec-9-ene
octadec-9-ene
IUPAC
An alkene that is octadecane containing one double bond at unspecified position.
octadecene
octadecene
octadecene
IUPAC
An amide of a carboxylic acid, having the structure RC(=O)NR2. The term is used as a suffix in systematic name formation to denote the -C(=O)NH2 group including its carbon atom.
carboxamides
carboxamides
primary carboxamide
carboxamide
carboxamides
IUPAC
carboxamides
ChEBI
primary carboxamide
ChEBI
terpene lactones
terpene lactone
terpene lactones
ChEBI
An aldohexose that is the C-2 epimer of glucose.
manno-hexose
mannose
Man
mannose
manno-hexose
IUPAC
mannose
IUPAC
Man
JCBN
An EC 2.7.* (P-containing group transferase) inhibitor that interferes with the action of protein kinases.
protein kinase inhibitors
protein kinase inhibitor
protein kinase inhibitors
ChEBI
A straight chain alkane composed of 4 carbon atoms.
butane
E 943a
E-943a
E943a
N-BUTANE
R-600
n-Butan
n-C4H10
n-butane
butane
butane
IUPAC
butane
UniProt
E 943a
ChEBI
E-943a
ChEBI
E943a
ChEBI
N-BUTANE
PDBeChem
R-600
ChEBI
n-Butan
ChEBI
n-C4H10
NIST_Chemistry_WebBook
n-butane
NIST_Chemistry_WebBook
sulfuric acid derivative
sulfuric acid derivatives
sulfuric acid derivative
sulfuric acid derivative
ChEBI
sulfuric acid derivatives
ChEBI
A carboacyl group is a group formed by loss of at least one OH from the carboxy group of a carboxylic acid.
carboacyl groups
carboxylic acyl group
carboxylic acyl groups
carboacyl group
carboacyl groups
IUPAC
carboxylic acyl group
IUPAC
carboxylic acyl groups
IUPAC
A hormone that specifically regulates growth.
GH
Somatotropin
Wachstumshormon
growth hormones
growth hormone
GH
KEGG_COMPOUND
Somatotropin
KEGG_COMPOUND
Wachstumshormon
ChEBI
growth hormones
ChEBI
A plant growth regulator that modulates the formation of stems, leaves and flowers, as well as the development and ripening of fruit. The term includes endogenous and non-endogenous compounds (e.g. active compounds produced by bacteria on the leaf surface) as well as semi-synthetic and fully synthetic compounds.
phytohormone
phytohormones
plant growth factor
plant growth factors
plant growth hormone
plant growth hormones
plant hormones
plant hormone
phytohormone
ChEBI
phytohormones
ChEBI
plant growth factor
ChEBI
plant growth factors
ChEBI
plant growth hormone
ChEBI
plant growth hormones
ChEBI
plant hormones
ChEBI
chalcoperoxol
azacycloalkanes
azacycloalkane
azacycloalkanes
ChEBI
Farbstoff
Farbstoffe
colorante
colorantes
dyes
teinture
teintures
dye
Farbstoff
ChEBI
Farbstoffe
ChEBI
colorante
ChEBI
colorantes
ChEBI
dyes
ChEBI
teinture
ChEBI
teintures
ChEBI
carbohydrate sulfonates
carbohydrate sulfonate
carbohydrate sulfonates
ChEBI
The L-enantiomer of mannitol.
L-mannitol
L-mannitol
L-mannitol
IUPAC
A carbopolyclic compound comprising of three carbocyclic rings.
carbotricyclic compounds
carbotricyclic compound
carbotricyclic compounds
ChEBI
aminonaphthalenes
aminonaphthalene
aminonaphthalenes
ChEBI
A drug used in the treatment of malaria. Antimalarials are usually classified on the basis of their action against Plasmodia at different stages in their life cycle in the human.
antimalarials
antimalarial
antimalarials
ChEBI
A compound composed of two or more pyrrole units.
PPys
poly(pyrrole)s
polypyrroles
polypyrrole
PPys
ChEBI
poly(pyrrole)s
ChEBI
polypyrroles
ChEBI
Any organonitrogen compound containing a cyclic component with nitrogen and at least one other element as ring member atoms.
heterocyclic organonitrogen compounds
organonitrogen heterocyclic compounds
organonitrogen heterocyclic compound
heterocyclic organonitrogen compounds
ChEBI
organonitrogen heterocyclic compounds
ChEBI
Compounds based on a triazine skeleton.
triazines
Any organic heterocyclic compound containing at least one ring oxygen atom.
heterocyclic organooxygen compounds
organooxygen heterocyclic compounds
oxacycles
oxacycle
heterocyclic organooxygen compounds
ChEBI
organooxygen heterocyclic compounds
ChEBI
oxacycles
ChEBI
heterocyclic organosulfur compounds
organosulfur heterocyclic compounds
organosulfur heterocyclic compound
heterocyclic organosulfur compounds
ChEBI
organosulfur heterocyclic compounds
ChEBI
organic heterotetracyclic compounds
organic heterotetracyclic compound
organic heterotetracyclic compounds
ChEBI
organic heteropentacyclic compounds
organic heteropentacyclic compound
organic heteropentacyclic compounds
ChEBI
organic heteropolycyclic compounds
organic heteropolycyclic compound
organic heteropolycyclic compounds
ChEBI
triamino-1,3,5-triazines
triamino-1,3,5-triazine
triamino-1,3,5-triazines
ChEBI
monocyclic heteroarenes
monocyclic heteroarene
monocyclic heteroarenes
ChEBI
polycyclic heteroarenes
polycyclic heteroarene
polycyclic heteroarenes
ChEBI
Chlorophylls lacking the terpenoid side chain such as phytyl or farnesyl.
Chlorophyllid
chlorophyllides
chlorophyllide
Chlorophyllid
ChEBI
chlorophyllides
ChEBI
chlorophyllide b
Chlorophyllid b
chlorophyllide b
chlorophyllide b
JCBN
Chlorophyllid b
ChEBI
Any toxin produced by a plant.
phytotoxins
phytotoxin
phytotoxins
ChEBI
magnesium tetrapyrroles
magnesium tetrapyrrole
magnesium tetrapyrroles
ChEBI
Any of a class of heterocyclic amines having a saturated five-membered ring.
pyrrolidines
azirinopyrroloindoles
azirinopyrroloindole
azirinopyrroloindoles
ChEBI
gibberellin monocarboxylic acids
gibberellin monocarboxylic acid
gibberellin monocarboxylic acids
ChEBI
Any organic heterocyclic compound containing a benzene ring in which two of the C-H fragments have been replaced by isolobal nitrogens (the diazine parent structure).
diazines
Any drug used for its actions on cholinergic systems. Included here are agonists and antagonists, drugs that affect the life cycle of acetylcholine, and drugs that affect the survival of cholinergic neurons.
cholinergic agent
cholinergic drugs
cholinomimetic
cholinergic drug
cholinergic agent
ChEBI
cholinergic drugs
ChEBI
cholinomimetic
ChEBI
A pyrimidine carrying one or more oxo substituents.
pyrimidones
pyrimidone
pyrimidones
ChEBI
1-benzopyrans
1-benzopyran
1-benzopyrans
ChEBI
indol-3-yl carboxylic acid anions
indol-3-yl carboxylic acid anion
indol-3-yl carboxylic acid anions
ChEBI
electron-transport chain inhibitor
respiratory-chain inhibitor
An EC 1.9.3.* (oxidoreductase acting on donor heme group, oxygen as acceptor) inhibitor that interferes with the action of cytochrome c oxidase (EC 1.9.3.1).
CcO inhibitor
EC 1.9.3.1 (cytochrome c oxidase) inhibitors
EC 1.9.3.1 inhibitor
EC 1.9.3.1 inhibitors
NADH cytochrome c oxidase inhibitor
NADH cytochrome c oxidase inhibitors
Warburg's respiratory enzyme inhibitor
Warburg's respiratory enzyme inhibitors
complex IV (mitochondrial electron transport) inhibitor
complex IV (mitochondrial electron transport) inhibitors
cytochrome a3 inhibitor
cytochrome a3 inhibitors
cytochrome aa3 inhibitor
cytochrome aa3 inhibitors
cytochrome c oxidase (EC 1.9.3.1) inhibitor
cytochrome c oxidase (EC 1.9.3.1) inhibitors
cytochrome c oxidase inhibitor
cytochrome c oxidase inhibitors
cytochrome oxidase inhibitor
cytochrome oxidase inhibitors
cytochrome-c oxidase inhibitor
cytochrome-c oxidase inhibitors
ferrocytochrome c oxidase inhibitor
ferrocytochrome c oxidase inhibitors
ferrocytochrome-c:oxygen oxidoreductase inhibitor
ferrocytochrome-c:oxygen oxidoreductase inhibitors
indophenol oxidase inhibitor
indophenol oxidase inhibitors
indophenolase inhibitor
indophenolase inhibitors
mitochondrial complex IV inhibitor
mitochondrial complex IV inhibitors
mitochondrial cytochrome-c oxidase inhibitors
EC 1.9.3.1 (cytochrome c oxidase) inhibitor
CcO inhibitor
ChEBI
EC 1.9.3.1 (cytochrome c oxidase) inhibitors
ChEBI
EC 1.9.3.1 inhibitor
ChEBI
EC 1.9.3.1 inhibitors
ChEBI
NADH cytochrome c oxidase inhibitor
ChEBI
NADH cytochrome c oxidase inhibitors
ChEBI
Warburg's respiratory enzyme inhibitor
ChEBI
Warburg's respiratory enzyme inhibitors
ChEBI
complex IV (mitochondrial electron transport) inhibitor
ChEBI
complex IV (mitochondrial electron transport) inhibitors
ChEBI
cytochrome a3 inhibitor
ChEBI
cytochrome a3 inhibitors
ChEBI
cytochrome aa3 inhibitor
ChEBI
cytochrome aa3 inhibitors
ChEBI
cytochrome c oxidase (EC 1.9.3.1) inhibitor
ChEBI
cytochrome c oxidase (EC 1.9.3.1) inhibitors
ChEBI
cytochrome c oxidase inhibitor
ChEBI
cytochrome c oxidase inhibitors
ChEBI
cytochrome oxidase inhibitor
ChEBI
cytochrome oxidase inhibitors
ChEBI
cytochrome-c oxidase inhibitor
ChEBI
cytochrome-c oxidase inhibitors
ChEBI
ferrocytochrome c oxidase inhibitor
ChEBI
ferrocytochrome c oxidase inhibitors
ChEBI
ferrocytochrome-c:oxygen oxidoreductase inhibitor
ChEBI
ferrocytochrome-c:oxygen oxidoreductase inhibitors
ChEBI
indophenol oxidase inhibitor
ChEBI
indophenol oxidase inhibitors
ChEBI
indophenolase inhibitor
ChEBI
indophenolase inhibitors
ChEBI
mitochondrial complex IV inhibitor
ChEBI
mitochondrial complex IV inhibitors
ChEBI
mitochondrial cytochrome-c oxidase inhibitors
ChEBI
A specific group of isoquinoline alkaloids that occur only in higher plants and are constituents mainly of the Papaveraceae family.
benzophenanthridine alkaloids
benzophenanthridine alkaloid
benzophenanthridine alkaloids
ChEBI
benzophenanthridines
benzophenanthridine
benzophenanthridines
ChEBI
aminoalkylindoles
aminoalkylindole
aminoalkylindoles
ChEBI
Any agent that affects the transport of molecular entities across a biological membrane.
membrane transport modulators
membrane transport modulator
membrane transport modulators
ChEBI
Any hydroxyflavone carrying four hydroxy substituents.
tetrahydroxyflavone
tetrahydroxyflavones
tetrahydroxyflavone
tetrahydroxyflavone
ChEBI
tetrahydroxyflavones
ChEBI
inorganic sodium salts
inorganic sodium salt
inorganic sodium salts
ChEBI
Any dianion containing at least one carboxy group.
carboxylic acid dianion
carboxylic acid dianions
carboxylic acid dianion
carboxylic acid dianion
ChEBI
carboxylic acid dianions
ChEBI
A compound having the nitro group (-NO2) attached to a nitrogen atom.
N-nitro compounds
N-nitro compound
N-nitro compounds
IUPAC
pteroate
Pteroic acid
Pteroinsaeure
pteroic acid
Pteroic acid
ChemIDplus
Pteroinsaeure
ChEBI
pteroic acids
pteroates
A membrane transport modulator that is able to regulate intracellular calcium levels.
calcium channel modulators
calcium channel modulator
calcium channel modulators
ChEBI
RyR modulator
ryanodine receptor modulators
ryanodine-sensitive calcium channel modulator
ryanodine-sensitive calcium-release channel modulator
ryanodine receptor modulator
RyR modulator
ChEBI
ryanodine receptor modulators
ChEBI
ryanodine-sensitive calcium channel modulator
ChEBI
ryanodine-sensitive calcium-release channel modulator
ChEBI
A monocarboxylic acid anion that is the conjugate base of phenoxyacetic acid.
phenoxyacetate
phenoxyacetate
phenoxyacetate
IUPAC
Substance which produces loss of feeling or sensation.
anaesthetic
Anaesthetika
Anaesthetikum
anaesthetics
anesthetic agent
anesthetic drug
anesthetics
anaesthetic
anaesthetic
IUPAC
Anaesthetika
ChEBI
Anaesthetikum
ChEBI
anaesthetics
ChEBI
anesthetic agent
ChEBI
anesthetic drug
ChEBI
anesthetics
ChEBI
Substance that produces loss of consciousness.
general anaesthetic
Allgemeinanaesthetika
Allgemeinanaesthetikum
general anaesthetics
general anesthetics
general anaesthetic
general anaesthetic
IUPAC
Allgemeinanaesthetika
ChEBI
Allgemeinanaesthetikum
ChEBI
general anaesthetics
ChEBI
general anesthetics
ChEBI
Inhalationsanaesthetika
Inhalationsanaesthetikum
Inhalationsnarkotika
Inhalationsnarkotikum
anesthetic gases
inhalation anesthetics
inhalation anaesthetic
Inhalationsanaesthetika
ChEBI
Inhalationsanaesthetikum
ChEBI
Inhalationsnarkotika
ChEBI
Inhalationsnarkotikum
ChEBI
anesthetic gases
ChEBI
inhalation anesthetics
ChEBI
Drugs that used to treat infestations by flukes (trematodes) of the genus Schistosoma.
antischistosoma
antischistosomal drug
schistosomicide
schistosomicide drugs
schistosomicides
schistosomicide drug
antischistosoma
ChEBI
antischistosomal drug
ChEBI
schistosomicide
ChEBI
schistosomicide drugs
ChEBI
schistosomicides
ChEBI
Any alkylbenzene that is benzene substituted with one or more methyl groups.
methylbenzenes
methylbenzene
methylbenzenes
ChEBI
A monocyclic arene that is benzene substituted with one or more alkyl groups.
alkylbenzene
Alkylbenzol
alkylbenzenes
alkylbenzene
alkylbenzene
ChEBI
Alkylbenzol
ChEBI
alkylbenzenes
ChEBI
Any sulfur oxoacid derivative derived from sulfurous acid.
sulfurous acid derivative
sulfurous acid derivative
sulfurous acid derivative
ChEBI
calcium cation
calcium cations
calcium cation
calcium cation
ChEBI
calcium cations
ChEBI
calcium ion
calcium ions
calcium ion
calcium ion
ChEBI
calcium ions
ChEBI
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
Bronsted acid
Bronsted-Saeure
acide de Bronsted
donneur d'hydron
hydron donor
Bronsted acid
Bronsted acid
IUPAC
Bronsted-Saeure
ChEBI
acide de Bronsted
IUPAC
donneur d'hydron
IUPAC
hydron donor
IUPAC
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
Bronsted base
Bronsted-Base
accepteur d'hydron
base de Bronsted
hydron acceptor
Bronsted base
Bronsted base
IUPAC
Bronsted-Base
ChEBI
accepteur d'hydron
IUPAC
base de Bronsted
IUPAC
hydron acceptor
IUPAC
A molecular entity that is an electron-pair acceptor and therefore able to form a covalent bond with an electron-pair donor (Lewis base), thereby producing a Lewis adduct.
Lewis acid
Lewis-Saeure
accepteur d'une paire d'electrons
acide de Lewis
electron acceptor
electron-pair acceptor
Lewis acid
Lewis acid
IUPAC
Lewis-Saeure
ChEBI
accepteur d'une paire d'electrons
IUPAC
acide de Lewis
IUPAC
electron acceptor
ChEBI
electron-pair acceptor
IUPAC
A molecular entity able to provide a pair of electrons and thus capable of forming a covalent bond with an electron-pair acceptor (Lewis acid), thereby producing a Lewis adduct.
Lewis base
Lewis-Base
base de Lewis
donneur d'une paire d'electrons
electron donor
Lewis base
Lewis base
IUPAC
Lewis-Base
ChEBI
base de Lewis
IUPAC
donneur d'une paire d'electrons
ChEBI
electron donor
ChEBI
An N-nitro compound that is guanidine in which one of the hydrogens is replaced by a nitro group. It can exist in distinct tautomeric forms, as 1-nitroguanidine (a nitroimine) or 2-nitroguanidine (a nitroamine); in both solid and in solution, the nitroimine form predominates.
nitroguanidine
picrite
nitroguanidine
nitroguanidine
IUPAC
picrite
NIST_Chemistry_WebBook
Any organonitrogen heterocyclic compound based on a phenazine skeleton and derivatives.
phenazines
dibenzopyridines
dibenzopyridine
dibenzopyridines
ChEBI
A volatile or volatilizable chemical compound utilized for control of pests in buildings, soil, grain, as well as during processing of goods to be imported or exported to prevent transfer of exotic organisms.
fumigant pesticide
fumigants
fumigant
fumigant pesticide
ChEBI
fumigants
ChEBI
Any chemical substance that inhibits the life-cycle of an organism.
growth regulators
growth regulator
growth regulators
ChEBI
Any saturated fatty acid lacking a side-chain.
straight-chain saturated fatty acid
straight-chain saturated fatty acids
straight-chain saturated fatty acid
straight-chain saturated fatty acid
ChEBI
straight-chain saturated fatty acids
ChEBI
pyrimidine ribonucleosides
Any compound having a pyrimidine as part of its structure.
pyrimidines
Any drug which can be used to prevent or alleviate glaucoma, a disease in which the optic nerve is damaged, resulting in progressive, irreversible loss of vision. It is often, though not always, associated with increased pressure of the fluid in the eye.
anti-glaucoma agent
anti-glaucoma agents
anti-glaucoma drug
anti-glaucoma drugs
antiglaucoma agent
antiglaucoma drugs
antiglaucoma drug
anti-glaucoma agent
ChEBI
anti-glaucoma agents
ChEBI
anti-glaucoma drug
ChEBI
anti-glaucoma drugs
ChEBI
antiglaucoma agent
ChEBI
antiglaucoma drugs
ChEBI
A monovalent inorganic anion that consists of phosphoric acid in which one of the three OH groups has been deprotonated.
dihydrogen(tetraoxidophosphate)(1-)
dihydrogenphosphate
dihydrogentetraoxophosphate(1-)
dihydrogentetraoxophosphate(V)
dihydroxidodioxidophosphate(1-)
DIHYDROGENPHOSPHATE ION
H2PO4(-)
[PO2(OH)2](-)
dihydrogenphosphate
dihydrogen(tetraoxidophosphate)(1-)
IUPAC
dihydrogenphosphate
IUPAC
dihydrogentetraoxophosphate(1-)
IUPAC
dihydrogentetraoxophosphate(V)
IUPAC
dihydroxidodioxidophosphate(1-)
IUPAC
DIHYDROGENPHOSPHATE ION
PDBeChem
H2PO4(-)
IUPAC
[PO2(OH)2](-)
IUPAC
Cyclic ketone
cyclic ketones
cyclic ketone
Cyclic ketone
KEGG_COMPOUND
cyclic ketones
IUPAC
A butanediol that is butane in which one hydrogen of each of the methyl groups is substituted by a hydroxy group. A colourless, water-miscible, viscous liquid at room temperature (m.p. 16degreeC) with a high boiling point (230degreeC), it is mainly used for the production of other organic chemicals, particularly the solvent oxolane (also known as tetrahydrofuran or THF).
butane-1,4-diol
1,4-BD
1,4-BUTANEDIOL
1,4-butylene glycol
1,4-dihydroxybutane
1,4-tetramethylene glycol
HO(CH2)4OH
HOCH2CH2CH2CH2OH
tetramethylene 1,4-diol
tetramethylene glycol
butane-1,4-diol
butane-1,4-diol
IUPAC
1,4-BD
ChemIDplus
1,4-BUTANEDIOL
PDBeChem
1,4-butylene glycol
ChemIDplus
1,4-dihydroxybutane
ChemIDplus
1,4-tetramethylene glycol
ChemIDplus
HO(CH2)4OH
ChEBI
HOCH2CH2CH2CH2OH
ChEBI
tetramethylene 1,4-diol
ChemIDplus
tetramethylene glycol
ChemIDplus
CARBOXYMETHYL GROUP
carboxymethyl
-CH2-COOH
aspartic acid side-chain
carboxymethyl group
CARBOXYMETHYL GROUP
PDBeChem
carboxymethyl
IUPAC
-CH2-COOH
ChEBI
aspartic acid side-chain
ChEBI
carbonate
trioxidocarbonate(2-)
CARBONATE ION
CO3(2-)
Karbonat
[CO3](2-)
carbonate
carbonate
IUPAC
trioxidocarbonate(2-)
IUPAC
CARBONATE ION
PDBeChem
CO3(2-)
ChEBI
Karbonat
ChEBI
[CO3](2-)
IUPAC
An alkane comprising of two carbon atoms.
ETHANE
ethane
Aethan
C2H6
CH3-CH3
Ethan
R-170
bimethyl
dimethyl
ethyl hydride
methylmethane
ethane
ETHANE
PDBeChem
ethane
IUPAC
Aethan
ChEBI
C2H6
ChEBI
CH3-CH3
IUPAC
Ethan
ChEBI
R-170
ChEBI
bimethyl
NIST_Chemistry_WebBook
dimethyl
NIST_Chemistry_WebBook
ethyl hydride
NIST_Chemistry_WebBook
methylmethane
NIST_Chemistry_WebBook
FORMYL GROUP
aldehyde group
carbaldehyde
formyl
-CH(O)
-CHO
Fo
H-CO-
methanoyl
formyl group
FORMYL GROUP
PDBeChem
aldehyde group
IUPAC
carbaldehyde
IUPAC
formyl
IUPAC
-CH(O)
IUPAC
-CHO
IUPAC
Fo
CBN
H-CO-
IUPAC
methanoyl
IUPAC
An aminocarboxamidine, the parent compound of the guanidines.
GUANIDINE
guanidine
Gu
H2N-C(=NH)-NH2
aminomethanamidine
guanidin
iminourea
guanidine
GUANIDINE
PDBeChem
guanidine
IUPAC
Gu
ChEBI
H2N-C(=NH)-NH2
IUPAC
aminomethanamidine
NIST_Chemistry_WebBook
guanidin
ChEBI
iminourea
NIST_Chemistry_WebBook
HYDROXY GROUP
hydroxy
hydroxy group
-OH
hydroxyl
hydroxyl group
hydroxy group
HYDROXY GROUP
PDBeChem
hydroxy
IUPAC
hydroxy group
UniProt
-OH
IUPAC
hydroxyl
ChEBI
hydroxyl group
ChEBI
(4S)-4-hydroxy-3,4-dihydropyrimidin-2(1H)-one
A phosphate ion that is the conjugate base of dihydrogenphosphate.
hydrogen(tetraoxidophosphate)(2-)
hydrogenphosphate
hydrogentetraoxophosphate(2-)
hydrogentetraoxophosphate(V)
hydroxidotrioxidophosphate(2-)
HPO4(2-)
HYDROGENPHOSPHATE ION
INORGANIC PHOSPHATE GROUP
[P(OH)O3](2-)
[PO3(OH)](2-)
hydrogen phosphate
phosphate
hydrogenphosphate
hydrogen(tetraoxidophosphate)(2-)
IUPAC
hydrogenphosphate
IUPAC
hydrogentetraoxophosphate(2-)
IUPAC
hydrogentetraoxophosphate(V)
IUPAC
hydroxidotrioxidophosphate(2-)
IUPAC
HPO4(2-)
IUPAC
HYDROGENPHOSPHATE ION
PDBeChem
INORGANIC PHOSPHATE GROUP
PDBeChem
[P(OH)O3](2-)
MolBase
[PO3(OH)](2-)
IUPAC
hydrogen phosphate
ChEBI
phosphate
UniProt
dioxidanediide
dioxide(2-)
peroxide
O2(2-)
PEROXIDE ION
[O2](2-)
peroxide
dioxidanediide
IUPAC
dioxide(2-)
IUPAC
peroxide
IUPAC
O2(2-)
IUPAC
PEROXIDE ION
PDBeChem
[O2](2-)
ChEBI
A phosphorus oxoacid that consists of a single pentavalent phosphorus covalently bound via single bonds to a single hydrogen and two hydroxy groups and via a double bond to an oxygen. The parent of the class of phosphonic acids.
Phosphonic acid
dihydrogen hydridotrioxophosphate(2-)
hydridodihydroxidooxidophosphorus
hydridotrioxophosphoric(2-) acid
phosphonic acid
(HO)2HPO
H2PHO3
H3PO3
HPO(OH)2
Phosphite
Phosphonate
Phosphonsaeure
[PHO(OH)2]
phosphonic acid
Phosphonic acid
KEGG_COMPOUND
dihydrogen hydridotrioxophosphate(2-)
IUPAC
hydridodihydroxidooxidophosphorus
IUPAC
hydridotrioxophosphoric(2-) acid
IUPAC
phosphonic acid
ChEBI
(HO)2HPO
NIST_Chemistry_WebBook
H2PHO3
IUPAC
H3PO3
ChEBI
HPO(OH)2
IUPAC
Phosphite
KEGG_COMPOUND
Phosphonate
KEGG_COMPOUND
Phosphonsaeure
ChEBI
[PHO(OH)2]
IUPAC
A trivalent inorganic anion obtained by removal of all three protons from phosphorous acid.
trioxidophosphate(3-)
trioxophosphate(3-)
trioxophosphate(III)
PHOSPHITE ION
PO3(3-)
Phosphit
[PO3](3-)
phosphite
phosphite(3-)
trioxidophosphate(3-)
IUPAC
trioxophosphate(3-)
IUPAC
trioxophosphate(III)
IUPAC
PHOSPHITE ION
PDBeChem
PO3(3-)
IUPAC
Phosphit
ChEBI
[PO3](3-)
IUPAC
phosphite
IUPAC
hydrogen(tetraoxidosulfate)(1-)
hydrogensulfate
hydrogensulfate(1-)
hydrogentetraoxosulfate(1-)
hydrogentetraoxosulfate(VI)
hydroxidotrioxidosulfate(1-)
HSO4(-)
HYDROGEN SULFATE
[SO3(OH)](-)
hydrogensulfate
hydrogen(tetraoxidosulfate)(1-)
IUPAC
hydrogensulfate
IUPAC
hydrogensulfate(1-)
IUPAC
hydrogentetraoxosulfate(1-)
IUPAC
hydrogentetraoxosulfate(VI)
IUPAC
hydroxidotrioxidosulfate(1-)
IUPAC
HSO4(-)
IUPAC
HYDROGEN SULFATE
PDBeChem
[SO3(OH)](-)
IUPAC
OXO GROUP
oxo
=O
oxo group
OXO GROUP
PDBeChem
oxo
IUPAC
=O
IUPAC
In general, a mineral is a chemical substance that is normally crystalline formed and has been formed as a result of geological processes. The term also includes metamict substances (naturally occurring, formerly crystalline substances whose crystallinity has been destroyed by ionising radiation) and can include naturally occurring amorphous substances that have never been crystalline ('mineraloids') such as georgite and calciouranoite as well as substances formed by the action of geological processes on bigenic compounds ('biogenic minerals').
mineral
Minerale
minerales
minerals
mineraux
mineral
mineral
ChEBI
Minerale
ChEBI
minerales
ChEBI
minerals
ChEBI
mineraux
ChEBI
Any ether that contains more than one ether linkage.
polyether
polyethers
polyether
polyether
ChEBI
polyethers
ChEBI
A liquid that can dissolve other substances (solutes) without any change in their chemical composition.
Loesungsmittel
solvant
solvents
solvent
Loesungsmittel
ChEBI
solvant
ChEBI
solvents
ChEBI
Any ether carrying a hydroxy group at unspecified position.
hydroxyether
hydroxyether
hydroxyether
ChEBI
A hydroxyether that is ethanol substituted by a methoxy group at position 2.
2-METHOXYETHANOL
2-methoxyethanol
1-hydroxy-2-methoxyethane
2-hydroxyethyl methyl ether
2-methoxy-1-ethanol
3-oxa-1-butanol
HOCH2CH2OCH3
Methyl cellosolve
beta-methoxyethanol
methyl oxitol
monomethyl ethylene glycol ether
2-methoxyethanol
2-METHOXYETHANOL
PDBeChem
2-methoxyethanol
IUPAC
1-hydroxy-2-methoxyethane
ChemIDplus
2-hydroxyethyl methyl ether
NIST_Chemistry_WebBook
2-methoxy-1-ethanol
ChemIDplus
3-oxa-1-butanol
ChemIDplus
HOCH2CH2OCH3
NIST_Chemistry_WebBook
Methyl cellosolve
ChemIDplus
beta-methoxyethanol
NIST_Chemistry_WebBook
methyl oxitol
ChemIDplus
monomethyl ethylene glycol ether
ChemIDplus
A hydroxyether compound containing more than one ether group.
hydroxypolyether
hydroxypolyether
hydroxypolyether
ChEBI
A polymer composed of repeating ethyleneoxy units.
alpha-hydro-omega-hydroxypoly(oxyethylene)
1,2-ethanediol homopolymer
Glycols, polyethylene
Macrogol
PEG
PEO
POE
Polyaethylenglykol
Polyaethylenglykole
Polyethylene glycol
alpha,omega-hydroxypoly(ethylene oxide)
alpha-hydro-omega-hydroxypoly(oxy-1,2-ethanediyl)
alpha-hydro-omega-hydroxypoly(oxyethylene)
ethylene glycol homopolymer
ethylene glycol polymer
poly(ethyleneoxide)
poly(oxyethylene)
polyethylene glycol
polyethylene glycols
polyethylene oxide
polyoxyethylene
poly(ethylene glycol)
alpha-hydro-omega-hydroxypoly(oxyethylene)
IUPAC
1,2-ethanediol homopolymer
ChemIDplus
Glycols, polyethylene
ChemIDplus
Macrogol
ChemIDplus
PEG
ChEBI
PEG
ChemIDplus
PEO
SUBMITTER
POE
SUBMITTER
Polyaethylenglykol
ChEBI
Polyaethylenglykole
ChEBI
Polyethylene glycol
ChemIDplus
alpha,omega-hydroxypoly(ethylene oxide)
NIST_Chemistry_WebBook
alpha-hydro-omega-hydroxypoly(oxy-1,2-ethanediyl)
NIST_Chemistry_WebBook
alpha-hydro-omega-hydroxypoly(oxyethylene)
NIST_Chemistry_WebBook
ethylene glycol homopolymer
ChemIDplus
ethylene glycol polymer
ChemIDplus
poly(ethyleneoxide)
SUBMITTER
poly(oxyethylene)
SUBMITTER
polyethylene glycol
ChEBI
polyethylene glycols
ChEBI
polyethylene oxide
SUBMITTER
polyoxyethylene
SUBMITTER
indolyl carboxylic acids
indolyl carboxylic acid
indolyl carboxylic acids
ChEBI
CARBOXY GROUP
carboxy
-C(O)OH
-CO2H
-COOH
carboxyl group
carboxy group
CARBOXY GROUP
PDBeChem
carboxy
IUPAC
-C(O)OH
IUPAC
-CO2H
ChEBI
-COOH
IUPAC
carboxyl group
ChEBI
2,5-diammoniopentanoate
ornithinium
ornithinium(1+)
ornithine monocation
ornithinium(1+)
2,5-diammoniopentanoate
IUPAC
ornithinium
IUPAC
ornithinium(1+)
JCBN
ornithine monocation
JCBN
1-carboxybutane-1,4-diaminium
ornithinediium
ornithinium(2+)
ornithine dication
ornithinium(2+)
1-carboxybutane-1,4-diaminium
IUPAC
ornithinediium
IUPAC
ornithinium(2+)
JCBN
ornithine dication
JCBN
tetrahydrofuranols
tetrahydrofuranol
tetrahydrofuranols
ChEBI
dihydroxytetrahydrofurans
dihydroxytetrahydrofuran
dihydroxytetrahydrofurans
ChEBI
ammonium salt
Ammoniumsalz
Ammoniumsalze
ammonium salts
ammonium salt
ammonium salt
ChEBI
Ammoniumsalz
ChEBI
Ammoniumsalze
ChEBI
ammonium salts
ChEBI
Any ester resulting from the condensation of one or more of the hydroxy groups of glycerol (propane-1,2,3-triol) with fatty acids.
glyceride
glycerides
acylglycerols
glycerides
glyceride
glyceride
ChEBI
glycerides
IUPAC
acylglycerols
ChEBI
glycerides
ChEBI
aminoglycosides
aminoglycoside
aminoglycosides
ChEBI
urea derivatives
ureas
urea derivatives
ChEBI
Anything used in a scientific experiment to indicate the presence of a substance or quality, change in a body, etc.
Indikator
indicator
Indikator
ChEBI
A chemical compound that can be excited by light of a specific wavelength and subsequently transfer energy to a chosen reactant. This is commonly molecular oxygen within a cancer tissue, which is converted to (highly rective) singlet state oxygen. This rapidly reacts with any nearby biomolecules, ultimately killing the cancer cells.
photosensitising agent
photosensitizing agent
photosensitising agent
ChEBI
macrocyclic polypyrroles
cyclic polypyrroles
polypyrrole macrocycles
cyclic polypyrrole
macrocyclic polypyrroles
IUPAC
cyclic polypyrroles
ChEBI
polypyrrole macrocycles
ChEBI
Organic derivatives of sulfonic acid in which the sulfo group is linked directly to carbon of an alkyl group.
alkanesulfonic acids
alkylsulfonic acids
alkanesulfonic acid
alkanesulfonic acids
ChEBI
alkylsulfonic acids
ChEBI
Any member of the 'superclass' flavonoids whose skeleton is based on 1-benzopyran with an aryl substituent at position 2. The term was originally restricted to natural products, but is now also used to describe semi-synthetic and fully synthetic compounds.
Flavonoid
2-aryl-1-benzopyran
2-aryl-1-benzopyrans
flavonoids
flavonoid
Flavonoid
KEGG_COMPOUND
2-aryl-1-benzopyran
ChEBI
2-aryl-1-benzopyrans
ChEBI
flavonoids
ChEBI
A nitrogen oxoacid of formula HNO3 in which the nitrogen atom is bonded to a hydroxy group and by equivalent bonds to the remaining two oxygen atoms.
Nitric acid
hydrogen trioxonitrate(1-)
hydroxidodioxidonitrogen
trioxonitric acid
HNO3
HONO2
Salpetersaeure
[NO2(OH)]
acide azotique
acide nitrique
azotic acid
hydrogen nitrate
nitric acid
Nitric acid
KEGG_COMPOUND
hydrogen trioxonitrate(1-)
IUPAC
hydroxidodioxidonitrogen
IUPAC
trioxonitric acid
IUPAC
HNO3
IUPAC
HONO2
NIST_Chemistry_WebBook
Salpetersaeure
ChemIDplus
[NO2(OH)]
IUPAC
acide azotique
ChEBI
acide nitrique
ChemIDplus
azotic acid
ChemIDplus
hydrogen nitrate
NIST_Chemistry_WebBook
Schwefeloxide
oxides of sulfur
sulfur oxides
sulfur oxide
Schwefeloxide
ChEBI
oxides of sulfur
ChEBI
sulfur oxides
ChEBI
A substance used locally on humans and other animals to destroy harmful microorganisms or to inhibit their activity (cf. disinfectants, which destroy microorganisms found on non-living objects, and antibiotics, which can be transported through the lymphatic system to destroy bacteria within the body).
antiseptic
antiseptic agent
antiseptic agents
antiseptics
local antiinfective agents
local microbicides
topical antiinfective agents
topical microbicides
antiseptic drug
antiseptic
ChEBI
antiseptic agent
ChEBI
antiseptic agents
ChEBI
antiseptics
ChEBI
local antiinfective agents
ChEBI
local microbicides
ChEBI
topical antiinfective agents
ChEBI
topical microbicides
ChEBI
An antimicrobial agent that is applied to non-living objects to destroy harmful microorganisms or to inhibit their activity.
Desinfektionsmittel
desinfectant
disinfectants
disinfecting agent
disinfectant
Desinfektionsmittel
ChEBI
desinfectant
ChEBI
disinfectants
ChEBI
disinfecting agent
ChEBI
A solvent that is composed of polar molecules. Polar solvents can dissolve ionic compounds or ionisable covalent compounds.
polar solvent
polar solvents
polar solvent
polar solvent
IUPAC
polar solvents
ChEBI
non-polar solvent
A polar solvent that is capable of acting as a hydron (proton) donor.
protogenic solvent
protic solvent
protogenic solvent
IUPAC
aprotic solvent
A solvent with a comparatively high relative permittivity (or dielectric constant), greater than ca. 15, and a sizable permanent dipole moment, that cannot donate suitably labile hydrogen atoms to form strong hydrogen bonds.
dipolar aprotic solvent
polar aprotic solvent
dipolar aprotic solvent
IUPAC
Solvent that is capable of acting as a hydron (proton) acceptor.
protophilic solvent
HBA solvent
hydrogen bond acceptor solvent
protophilic solvent
protophilic solvent
IUPAC
HBA solvent
ChEBI
hydrogen bond acceptor solvent
ChEBI
Self-ionizing solvent possessing both characteristics of Bronsted acids and bases.
amphiprotic solvent
amphiprotic solvent
amphiprotic solvent
IUPAC
carbamimidic acid
H2N-C(=NH)-OH
H2N-C(OH)=NH
HO-C(=NH)-NH2
Isoharnstoff
carbamimic acid
carbonamidimidic acid
isourea
pseudourea
carbamimidic acid
carbamimidic acid
IUPAC
H2N-C(=NH)-OH
IUPAC
H2N-C(OH)=NH
IUPAC
HO-C(=NH)-NH2
IUPAC
Isoharnstoff
ChEBI
carbamimic acid
ChemIDplus
carbonamidimidic acid
IUPAC
isourea
ChemIDplus
pseudourea
ChemIDplus
Compounds derived from oxoacids RkE(=O)l(OH)m (l =/= 0) by replacing =O by =NR; thus tautomers of amides. In organic chemistry an unspecified imidic acid is generally a carboximidic acid, RC(=NR)(OH).
imidic acid
imidic acids
imidic acids
imino acids
imidic acid
imidic acid
ChEBI
imidic acids
IUPAC
imidic acids
ChEBI
imino acids
IUPAC
carboximidic acid
carboximidic acids
carboximidic acids
carboximidic acid
carboximidic acid
ChEBI
carboximidic acids
IUPAC
carboximidic acids
ChEBI
A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.
isoureas
isoureas
isourea
isoureas
IUPAC
isoureas
ChEBI
An agent and endogenous substances that antagonize or inhibit the development of new blood vessels.
angiogenesis antagonist
angiostatic agents
anti-angiogenic agent
angiogenesis inhibitor
angiogenesis antagonist
ChEBI
angiostatic agents
ChEBI
anti-angiogenic agent
ChEBI
Esters or salts of methanesulfonic acid.
methanesulfonates
A role played by a substance that can react readily with, and thereby eliminate, radicals.
free radical scavengers
free-radical scavenger
radical scavenger
free radical scavengers
ChEBI
free-radical scavenger
ChEBI
Substance which binds to cell receptors normally responding to naturally occurring substances and which produces a response of its own.
agonist
agonista
agoniste
agonists
agonist
agonist
IUPAC
agonista
ChEBI
agoniste
ChEBI
agonists
ChEBI
Substance that attaches to and blocks cell receptors that normally bind naturally occurring substances.
antagonist
antagonista
antagoniste
antagonists
antagonist
antagonist
IUPAC
antagonista
ChEBI
antagoniste
ChEBI
antagonists
ChEBI
Sulfurous acid
dihydrogen trioxosulfate
dihydroxidooxidosulfur
sulfurous acid
trioxosulfuric acid
H2SO3
S(O)(OH)2
Sulfite
[SO(OH)2]
acide sulfureux
acido sulfuroso
schweflige Saeure
sulphurous acid
sulfurous acid
Sulfurous acid
KEGG_COMPOUND
dihydrogen trioxosulfate
IUPAC
dihydroxidooxidosulfur
IUPAC
sulfurous acid
IUPAC
trioxosulfuric acid
IUPAC
H2SO3
IUPAC
S(O)(OH)2
IUPAC
Sulfite
KEGG_COMPOUND
[SO(OH)2]
IUPAC
acide sulfureux
ChEBI
acido sulfuroso
ChEBI
schweflige Saeure
ChemIDplus
sulphurous acid
ChemIDplus
sulfite salt
benzothiadiazoles
benzothiadiazole
benzothiadiazoles
ChEBI
Any drug that binds to but does not activate cholinergic receptors, thereby blocking the actions of acetylcholine or cholinergic agonists.
Anticholinergika
Anticholinergikum
acetylcholine antagonists
acetylcholine receptor antagonist
agent anticholinergique
agente anticolinergico
agentes anticolinergicos
anticholinergic agents
anticholinergics
anticholinergiques
anticolinergicos
cholinergic-blocking agents
cholinergic antagonist
Anticholinergika
ChEBI
Anticholinergikum
ChEBI
acetylcholine antagonists
ChEBI
acetylcholine receptor antagonist
IUPHAR
agent anticholinergique
ChEBI
agente anticolinergico
ChEBI
agentes anticolinergicos
ChEBI
anticholinergic agents
ChEBI
anticholinergics
ChEBI
anticholinergiques
ChEBI
anticolinergicos
ChEBI
cholinergic-blocking agents
ChEBI
Any L-alpha-amino acid carrying an N-acyl substituent.
N-Acyl-L-amino acid
N-acyl-L-alpha-amino acid
N-Acyl-L-amino acid
KEGG_COMPOUND
6beta,18-epoxy-9beta-pimara-7,15-diene-3,18-dione
momilactone A
3-oxo-9beta-pimara-7,15-dien-19,6beta-olide
Momilacton A
momilactone A
6beta,18-epoxy-9beta-pimara-7,15-diene-3,18-dione
IUPAC
momilactone A
UniProt
3-oxo-9beta-pimara-7,15-dien-19,6beta-olide
IUPAC
Momilacton A
ChemIDplus
pimarane diterpenoid
pimarane diterpenoids
pimarane diterpenoid
pimarane diterpenoid
ChEBI
pimarane diterpenoids
ChEBI
diterpene lactones
diterpene lactone
diterpene lactones
ChEBI
2-hydroxy acid
2-hydroxy monocarboxylic acids
2-hydroxy monocarboxylic acid
2-hydroxy acid
ChEBI
2-hydroxy monocarboxylic acids
ChEBI
hydrogen
1H
H
Wasserstoff
hidrogeno
hydrogen
hydrogene
hydrogen atom
hydrogen
IUPAC
1H
IUPAC
H
IUPAC
Wasserstoff
ChEBI
hidrogeno
ChEBI
hydrogen
ChEBI
hydrogene
ChEBI
A compound formally derived from ammonia by replacing one, two or three hydrogen atoms by organyl groups.
organic amino compounds
organic amino compound
organic amino compounds
ChEBI
A member of the class of N-nitrosoureas that is urea in which one of the nitrogens is substituted by methyl and nitroso groups.
1-methyl-1-nitrosourea
N-Methyl-N-nitrosourea
1-(aminocarbonyl)-1-methyl-2-oxohydrazine
1-nitroso-1-methylurea
MNU
Methylnitrosoharnstoff
Methylnitrosourea
N-Methyl-N-nitrosoharnstoff
N-Nitroso-N-methylharnstoff
N-methyl-N-nitrosocarbamide
N-methyl-N-nitrosouree
N-nitroso-N-methylcarbamide
N-nitroso-N-methylurea
N-nitroso-N-methyluree
N-nitrosomethylurea
NMH
NMU
methylnitrosouree
nitrosomethylurea
N-methyl-N-nitrosourea
1-methyl-1-nitrosourea
IUPAC
N-Methyl-N-nitrosourea
KEGG_COMPOUND
1-(aminocarbonyl)-1-methyl-2-oxohydrazine
NIST_Chemistry_WebBook
1-nitroso-1-methylurea
ChemIDplus
MNU
ChemIDplus
Methylnitrosoharnstoff
ChEBI
Methylnitrosourea
KEGG_COMPOUND
N-Methyl-N-nitrosoharnstoff
ChEBI
N-Nitroso-N-methylharnstoff
ChEBI
N-methyl-N-nitrosocarbamide
ChemIDplus
N-methyl-N-nitrosouree
ChEBI
N-nitroso-N-methylcarbamide
NIST_Chemistry_WebBook
N-nitroso-N-methylurea
ChemIDplus
N-nitroso-N-methyluree
ChEBI
N-nitrosomethylurea
NIST_Chemistry_WebBook
NMH
ChemIDplus
NMU
ChemIDplus
methylnitrosouree
ChemIDplus
nitrosomethylurea
NIST_Chemistry_WebBook
An agent that binds to and activates excitatory amino acid receptors.
excitatory amino acid agonists
excitatory amino acid receptor agonist
excitatory amino acid receptor agonists
excitatory amino acid agonist
excitatory amino acid agonists
ChEBI
excitatory amino acid receptor agonist
ChEBI
excitatory amino acid receptor agonists
ChEBI
A drug that softens, separates, and causes desquamation of the cornified epithelium or horny layer of skin. Keratolytic drugs are used to expose mycelia of infecting fungi or to treat corns, warts, and certain other skin diseases.
desquamating agent
keratolytic agent
keratolytic drugs
skin-peeling agent
keratolytic drug
desquamating agent
ChEBI
keratolytic agent
ChEBI
keratolytic drugs
ChEBI
skin-peeling agent
ChEBI
A drug used to treat or prevent skin disorders or for the routine care of skin.
dermatologic agent
dermatologic drugs
dermatological agent
dermatologic drug
dermatologic agent
ChEBI
dermatologic drugs
ChEBI
dermatological agent
ChEBI
A substance that can be converted into a vitamin by animal tissues.
provitamins
provitamin
provitamins
ChEBI
An EC 3.1.* (ester hydrolase) inhibitor that interferes with the action of a phosphoric diester hydrolase (EC 3.1.4.*).
EC 3.1.4.* (phosphoric diester hydrolase) inhibitors
phosphodiesterase inhibitor
phosphodiesterase inhibitors
phosphoric diester hydrolase (EC 3.1.4.*) inhibitor
phosphoric diester hydrolase (EC 3.1.4.*) inhibitors
phosphoric diester hydrolase inhibitor
phosphoric diester hydrolase inhibitors
EC 3.1.4.* (phosphoric diester hydrolase) inhibitor
EC 3.1.4.* (phosphoric diester hydrolase) inhibitors
ChEBI
phosphodiesterase inhibitor
ChEBI
phosphodiesterase inhibitors
ChEBI
phosphoric diester hydrolase (EC 3.1.4.*) inhibitor
ChEBI
phosphoric diester hydrolase (EC 3.1.4.*) inhibitors
ChEBI
phosphoric diester hydrolase inhibitor
ChEBI
phosphoric diester hydrolase inhibitors
ChEBI
Any protective agent counteracting or neutralizing the action of poisons.
antidotes
antidote
antidotes
ChEBI
A compound that, on administration, must undergo chemical conversion by metabolic processes before becoming the pharmacologically active drug for which it is a prodrug.
Prodrugs
prodrug
Prodrugs
ChEBI
Synthetic or natural substance which is given to prevent a disease or disorder or are used in the process of treating a disease or injury due to a poisonous agent.
chemoprotectant
chemoprotectants
chemoprotective agent
chemoprotective agents
protective agents
protective agent
chemoprotectant
ChEBI
chemoprotectants
ChEBI
chemoprotective agent
ChEBI
chemoprotective agents
ChEBI
protective agents
ChEBI
A topoisomerase inhibitor that inhibits the bacterial enzymes of the DNA topoisomerases, Type I class (EC 5.99.1.2) that catalyze ATP-independent breakage of one of the two strands of DNA, passage of the unbroken strand through the break, and rejoining of the broken strand. These bacterial enzymes reduce the topological stress in the DNA structure by relaxing negatively, but not positively, supercoiled DNA.
DNA topoisomerase inhibitor
DNA topoisomerase inhibitors
EC 5.99.1.2 (DNA topoisomerase) inhibitors
EC 5.99.1.2 (topoisomerase I) inhibitor
EC 5.99.1.2 (topoisomerase I) inhibitors
EC 5.99.1.2 inhibitor
EC 5.99.1.2 inhibitors
topoisomerase I (EC 5.99.1.2) inhibitor
topoisomerase I (EC 5.99.1.2) inhibitors
topoisomerase I inhibitor
topoisomerase I inhibitors
type I DNA topoisomerase inhibitor
type I DNA topoisomerase inhibitors
EC 5.99.1.2 (DNA topoisomerase) inhibitor
DNA topoisomerase inhibitor
ChEBI
DNA topoisomerase inhibitors
ChEBI
EC 5.99.1.2 (DNA topoisomerase) inhibitors
ChEBI
EC 5.99.1.2 (topoisomerase I) inhibitor
ChEBI
EC 5.99.1.2 (topoisomerase I) inhibitors
ChEBI
EC 5.99.1.2 inhibitor
ChEBI
EC 5.99.1.2 inhibitors
ChEBI
topoisomerase I (EC 5.99.1.2) inhibitor
ChEBI
topoisomerase I (EC 5.99.1.2) inhibitors
ChEBI
topoisomerase I inhibitor
ChEBI
topoisomerase I inhibitors
ChEBI
type I DNA topoisomerase inhibitor
ChEBI
type I DNA topoisomerase inhibitors
ChEBI
canonical nucleotide residues
canonical nucleotide residue
canonical nucleotide residues
ChEBI
canonical deoxyribonucleotide residues
canonical deoxyribonucleotide residue
canonical deoxyribonucleotide residues
ChEBI
onium compound
Mononuclear cations derived by addition of a hydron to a mononuclear parent hydride of the pnictogen, chalcogen and halogen families.
onium cations
onium cations
onium ion
onium ions
onium cation
onium cations
IUPAC
onium cations
ChEBI
onium ion
ChEBI
onium ions
ChEBI
fluoranium
fluoronium
H2F(+)
[FH2](+)
fluoronium
fluoranium
IUPAC
fluoronium
IUPAC
H2F(+)
IUPAC
[FH2](+)
ChEBI
chloranium
chloronium
H2Cl(+)
[ClH2](+)
chloronium
chloranium
IUPAC
chloronium
IUPAC
H2Cl(+)
IUPAC
[ClH2](+)
IUPAC
nucleotide residues
nucleotide residue
nucleotide residues
ChEBI
nucleoside residues
nucleoside residue
nucleoside residues
ChEBI
A univalent organyl group obtained by cleaving the bond from C-2 to the side chain of a proteinogenic amino-acid.
canonical amino-acid side-chain
canonical amino-acid side-chains
proteinogenic amino-acid side-chain
proteinogenic amino-acid side-chain groups
proteinogenic amino-acid side-chains
proteinogenic amino-acid side-chain group
canonical amino-acid side-chain
ChEBI
canonical amino-acid side-chains
ChEBI
proteinogenic amino-acid side-chain
ChEBI
proteinogenic amino-acid side-chain groups
ChEBI
proteinogenic amino-acid side-chains
ChEBI
sulfanylmethyl
-CH2-SH
HS-CH2-
cysteine side-chain
sulfanylmethyl group
sulfanylmethyl
IUPAC
-CH2-SH
IUPAC
HS-CH2-
IUPAC
cysteine side-chain
ChEBI
2-carboxyethyl
glutamic acid side-chain
2-carboxyethyl group
2-carboxyethyl
IUPAC
glutamic acid side-chain
ChEBI
3-amino-3-oxopropyl
glutamine side-chain
3-amino-3-oxopropyl group
3-amino-3-oxopropyl
IUPAC
glutamine side-chain
ChEBI
1H-indol-3-ylmethyl
tryptophan side-chain
1H-indol-3-ylmethyl group
1H-indol-3-ylmethyl
IUPAC
tryptophan side-chain
ChEBI
3-carbamimidamidopropyl
3-(carbamimidoylamino)propyl
3-guanidinopropyl
arginine side-chain
3-carbamimidamidopropyl group
3-carbamimidamidopropyl
IUPAC
3-(carbamimidoylamino)propyl
IUPAC
3-guanidinopropyl
ChEBI
arginine side-chain
ChEBI
Compound that increase urine volume by increasing the amount of osmotically active solute in the urine. It also increases the osmolarity of plasma.
osmotic diuretic
Substance that sweeten food, beverages, medications, etc.
sweetener
sweeteners
sweetening agent
sweetener
ChEBI
sweeteners
ChEBI
An aliphatic alcohol in which the aliphatic alkane chain is substituted by a hydroxy group at unspecified position.
alkyl alcohols
hydroxyalkane
hydroxyalkanes
alkyl alcohol
alkyl alcohols
ChEBI
hydroxyalkane
ChEBI
hydroxyalkanes
ChEBI
An EC 1.5.1.* (oxidoreductase acting on donor CH-NH group, NAD(+) or NADP(+) as acceptor) inhibitor that interferes with the action of dihydrofolate reductase (EC 1.5.1.3).
7,8-dihydrofolate reductase inhibitor
7,8-dihydrofolate reductase inhibitors
DHFR inhibitor
DHFR inhibitors
EC 1.5.1.3 (dihydrofolate reductase) inhibitors
EC 1.5.1.3 inhibitor
EC 1.5.1.3 inhibitors
NADPH-dihydrofolate reductase inhibitor
NADPH-dihydrofolate reductase inhibitors
dihydrofolate reductase (EC 1.5.1.3) inhibitor
dihydrofolate reductase (EC 1.5.1.3) inhibitors
dihydrofolate reductase inhibitor
dihydrofolate reductase inhibitors
dihydrofolic acid reductase inhibitor
dihydrofolic acid reductase inhibitors
dihydrofolic reductase inhibitor
dihydrofolic reductase inhibitors
folic acid reductase inhibitor
folic acid reductase inhibitors
folic reductase inhibitor
folic reductase inhibitors
tetrahydrofolate dehydrogenase inhibitor
tetrahydrofolate dehydrogenase inhibitors
EC 1.5.1.3 (dihydrofolate reductase) inhibitor
7,8-dihydrofolate reductase inhibitor
ChEBI
7,8-dihydrofolate reductase inhibitors
ChEBI
DHFR inhibitor
ChEBI
DHFR inhibitors
ChEBI
EC 1.5.1.3 (dihydrofolate reductase) inhibitors
ChEBI
EC 1.5.1.3 inhibitor
ChEBI
EC 1.5.1.3 inhibitors
ChEBI
NADPH-dihydrofolate reductase inhibitor
ChEBI
NADPH-dihydrofolate reductase inhibitors
ChEBI
dihydrofolate reductase (EC 1.5.1.3) inhibitor
ChEBI
dihydrofolate reductase (EC 1.5.1.3) inhibitors
ChEBI
dihydrofolate reductase inhibitor
ChEBI
dihydrofolate reductase inhibitors
ChEBI
dihydrofolic acid reductase inhibitor
ChEBI
dihydrofolic acid reductase inhibitors
ChEBI
dihydrofolic reductase inhibitor
ChEBI
dihydrofolic reductase inhibitors
ChEBI
folic acid reductase inhibitor
ChEBI
folic acid reductase inhibitors
ChEBI
folic reductase inhibitor
ChEBI
folic reductase inhibitors
ChEBI
tetrahydrofolate dehydrogenase inhibitor
ChEBI
tetrahydrofolate dehydrogenase inhibitors
ChEBI
A reagent with two reactive groups, usually at opposite ends of the molecule, that are capable of reacting with and thereby forming bridges between macromolecules, principally side chains of amino acids in proteins, allowing the locations of naturally reactive areas within the proteins to be identified.
cross-linking reagents
cross-linking reagent
cross-linking reagents
ChEBI
A compound in which monosaccharide units are joined by glycosidic linkages. The term is commonly used to refer to a defined structure as opposed to a polymer of unspecified length or a homologous mixture. When the linkages are of other types the compounds are regarded as oligosaccharide analogues.
Oligosaccharide
oligosaccharides
O-glycosylglycoside
O-glycosylglycosides
oligosacarido
oligosacaridos
oligosaccharide
Oligosaccharide
KEGG_COMPOUND
oligosaccharides
IUPAC
O-glycosylglycoside
ChEBI
O-glycosylglycosides
ChEBI
oligosacarido
ChEBI
oligosacaridos
IUPAC
A product in capsule, tablet or liquid form that provide essential nutrients, such as a vitamin, an essential mineral, a protein, an herb, or similar nutritional substance.
Dietary Supplement
Food Supplementation
Nutritional supplement
nutraceutical
Dietary Supplement
ChEBI
Food Supplementation
ChEBI
Nutritional supplement
ChEBI
A topoisomerase inhibitor that inhibits DNA topoisomerase (ATP-hydrolysing), EC 5.99.1.3 (also known as topoisomerase II and as DNA gyrase), which catalyses ATP-dependent breakage of both strands of DNA, passage of the unbroken strands through the breaks, and rejoining of the broken strands.
DNA gyrase inhibitor
DNA gyrase inhibitors
DNA topoisomerase (ATP-hydrolysing) (EC 5.99.1.3) inhibitor
DNA topoisomerase (ATP-hydrolysing) (EC 5.99.1.3) inhibitors
DNA topoisomerase (ATP-hydrolysing) inhibitor
DNA topoisomerase (ATP-hydrolysing) inhibitors
DNA topoisomerase II inhibitor
DNA topoisomerase II inhibitors
EC 5.99.1.3 (DNA topoisomerase (ATP-hydrolysing)) inhibitor
EC 5.99.1.3 (DNA topoisomerase (ATP-hydrolysing)) inhibitors
EC 5.99.1.3 [DNA topoisomerase (ATP-hydrolysing)] inhibitors
EC 5.99.1.3 inhibitor
EC 5.99.1.3 inhibitors
inhibitor of type II topoisomerase
inhibitors of type II topoisomerase
topoisomerase II inhibitor
topoisomerase II inhibitors
topoisomerase-II inhibitor
topoisomerase-II inhibitors
type II DNA topoisomerase inhibitor
type II DNA topoisomerase inhibitors
EC 5.99.1.3 [DNA topoisomerase (ATP-hydrolysing)] inhibitor
DNA gyrase inhibitor
ChEBI
DNA gyrase inhibitors
ChEBI
DNA topoisomerase (ATP-hydrolysing) (EC 5.99.1.3) inhibitor
ChEBI
DNA topoisomerase (ATP-hydrolysing) (EC 5.99.1.3) inhibitors
ChEBI
DNA topoisomerase (ATP-hydrolysing) inhibitor
ChEBI
DNA topoisomerase (ATP-hydrolysing) inhibitors
ChEBI
DNA topoisomerase II inhibitor
ChEBI
DNA topoisomerase II inhibitors
ChEBI
EC 5.99.1.3 (DNA topoisomerase (ATP-hydrolysing)) inhibitor
ChEBI
EC 5.99.1.3 (DNA topoisomerase (ATP-hydrolysing)) inhibitors
ChEBI
EC 5.99.1.3 [DNA topoisomerase (ATP-hydrolysing)] inhibitors
ChEBI
EC 5.99.1.3 inhibitor
ChEBI
EC 5.99.1.3 inhibitors
ChEBI
inhibitor of type II topoisomerase
ChEBI
inhibitors of type II topoisomerase
ChEBI
topoisomerase II inhibitor
ChEBI
topoisomerase II inhibitors
ChEBI
topoisomerase-II inhibitor
ChEBI
topoisomerase-II inhibitors
ChEBI
type II DNA topoisomerase inhibitor
ChEBI
type II DNA topoisomerase inhibitors
ChEBI
Biologically active substance whose activity affects or plays a role in the functioning of the immune system.
Biomodulator
Immune factor
Immunologic factor
Immunological factor
immunomodulators
immunomodulator
Biomodulator
ChEBI
Immune factor
ChEBI
Immunologic factor
ChEBI
Immunological factor
ChEBI
immunomodulators
ChEBI
Any molecular entity that contains carbon.
organic compounds
organic entity
organic molecular entities
organic molecular entity
organic compounds
ChEBI
organic entity
ChEBI
organic molecular entities
ChEBI
azaarenes
azaarene
azaarenes
ChEBI
A role played by a chemical compound to induce direct or indirect DNA damage. Such damage can potentially lead to the formation of a malignant tumour, but DNA damage does not lead inevitably to the creation of cancerous cells.
genotoxic agent
genotoxic agents
genotoxins
genotoxin
genotoxic agent
ChEBI
genotoxic agents
ChEBI
genotoxins
ChEBI
A role played by a chemical compound which is known to induce a process of carcinogenesis by corrupting normal cellular pathways, leading to the acquistion of tumoral capabilities.
agente carcinogeno
cancerigene
cancerogene
carcinogen
carcinogene
carcinogenic agents
carcinogeno
carcinogens
carcinogenic agent
agente carcinogeno
ChEBI
cancerigene
ChEBI
cancerogene
ChEBI
carcinogen
ChEBI
carcinogene
ChEBI
carcinogenic agents
ChEBI
carcinogeno
ChEBI
carcinogens
ChEBI
A chemical compound, or part thereof, which causes the onset of an allergic reaction by interacting with any of the molecular pathways involved in an allergy.
alergeno
allergene
allergenic agent
allergen
alergeno
ChEBI
allergene
ChEBI
allergenic agent
ChEBI
A role played by a chemical compound in biological systems with adverse consequences in embryo developments, leading to birth defects, embryo death or altered development, growth retardation and functional defect.
agent teratogene
teratogen
teratogeno
teratogenic agent
agent teratogene
ChEBI
teratogen
ChEBI
teratogeno
ChEBI
A role is particular behaviour which a material entity may exhibit.
role
A role played by a chemical compound exihibiting itself through the ability to induce damage to the liver in animals.
agente hepatotoxico
hepatotoxic agents
hepatotoxicant
hepatotoxicants
hepatotoxin
hepatotoxins
hepatoxic agent
hepatoxicant
hepatotoxic agent
agente hepatotoxico
ChEBI
hepatotoxic agents
ChEBI
hepatotoxicant
ChEBI
hepatotoxicants
ChEBI
hepatotoxin
ChEBI
hepatotoxins
ChEBI
hepatoxic agent
ChEBI
hepatoxicant
ChEBI
A role played by a chemical compound exihibiting itself through the ability to induce damage to the kidney in animals.
agente nefrotoxico
nephrotoxicant
nephrotoxic agent
agente nefrotoxico
ChEBI
nephrotoxicant
ChEBI
A poison that interferes with the functions of the nervous system.
agente neurotoxico
nerve poison
nerve poisons
neurotoxic agent
neurotoxic agents
neurotoxicant
neurotoxins
neurotoxin
agente neurotoxico
ChEBI
nerve poison
ChEBI
nerve poisons
ChEBI
neurotoxic agent
ChEBI
neurotoxic agents
ChEBI
neurotoxicant
ChEBI
neurotoxins
ChEBI
An EC 2.7.11.* (protein-serine/threonine kinase) inhibitor that interferes with the action of non-specific serine/threonine protein kinase (EC 2.7.11.1), a kinase enzyme involved in phosphorylation of hydroxy group of serine or threonine.
A-kinase inhibitor
A-kinase inhibitors
AP50 kinase inhibitor
AP50 kinase inhibitors
ATP-protein transphosphorylase inhibitor
ATP-protein transphosphorylase inhibitors
ATP:protein phosphotransferase (non-specific) inhibitor
ATP:protein phosphotransferase (non-specific) inhibitors
BR serine/threonine-protein kinase 2 inhibitor
BR serine/threonine-protein kinase 2 inhibitors
CK-2 inhibitor
CK-2 inhibitors
CKI inhibitor
CKI inhibitors
CKII inhibitor
CKII inhibitors
EC 2.7.11.1 (non-specific serine/threonine protein kinase) inhibitors
EC 2.7.11.1 inhibitor
EC 2.7.11.1 inhibitors
HIPK2 inhibitor
HIPK2 inhibitors
Hpr kinase inhibitor
Hpr kinase inhibitors
M phase-specific cdc2 kinase inhibitor
M phase-specific cdc2 kinase inhibitors
MKNK2 inhibitor
MKNK2 inhibitors
PAK-1 inhibitor
PAK-1 inhibitors
PAK1 inhibitor
PAK1 inhibitors
PKA inhibitor
PKA inhibitors
Prp4 protein kinase inhibitor
Prp4 protein kinase inhibitors
Raf kinase inhibitor
Raf kinase inhibitors
Raf-1 inhibitor
Raf-1 inhibitors
STK32 inhibitor
STK32 inhibitors
T-antigen kinase inhibitor
T-antigen kinase inhibitors
WEE1Hu inhibitor
WEE1Hu inhibitors
Wee 1-like kinase inhibitor
Wee 1-like kinase inhibitors
Wee-kinase inhibitor
Wee-kinase inhibitors
betaIIPKC inhibitor
betaIIPKC inhibitors
cAMP-dependent protein kinase A inhibitor
cAMP-dependent protein kinase A inhibitors
cAMP-dependent protein kinase inhibitor
cAMP-dependent protein kinase inhibitors
cGMP-dependent protein kinase inhibitor
cGMP-dependent protein kinase inhibitors
calcium-dependent protein kinase C inhibitor
calcium-dependent protein kinase C inhibitors
calcium/phospholipid-dependent protein kinase inhibitor
calcium/phospholipid-dependent protein kinase inhibitors
casein kinase (phosphorylating) inhibitor
casein kinase (phosphorylating) inhibitors
casein kinase 2 inhibitor
casein kinase 2 inhibitors
casein kinase I inhibitor
casein kinase I inhibitors
casein kinase II inhibitor
casein kinase II inhibitors
casein kinase inhibitor
casein kinase inhibitors
cyclic AMP-dependent protein kinase A inhibitor
cyclic AMP-dependent protein kinase A inhibitors
cyclic AMP-dependent protein kinase inhibitor
cyclic AMP-dependent protein kinase inhibitors
cyclic monophosphate-dependent protein kinase inhibitor
cyclic monophosphate-dependent protein kinase inhibitors
cyclic nucleotide-dependent protein kinase inhibitor
cyclic nucleotide-dependent protein kinase inhibitors
cyclin-dependent kinase inhibitor
cyclin-dependent kinase inhibitors
dsk1 inhibitor
dsk1 inhibitors
epsilon PKC inhibitor
epsilon PKC inhibitors
glycogen synthase a kinase inhibitor
glycogen synthase a kinase inhibitors
glycogen synthase kinase inhibitor
glycogen synthase kinase inhibitors
hydroxyalkyl-protein kinase inhibitor
hydroxyalkyl-protein kinase inhibitors
mitogen-activated S6 kinase inhibitor
mitogen-activated S6 kinase inhibitors
non-specific serine/threonine protein kinase (EC 2.7.11.1) inhibitor
non-specific serine/threonine protein kinase (EC 2.7.11.1) inhibitors
non-specific serine/threonine protein kinase inhibitor
non-specific serine/threonine protein kinase inhibitors
p21 activated kinase-1 inhibitor
p21 activated kinase-1 inhibitors
p82 kinase inhibitor
p82 kinase inhibitors
phosphorylase b kinase kinase inhibitor
phosphorylase b kinase kinase inhibitors
protein glutamyl kinase inhibitor
protein glutamyl kinase inhibitors
protein kinase (phosphorylating) inhibitor
protein kinase (phosphorylating) inhibitors
protein kinase A inhibitor
protein kinase A inhibitors
protein kinase CK2 inhibitor
protein kinase CK2 inhibitors
protein kinase p58 inhibitor
protein kinase p58 inhibitors
protein phosphokinase inhibitor
protein phosphokinase inhibitors
protein serine kinase inhibitor
protein serine kinase inhibitors
protein serine-threonine kinase inhibitor
protein serine-threonine kinase inhibitors
protein-aspartyl kinase inhibitor
protein-aspartyl kinase inhibitors
protein-cysteine kinase inhibitor
protein-cysteine kinase inhibitors
protein-serine kinase inhibitor
protein-serine kinase inhibitors
protein-serine/threonine kinase inhibitors
ribosomal S6 protein kinase inhibitor
ribosomal S6 protein kinase inhibitors
ribosomal protein S6 kinase II inhibitor
ribosomal protein S6 kinase II inhibitors
serine kinase inhibitor
serine kinase inhibitors
serine protein kinase inhibitor
serine protein kinase inhibitors
serine(threonine) protein kinase inhibitor
serine(threonine) protein kinase inhibitors
serine-specific protein kinase inhibitor
serine-specific protein kinase inhibitors
serine/threonine protein kinase inhibitor
serine/threonine protein kinase inhibitors
threonine-specific protein kinase inhibitor
threonine-specific protein kinase inhibitors
twitchin kinase inhibitor
twitchin kinase inhibitors
type-2 casein kinase inhibitor
type-2 casein kinase inhibitors
EC 2.7.11.1 (non-specific serine/threonine protein kinase) inhibitor
A-kinase inhibitor
ChEBI
A-kinase inhibitors
ChEBI
AP50 kinase inhibitor
ChEBI
AP50 kinase inhibitors
ChEBI
ATP-protein transphosphorylase inhibitor
ChEBI
ATP-protein transphosphorylase inhibitors
ChEBI
ATP:protein phosphotransferase (non-specific) inhibitor
ChEBI
ATP:protein phosphotransferase (non-specific) inhibitors
ChEBI
BR serine/threonine-protein kinase 2 inhibitor
ChEBI
BR serine/threonine-protein kinase 2 inhibitors
ChEBI
CK-2 inhibitor
ChEBI
CK-2 inhibitors
ChEBI
CKI inhibitor
ChEBI
CKI inhibitors
ChEBI
CKII inhibitor
ChEBI
CKII inhibitors
ChEBI
EC 2.7.11.1 (non-specific serine/threonine protein kinase) inhibitors
ChEBI
EC 2.7.11.1 inhibitor
ChEBI
EC 2.7.11.1 inhibitors
ChEBI
HIPK2 inhibitor
ChEBI
HIPK2 inhibitors
ChEBI
Hpr kinase inhibitor
ChEBI
Hpr kinase inhibitors
ChEBI
M phase-specific cdc2 kinase inhibitor
ChEBI
M phase-specific cdc2 kinase inhibitors
ChEBI
MKNK2 inhibitor
ChEBI
MKNK2 inhibitors
ChEBI
PAK-1 inhibitor
ChEBI
PAK-1 inhibitors
ChEBI
PAK1 inhibitor
ChEBI
PAK1 inhibitors
ChEBI
PKA inhibitor
ChEBI
PKA inhibitors
ChEBI
Prp4 protein kinase inhibitor
ChEBI
Prp4 protein kinase inhibitors
ChEBI
Raf kinase inhibitor
ChEBI
Raf kinase inhibitors
ChEBI
Raf-1 inhibitor
ChEBI
Raf-1 inhibitors
ChEBI
STK32 inhibitor
ChEBI
STK32 inhibitors
ChEBI
T-antigen kinase inhibitor
ChEBI
T-antigen kinase inhibitors
ChEBI
WEE1Hu inhibitor
ChEBI
WEE1Hu inhibitors
ChEBI
Wee 1-like kinase inhibitor
ChEBI
Wee 1-like kinase inhibitors
ChEBI
Wee-kinase inhibitor
ChEBI
Wee-kinase inhibitors
ChEBI
betaIIPKC inhibitor
ChEBI
betaIIPKC inhibitors
ChEBI
cAMP-dependent protein kinase A inhibitor
ChEBI
cAMP-dependent protein kinase A inhibitors
ChEBI
cAMP-dependent protein kinase inhibitor
ChEBI
cAMP-dependent protein kinase inhibitors
ChEBI
cGMP-dependent protein kinase inhibitor
ChEBI
cGMP-dependent protein kinase inhibitors
ChEBI
calcium-dependent protein kinase C inhibitor
ChEBI
calcium-dependent protein kinase C inhibitors
ChEBI
calcium/phospholipid-dependent protein kinase inhibitor
ChEBI
calcium/phospholipid-dependent protein kinase inhibitors
ChEBI
casein kinase (phosphorylating) inhibitor
ChEBI
casein kinase (phosphorylating) inhibitors
ChEBI
casein kinase 2 inhibitor
ChEBI
casein kinase 2 inhibitors
ChEBI
casein kinase I inhibitor
ChEBI
casein kinase I inhibitors
ChEBI
casein kinase II inhibitor
ChEBI
casein kinase II inhibitors
ChEBI
casein kinase inhibitor
ChEBI
casein kinase inhibitors
ChEBI
cyclic AMP-dependent protein kinase A inhibitor
ChEBI
cyclic AMP-dependent protein kinase A inhibitors
ChEBI
cyclic AMP-dependent protein kinase inhibitor
ChEBI
cyclic AMP-dependent protein kinase inhibitors
ChEBI
cyclic monophosphate-dependent protein kinase inhibitor
ChEBI
cyclic monophosphate-dependent protein kinase inhibitors
ChEBI
cyclic nucleotide-dependent protein kinase inhibitor
ChEBI
cyclic nucleotide-dependent protein kinase inhibitors
ChEBI
cyclin-dependent kinase inhibitor
ChEBI
cyclin-dependent kinase inhibitors
ChEBI
dsk1 inhibitor
ChEBI
dsk1 inhibitors
ChEBI
epsilon PKC inhibitor
ChEBI
epsilon PKC inhibitors
ChEBI
glycogen synthase a kinase inhibitor
ChEBI
glycogen synthase a kinase inhibitors
ChEBI
glycogen synthase kinase inhibitor
ChEBI
glycogen synthase kinase inhibitors
ChEBI
hydroxyalkyl-protein kinase inhibitor
ChEBI
hydroxyalkyl-protein kinase inhibitors
ChEBI
mitogen-activated S6 kinase inhibitor
ChEBI
mitogen-activated S6 kinase inhibitors
ChEBI
non-specific serine/threonine protein kinase (EC 2.7.11.1) inhibitor
ChEBI
non-specific serine/threonine protein kinase (EC 2.7.11.1) inhibitors
ChEBI
non-specific serine/threonine protein kinase inhibitor
ChEBI
non-specific serine/threonine protein kinase inhibitors
ChEBI
p21 activated kinase-1 inhibitor
ChEBI
p21 activated kinase-1 inhibitors
ChEBI
p82 kinase inhibitor
ChEBI
p82 kinase inhibitors
ChEBI
phosphorylase b kinase kinase inhibitor
ChEBI
phosphorylase b kinase kinase inhibitors
ChEBI
protein glutamyl kinase inhibitor
ChEBI
protein glutamyl kinase inhibitors
ChEBI
protein kinase (phosphorylating) inhibitor
ChEBI
protein kinase (phosphorylating) inhibitors
ChEBI
protein kinase A inhibitor
ChEBI
protein kinase A inhibitors
ChEBI
protein kinase CK2 inhibitor
ChEBI
protein kinase CK2 inhibitors
ChEBI
protein kinase p58 inhibitor
ChEBI
protein kinase p58 inhibitors
ChEBI
protein phosphokinase inhibitor
ChEBI
protein phosphokinase inhibitors
ChEBI
protein serine kinase inhibitor
ChEBI
protein serine kinase inhibitors
ChEBI
protein serine-threonine kinase inhibitor
ChEBI
protein serine-threonine kinase inhibitors
ChEBI
protein-aspartyl kinase inhibitor
ChEBI
protein-aspartyl kinase inhibitors
ChEBI
protein-cysteine kinase inhibitor
ChEBI
protein-cysteine kinase inhibitors
ChEBI
protein-serine kinase inhibitor
ChEBI
protein-serine kinase inhibitors
ChEBI
protein-serine/threonine kinase inhibitors
ChEBI
ribosomal S6 protein kinase inhibitor
ChEBI
ribosomal S6 protein kinase inhibitors
ChEBI
ribosomal protein S6 kinase II inhibitor
ChEBI
ribosomal protein S6 kinase II inhibitors
ChEBI
serine kinase inhibitor
ChEBI
serine kinase inhibitors
ChEBI
serine protein kinase inhibitor
ChEBI
serine protein kinase inhibitors
ChEBI
serine(threonine) protein kinase inhibitor
ChEBI
serine(threonine) protein kinase inhibitors
ChEBI
serine-specific protein kinase inhibitor
ChEBI
serine-specific protein kinase inhibitors
ChEBI
serine/threonine protein kinase inhibitor
ChEBI
serine/threonine protein kinase inhibitors
ChEBI
threonine-specific protein kinase inhibitor
ChEBI
threonine-specific protein kinase inhibitors
ChEBI
twitchin kinase inhibitor
ChEBI
twitchin kinase inhibitors
ChEBI
type-2 casein kinase inhibitor
ChEBI
type-2 casein kinase inhibitors
ChEBI
aziridinium
aziridinium ion
aziridinium
aziridinium
IUPAC
aziridinium ion
ChEBI
Thioxanthene and its substitution derivatives.
thioxanthenes
Compounds containing an aziridine ring that contains a quaternary nitrogen atom.
aziridinium ions
aziridinium ion
aziridinium ions
ChEBI
A compound formally derived from ammonia by replacing three hydrogen atoms by organyl groups.
tertiary amino compounds
tertiary amino compound
tertiary amino compounds
ChEBI
A thioxanthen-9-one compound having a methyl substituent at the 1-position and a 2-[(diethylamino)ethyl]amino substituent at the 4-position. Formerly used for the treatment of schistosomiasis. It is a prodrug, being metabolised to hycanthone.
1-{[2-(diethylamino)ethyl]amino}-4-methyl-9H-thioxanthen-9-one
Lucanthone
1-((2-(diethylamino)ethyl)amino)-4-methylthioxanthen-9-one
1-diethylaminoethylethylamino-4-methyl-thioxanthenone
1-{[2-(diethylamino)ethyl]amino}-4-methylthioxanthen-9-one
lucanthone
lucanthonum
lucantona
lucanthone
1-{[2-(diethylamino)ethyl]amino}-4-methyl-9H-thioxanthen-9-one
IUPAC
Lucanthone
KEGG_COMPOUND
1-((2-(diethylamino)ethyl)amino)-4-methylthioxanthen-9-one
ChemIDplus
1-diethylaminoethylethylamino-4-methyl-thioxanthenone
ChEBI
1-{[2-(diethylamino)ethyl]amino}-4-methylthioxanthen-9-one
ChEBI
lucanthone
ChemIDplus
lucanthone
WHO_MedNet
lucanthonum
ChemIDplus
lucantona
ChemIDplus
A drug that modulates the function of the endocrine glands, the biosynthesis of their secreted hormones, or the action of hormones upon their specific sites.
hormone receptor modulators
hormone receptor modulator
hormone receptor modulators
ChEBI
organic halide salts
organic halide salt
organic halide salts
ChEBI
3-(diethylamino)-7-{(E)-[4-(dimethylamino)phenyl]diazenyl}-5-phenylphenazin-5-ium
Janus Green B cation
3-(diethylamino)-7-{(E)-[4-(dimethylamino)phenyl]diazenyl}-5-phenylphenazin-5-ium
IUPAC
nitrate salts
nitrate salt
nitrate salts
ChEBI
inorganic nitrate salts
inorganic nitrates
inorganic nitrate salt
inorganic nitrate salts
ChEBI
inorganic nitrates
ChEBI
A role played by the molecular entity or part thereof within a chemical context.
chemical role
Nitrogenous compounds
nitrogen compounds
nitrogen molecular entities
nitrogen molecular entity
Nitrogenous compounds
KEGG_COMPOUND
nitrogen compounds
ChEBI
nitrogen molecular entities
ChEBI
nitrogen group
nitrogen groups
nitrogen-containing group
nitrogenous group
nitrogen group
nitrogen group
ChEBI
nitrogen groups
ChEBI
nitrogen-containing group
ChEBI
nitrogenous group
ChEBI
An organic molecule that is electrically neutral carrying a positive and a negative charge in one of its major canonical descriptions. In most dipolar compounds the charges are delocalized; however the term is also applied to species where this is not the case.
dipolar compounds
dipolar compound
dipolar compounds
ChEBI
diamminedichloridoplatinum
diamminedichloridoplatinum(II)
diamminedichloroplatinum
diamminedichloroplatinum(II)
diammine(dichloro)platinum
diammineplatinum dichloride
diamminedichloroplatinum
diamminedichloridoplatinum
IUPAC
diamminedichloridoplatinum(II)
IUPAC
diamminedichloroplatinum
IUPAC
diamminedichloroplatinum(II)
IUPAC
diammine(dichloro)platinum
ChEBI
diammineplatinum dichloride
NIST_Chemistry_WebBook
Sulfate salts where the cation is a metal ion.
metal sulfates
metal sulfate
metal sulfates
ChEBI
A substance, such as agonists, antagonists, degradation or uptake inhibitors, depleters, precursors, and modulators of receptor function, used for its pharmacological actions on GABAergic systems.
GABA agent
Any organic substituent group, regardless of functional type, having two free valences at carbon atom(s).
organodiyl groups
organodiyl group
organodiyl groups
ChEBI
organic divalent group
organic univalent group
A carboxamide resulting from the formal condensation of a carboxylic acid with the amino group of an amino acid.
N-acyl amino acid
N-acyl amino acids
N-acyl-amino-acid
N-acyl-amino-acids
N-acylamino acid
N-acylamino acids
acyl-amino-acid
acyl-amino-acids
acylamino acids
N-acyl-amino acid
N-acyl amino acid
ChEBI
N-acyl amino acids
ChEBI
N-acyl-amino-acid
ChEBI
N-acyl-amino-acids
ChEBI
N-acylamino acid
ChEBI
N-acylamino acids
ChEBI
acyl-amino-acid
ChEBI
acyl-amino-acids
ChEBI
acylamino acids
ChEBI
An alpha,beta-unsaturated ketone of general formula R(1)R(2)C=CR(3)-C(=O)R(4) (R(4) =/= H) in which the C=O function is conjugated to a C=C double bond at the alpha,beta position.
enones
enone
enones
ChEBI
A ketone of general formula R(1)R(2)C=CR(3)-C(=O)R(4) (R(4) =/= H) or R(1)C#C-C(=O)R(2) (R(2) =/= H) in which the ketonic C=O function is conjugated to an unsaturated C-C bond at the alpha,beta position.
alpha,beta-unsaturated ketones
alpha,beta-unsaturated ketone
alpha,beta-unsaturated ketones
ChEBI
Acridines which are substituted in any position by one or more amino groups or substituted amino groups. Note that the term 'aminoacridine' is the International Prorietary Name (INN) for 9-aminoacridine.
aminoacridine
aminoacridines
aminoacridine
ChEBI
organic polycyclic compounds
organic polycyclic compound
organic polycyclic compounds
ChEBI
organic tricyclic compounds
organic tricyclic compound
organic tricyclic compounds
ChEBI
An organic anion that is the conjugate base of methanol.
methoxide ion
methoxide
methoxide ion
ChEBI
A racemate comprising equimolar amounts of (2S)-gluphosinate (better known as gluphosinate-P) and (2R)-gluphosinate.
glufosinate
rac-2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid
(+-)-phosphinothricin
(2RS)-2-amino-4-[hydroxy(methyl)phosphinoyl]butyric acid
2-Amino-4-(hydroxymethylphosphinyl)butanoic acid
3-Amino-3-carboxypropylmethylphosphinic acid
4-[hydroxy(methyl)phosphinoyl]-DL-homoalanine
DL-2-Amino-4-(methylphosphino)butanoic acid
DL-phosphinothricin
phosphinothricin
rac-glufosinate
glufosinate
glufosinate
ChemIDplus
rac-2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid
IUPAC
(+-)-phosphinothricin
ChemIDplus
(2RS)-2-amino-4-[hydroxy(methyl)phosphinoyl]butyric acid
Alan_Wood's_Pesticides
2-Amino-4-(hydroxymethylphosphinyl)butanoic acid
KEGG_COMPOUND
3-Amino-3-carboxypropylmethylphosphinic acid
ChemIDplus
4-[hydroxy(methyl)phosphinoyl]-DL-homoalanine
Alan_Wood's_Pesticides
DL-2-Amino-4-(methylphosphino)butanoic acid
ChemIDplus
DL-phosphinothricin
ChemIDplus
phosphinothricin
KEGG_COMPOUND
rac-glufosinate
ChEBI
A biological role played by the molecular entity or part thereof within a biochemical context.
biochemical role
biophysical role
A role played by the molecular entity or part thereof which causes the development of a pathological process.
etiopathogenetic agent
etiopathogenetic role
aetiopathogenetic role
etiopathogenetic agent
ChEBI
etiopathogenetic role
ChEBI
A biological role which describes how a drug interacts within a biological system and how the interactions affect its medicinal properties.
pharmacological role
physiological role
Any substance introduced into a living organism with therapeutic or diagnostic purpose.
farmaco
medicament
pharmaceuticals
pharmaceutical
farmaco
ChEBI
medicament
ChEBI
pharmaceuticals
ChEBI
A compound with the general formula R2C=O (R=/=H) where one or more of the R groups contains an oxy (-O-) group.
oxyketones
oxyketone
oxyketones
ChEBI
An oxyketone with the general formula R2C(=O) (R=/=H) where one or more of the R groups contains an oxy (-O-) group and the oxy and carbonyl groups are bonded to the same carbon atom.
alpha-oxyketones
alpha-oxyketone
alpha-oxyketones
ChEBI
jasmonate ester
jasmonate ester
jasmonate ester
ChEBI
A tryptophan derivative that is tryptophan substituted by a methyl group at position 5 of the indole ring.
5-methyltryptophan
inorganic hydroxides
inorganic hydroxy compound
inorganic hydroxides
ChEBI
A member of the class of butanediols that is butane in which two of the hydrogens have been replaced by hydroxy groups.
butanediol
butanediols
butanediol
butanediol
IUPAC
butanediols
ChEBI
(9Z,12Z,15Z)-octadeca-9,12,15-trienoate
The biological role played by a material entity when bound by a receptor of the adaptive immune system. Specific site on an antigen to which an antibody binds.
antigenic determinant
epitope function
epitope role
epitope
antigenic determinant
ChEBI
epitope function
ChEBI
epitope role
ChEBI
An antagonist at the A2A receptor.
adenosine A2A receptor antagonists
adenosine A2A receptor antagonist
adenosine A2A receptor antagonists
ChEBI
A compound arising from loss of part of the carotene skeleton (excluding retinoids)
apo carotenoids
apocarotenoid
apocarotenoids
apo carotenoid
apo carotenoids
ChEBI
apocarotenoid
ChEBI
apocarotenoids
ChEBI
Any fatty acid containing at least one C=C double bond.
olefinic fatty acid
2-amino-2-deoxyglucose
Glucosamine
glucosamine
2-Amino-2-deoxy-glucose
GlcN
Glucosamin
Glukosamin
glucosamine
2-amino-2-deoxyglucose
IUPAC
Glucosamine
KEGG_COMPOUND
glucosamine
IUPAC
2-Amino-2-deoxy-glucose
KEGG_COMPOUND
GlcN
JCBN
Glucosamin
ChEBI
Glukosamin
ChEBI
Any one of a large family of chemically related mycotoxins with a structure based on a sesquiterpene skeleton. The most important structural features causing the biological activities of trichothecenes are a 12,13-epoxy ring, the presence of hydroxy or acetyl groups at appropriate positions on the trichothecene nucleus and the structure and position of the side-chain.
trichothecenes
trichothecene
trichothecenes
ChEBI
A cyclic compound having as ring members atoms of at least two different elements.
Heterocyclic compound
compuesto heterociclico
compuestos heterociclicos
heterocycle
heterocyclic compounds
heterocyclic compound
Heterocyclic compound
KEGG_COMPOUND
compuesto heterociclico
IUPAC
compuestos heterociclicos
IUPAC
heterocycle
ChEBI
heterocyclic compounds
ChEBI
An amino acid zwitterion arising from transfer of a proton from the carboxy to the amino group of glycine.
2-azaniumylacetate
glycine
glycine zwitterion
2-azaniumylacetate
IUPAC
glycine
UniProt
A flavonoid oxoanion that is the conjugate base of luteolin, arising from selective deprotonation of the 7-hydroxy group.
2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-olate
2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-1-benzopyran-7-olate
luteolin
luteolin-7-olate anion
luteolin-7-olate
2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-olate
IUPAC
2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-1-benzopyran-7-olate
IUPAC
luteolin
UniProt
luteolin-7-olate anion
ChEBI
A fatty acid anion with a chain length of C13 to C22.
a long-chain carboxylate
a long-chain fatty acid
long-chain fatty acid anions
long-chain fatty acid anion
a long-chain carboxylate
ChEBI
a long-chain fatty acid
UniProt
long-chain fatty acid anions
ChEBI
A cyclic tetrapyrrole anion that is the conjugate base of chlorophyllide a arising from deprotonation of the carboxy group; major species at pH 7.3.
chlorophyllide a anion
chlorophyllide a(1-)
chlorophyllide a anion
ChEBI
A D-alpha-amino acid zwitterion that is D-phenylalanine in which a proton has been transferred from the carboxy group to the amino group. It is the major species at pH 7.3.
(2R)-2-azaniumyl-3-phenylpropanoate
(2R)-2-ammonio-3-phenylpropanoate
D-phenylalanine
D-phenylalanine zwitterion
(2R)-2-azaniumyl-3-phenylpropanoate
IUPAC
(2R)-2-ammonio-3-phenylpropanoate
IUPAC
D-phenylalanine
UniProt
An amino acid zwitterion arising from transfer of a proton from the carboxy to the amino group of L-phenylalanine; major species at pH 7.3.
(2S)-2-azaniumyl-3-phenylpropanoate
(2S)-2-ammonio-3-phenylpropanoate
L-phenylalanine
phenylalanine
L-phenylalanine zwitterion
(2S)-2-azaniumyl-3-phenylpropanoate
IUPAC
(2S)-2-ammonio-3-phenylpropanoate
IUPAC
L-phenylalanine
UniProt
phenylalanine
ChEBI
A cyclic tetrapyrrole anion arising from deprotonation at the 21-position of chlorophyll a.
chlorophyll a
chlorophyll a(1-)
chlorophyll a
UniProt
A 5-oxo monocarboxylic acid anion resulting from the removal of a proton from the carboxy group of jasmonic acid. The major species at pH 7.3.
{(1R,2R)-3-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl}acetate
jasmonate
jasmonate(1-)
{(1R,2R)-3-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl}acetate
IUPAC
jasmonate
UniProt
The conjugate base of an N-acetyl-D-amino acid.
N-acetyl-D-amino acetate(1-)
N-acetyl-D-amino acid anions
N-acetyl-D-amino carboxylate anions
an N-acetyl-D-amino acid
N-acetyl-D-amino acid anion
N-acetyl-D-amino acetate(1-)
ChEBI
N-acetyl-D-amino acid anions
ChEBI
N-acetyl-D-amino carboxylate anions
ChEBI
an N-acetyl-D-amino acid
UniProt
Conjugate base of an N-acyl-L-aspartic acid.
N-acyl-L-aspartate
N-acyl-L-aspartate(2-)
N-acyl-L-aspartate
UniProt
A gibberellin carboxylic acid anion obtained by deprotonation of the carboxy group of gibberellin A3.
(1R,2R,5S,8S,9S,10R,11S,12S)-5,12-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1(5,8).0(1,10).0(2,8)]heptadec-13-ene-9-carboxylate
2beta,7alpha-dihydroxy-1beta-methyl-8-methylidene-13-oxo-4a,1alpha-epoxymethano-4aalpha,4bbeta-gibb-3-ene-10beta-carboxylate
gibberellin A3
gibberellin A3(1-)
(1R,2R,5S,8S,9S,10R,11S,12S)-5,12-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1(5,8).0(1,10).0(2,8)]heptadec-13-ene-9-carboxylate
IUPAC
2beta,7alpha-dihydroxy-1beta-methyl-8-methylidene-13-oxo-4a,1alpha-epoxymethano-4aalpha,4bbeta-gibb-3-ene-10beta-carboxylate
IUPAC
gibberellin A3
UniProt
A cyclic tetrapyrrole anion that is the conjugate base of chlorophyllide b, arising from deprotonation of the carboxy group.
chlorophyllide b anion
chlorophyllide b(1-)
chlorophyllide b anion
ChEBI
Conjugate base of phosphinothricin arising from deprotonation of the phosphinate function.
2-azaniumyl-4-(methylphosphinato)butanoate
2-ammonio-4-(methylphosphinato)butanoate
phosphinothricin
phosphinothricin(1-)
2-azaniumyl-4-(methylphosphinato)butanoate
IUPAC
2-ammonio-4-(methylphosphinato)butanoate
ChEBI
phosphinothricin
UniProt
An organic anion arising from deprotonation of a cyclic tetrapyrrole compound.
cyclic tetrapyrrole anions
cyclic tetrapyrrole anion
cyclic tetrapyrrole anions
ChEBI
An organic phosphoric acid derivative in which one or more oxygen atoms of the phosphate group(s) has been deprotonated.
organophosphate oxoanions
organophosphate oxoanion
organophosphate oxoanions
ChEBI
Any fatty acid anion obtained by removal of a proton from the carboxy group of a short-chain fatty acid (chain length of less than C6).
a short-chain fatty acid
short-chain fatty acid anions
short-chain fatty acid anion
a short-chain fatty acid
UniProt
short-chain fatty acid anions
ChEBI
Any fatty acid anion in which there is no C-C unsaturation.
saturated fatty acid anions
saturated fatty acid anion
saturated fatty acid anions
ChEBI
Any saturated fatty acid anion lacking a carbon side-chain.
straight-chain saturated fatty acid anions
straight-chain saturated fatty acid anion
straight-chain saturated fatty acid anions
ChEBI
An organic anion of general formula RS(=O)2O(-) where R is an organyl group.
organosulfate oxoanions
organosulfate oxoanion
organosulfate oxoanions
ChEBI
A carboxylic acid anion arising from deprotonation of one or more carboxy groups of any gibberellin.
gibberellin monocarboxylic acid anions
gibberellin carboxylic acid anion
gibberellin monocarboxylic acid anions
ChEBI
A substance used as an indicator of a biological state.
biological marker
biomarker
biological marker
ChEBI
Any substance capable of eliciting an immune response only when attached to a large carrier such as a protein. Examples include dinitrophenols; oligosaccharides; peptides; and heavy metals.
haptens
hapten
haptens
ChEBI
Any fatty acid whose skeletal carbon atoms form an unbranched open chain.
straight-chain fatty acids
straight-chain fatty acid
straight-chain fatty acids
ChEBI
A fatty acid anion formed by deprotonation of the carboxylic acid functional group of a straight-chain fatty acid.
straight-chain FA anion
straight-chain FA anions
straight-chain fatty acid anions
straight-chain fatty acid anion
straight-chain FA anion
ChEBI
straight-chain FA anions
ChEBI
straight-chain fatty acid anions
ChEBI
Any member of the sub-set of polyunsaturated fatty acid for which there is an absolute dietary requirement.
EFA
EFAs
EFS
acides gras indispensables
acidos grasos esenciales
essential fatty acids
essentielle Fettsaeuren
essential fatty acid
EFA
ChEBI
EFAs
ChEBI
EFS
ChEBI
acides gras indispensables
ChEBI
acidos grasos esenciales
ChEBI
essential fatty acids
ChEBI
essentielle Fettsaeuren
ChEBI
Compounds containing one or more phosphoric acid units.
phosphoric acids
A reagent that forms a bond to its reaction partner (the nucleophile) by accepting both bonding electrons from that reaction partner.
electrophile
electrophiles
electrophilic reagents
electrophilic reagent
electrophile
ChEBI
electrophiles
ChEBI
electrophilic reagents
ChEBI
A reagent that forms a bond to its reaction partner (the electrophile) by donating both bonding electrons.
nucleophile
nucleophiles
nucleophilic reagents
nucleophilic reagent
nucleophile
ChEBI
nucleophiles
ChEBI
nucleophilic reagents
ChEBI
Hydroxy boron compounds of general formula BxOyHz.
boric acids
Conjugate base of an L-alpha-amino acid arising from deprotonation of the C-1 carboxy group.
L-alpha-amino carboxylate
L-alpha-amino acid anion
L-alpha-amino carboxylate
ChEBI
Zwitterionic form of an L-alpha-amino acid having an anionic carboxy group and a protonated amino group.
L-alpha-amino acid zwitterions
an L-alpha-amino acid
L-alpha-amino acid zwitterion
L-alpha-amino acid zwitterions
ChEBI
an L-alpha-amino acid
UniProt
Zwitterionic form of a D-alpha-amino acid having an anionic carboxy group and a protonated amino group.
D-alpha-amino acid zwitterions
a D-alpha-amino acid
D-alpha-amino acid zwitterion
D-alpha-amino acid zwitterions
ChEBI
a D-alpha-amino acid
UniProt
A carboxylic acid anion that is the conjugate base of an N-acyl-L-alpha-amino acid arising from deprotonation of the C-1 carboxy group.
N-acyl-L-alpha-amino acid(1-)
an N-acyl-L-amino acid
N-acyl-L-alpha-amino acid anion
N-acyl-L-alpha-amino acid(1-)
ChEBI
an N-acyl-L-amino acid
UniProt
The conjugate base of an N-acyl-D-alpha-amino acid arising from deprotonation of the C-1 carboxy group.
N-acyl-D-alpha-amino acid(1-)
an N-acyl-D-amino acid
N-acyl-D-alpha-amino acid anion
N-acyl-D-alpha-amino acid(1-)
ChEBI
an N-acyl-D-amino acid
UniProt
A chemical substance is a portion of matter of constant composition, composed of molecular entities of the same type or of different types.
Chemische Substanz
chemical substance
Chemische Substanz
ChEBI
A mixture is a chemical substance composed of multiple molecules, at least two of which are of a different kind.
Mischung
mixture
Mischung
ChEBI
Any anion arising from deprotonation of at least one OH group in a flavonoid compound.
flavonoid oxoanions
flavonoid oxoanion
flavonoid oxoanions
ChEBI
A metal cation with a valence of two.
a divalent metal cation
divalent metal cation
a divalent metal cation
UniProt
An atom or small molecule with a positive charge that does not contain carbon in covalent linkage, with a valency of one.
a monovalent cation
monovalent inorganic cation
a monovalent cation
UniProt
A nickel atom having a net electric charge.
nickel ion
R = C or H. The iminium ion resulting from the protonation of one of the imine nitrogens of guanidine or its derivatives.
diaminomethaniminium ion
diaminomethaniminium ions
guanidinium ions
guanidinium ion
diaminomethaniminium ion
ChEBI
diaminomethaniminium ions
ChEBI
guanidinium ions
ChEBI
Zwitterionic form of any peptide where, in general, the amino terminus is positively charged and the carboxy terminus is negatively charged.
a peptide
peptide zwitterions
peptide zwitterion
a peptide
UniProt
peptide zwitterions
ChEBI
Any member of the class of herbicides whose members contain a phenoxy or substituted phenoxy group.
phenoxy herbicides
phenoxy herbicide
phenoxy herbicides
ChEBI
Any pharmacological or immunological agent that modifies the effect of other agents such as drugs or vaccines while having few if any direct effects when given by itself.
adjuvants
adjuvant
adjuvants
ChEBI
Any substance that interacts with tubulin to inhibit or promote polymerisation of microtubules.
tubulin modulators
tubulin modulator
tubulin modulators
ChEBI
Any alpha-amino acid anion in which the parent amino acid has D-configuration.
D-alpha-amino acid anions
D-alpha-amino carboxylate
D-alpha-amino acid anion
D-alpha-amino acid anions
ChEBI
D-alpha-amino carboxylate
ChEBI
A racemate is an equimolar mixture of a pair of enantiomers.
melange racemique
racemates
racemic mixture
racemate
melange racemique
ChEBI
racemates
ChEBI
racemic mixture
ChEBI
Any amino sugar that is a monosaccharide in which one alcoholic hydroxy group is replaced by an amino group.
amino monosaccharides
amino monosaccharide
amino monosaccharides
ChEBI
A class of diterpene formed in plants in response to fungal infection, physical damage, chemical injury, or a pathogenic process; they are sometimes referred to as plant antibiotics. Diterpenes are unsaturated hydrocarbons containing 20 carbon atoms and 4 branched methyl groups and are made up of isoprenoid units.
diterpene phytoalexins
diterpenoid phytoalexin
diterpenoid phytoalexins
diterpene phytoalexin
diterpene phytoalexins
ChEBI
diterpenoid phytoalexin
ChEBI
diterpenoid phytoalexins
ChEBI
A poison that interferes with the function of the kidneys.
nephrotoxins
nephrotoxin
nephrotoxins
ChEBI
Any lipid carrying one or more hydroperoxy substituents.
a lipid hydroperoxide
lipid hydroperoxides
lipid hydroperoxide
a lipid hydroperoxide
UniProt
lipid hydroperoxides
ChEBI
Any compound that has a nucleobase as a part.
nucleobase-containing compound
nucleobase-containing compounds
nucleobase-containing molecular entities
nucleobase-containing molecular entity
nucleobase-containing compound
SUBMITTER
nucleobase-containing compounds
ChEBI
nucleobase-containing molecular entities
ChEBI
A dicarboxylate that contains four carbon atoms.
C4-dicarboxylate
carbamimidoylazanium
The cyclic tetrapyrrole anion that is chlorophyll b protonated to pH 7.3.
[methyl (3S,4S)-9-ethenyl-14-ethyl-13-formyl-4,8,18-trimethyl-20-oxo-3-(3-oxo-3-{[(2E,7R,11R)-3,7,11,15-tetramethylhexadec-2-en-1-yl]oxy}propyl)phorbine-21-carboxylatato(3-)-kappaN(23),kappa(4)N(24),kappaN(25),kappaN(26)]magnesate(1-)
chlorophyll b
chlorophyll b(1-)
[methyl (3S,4S)-9-ethenyl-14-ethyl-13-formyl-4,8,18-trimethyl-20-oxo-3-(3-oxo-3-{[(2E,7R,11R)-3,7,11,15-tetramethylhexadec-2-en-1-yl]oxy}propyl)phorbine-21-carboxylatato(3-)-kappaN(23),kappa(4)N(24),kappaN(25),kappaN(26)]magnesate(1-)
IUPAC
chlorophyll b
UniProt
Any substance that interacts with tubulin to inhibit polymerisation of microtubules.
microtubule destabilising agent
microtubule destabilising agents
microtubule destabilising role
microtubule destabilizing role
microtubule-destabilising agents
microtubule-destabilizing agent
microtubule-destabilizing agents
microtubule-destabilising agent
microtubule destabilising agent
ChEBI
microtubule destabilising agents
ChEBI
microtubule destabilising role
ChEBI
microtubule destabilizing role
SUBMITTER
microtubule-destabilising agents
ChEBI
microtubule-destabilizing agent
ChEBI
microtubule-destabilizing agents
ChEBI
Zwitterionic form of a polar amino acid having an anionic carboxy group and a protonated amino group.
a polar amino acid
polar amino acid zwitterion
a polar amino acid
UniProt
A monocarboxylic acid anion that is the conjugate base of cis-abscisic acid; major species at pH 7.3.
2-cis-abscisate anion
2-cis-abscisate(1-)
2-cis-abscisic acid anion
abscisate
abscisate anion
abscisate(1-)
abscisic acid anion
2-cis-abscisate
2-cis-abscisate anion
ChEBI
2-cis-abscisate(1-)
ChEBI
2-cis-abscisic acid anion
ChEBI
abscisate
ChEBI
abscisate anion
ChEBI
abscisate(1-)
ChEBI
abscisic acid anion
ChEBI
An alkanesulfonate in which the carbon at position 1 is attached to at least two hydrogens.
1,1-di-unsubstituted alkanesulfonate
1,1-di-unsubstituted alkanesulfonates
1,1-diunsubstituted alkanesulfonates
1,1-diunsubstituted alkanesulfonate
1,1-di-unsubstituted alkanesulfonate
ChEBI
1,1-di-unsubstituted alkanesulfonates
ChEBI
1,1-diunsubstituted alkanesulfonates
ChEBI
Any apo carotenoid sesquiterpenoid that is 3-methylpenta-2,4-dienoic acid substituted at position 5 by a 1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl group and in which the acyclic double bond between positions 4 and 5 has E-configuration.
(4E)-5-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-3-methylpenta-2,4-dienoic acid
abscisic acid
abscisic acids
(4E)-5-(1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl)-3-methylpenta-2,4-dienoic acid
IUPAC
abscisic acid
ChEBI
A monocarboxylic acid anion obtained by removal of a proton from the carboxy group of any member of the class of abscisic acids.
abscisate
abscisates
abscisate
UniProt
The dicarboxylic acid dianion formed from folic acid by loss of a proton from each of the two carboxy groups in the glutamic acid moiety.
N-(4-{[(2-amino-4-oxo-3,4-dihydropteridin-6-yl)methyl]amino}benzoyl)-L-glutamate(2-)
folate
pteroyl-L-glutamate
pteroyl-L-monoglutamate
pteroylglutamate
folate(2-)
N-(4-{[(2-amino-4-oxo-3,4-dihydropteridin-6-yl)methyl]amino}benzoyl)-L-glutamate(2-)
IUPAC
folate
MetaCyc
folate
UniProt
pteroyl-L-glutamate
ChEBI
pteroyl-L-monoglutamate
ChEBI
pteroylglutamate
ChEBI
A family of nitrogen molecular entities which are highly reactive and derived from nitric oxide (.NO) and superoxide (O2.(-)) produced via the enzymatic activity of inducible nitric oxide synthase 2 (NOS2) and NADPH oxidase respectively.
RNI
RNS
reactive nitrogen species
RNI
SUBMITTER
RNS
SUBMITTER
Any additive that enhances the efficiency of fuel.
fuel additives
fuel enhancer
fuel additive
fuel additives
ChEBI
fuel enhancer
ChEBI
Any compound that is able to prevent damage to the liver.
antihepatotoxic agent
hepatoprotective agents
hepatoprotector
hepatoprotective agent
antihepatotoxic agent
ChEBI
hepatoprotective agents
ChEBI
hepatoprotector
ChEBI
An inorganic sulfate salt obtained by reaction of sulfuric acid with two equivalents of ammonia. A high-melting (decomposes above 280degreeC) white solid which is very soluble in water (70.6 g/100 g water at 0degreeC; 103.8 g/100 g water at 100degreeC), it is widely used as a fertilizer for alkaline soils.
diazanium sulfate
(NH4)2SO4
ammonium sulfate (2:1)
ammonium sulphate
diammonium sulfate
mascagnite
sulfuric acid ammonium salt (1:2)
sulfuric acid, diammonium salt
sulphate of ammonia
ammonium sulfate
diazanium sulfate
IUPAC
(NH4)2SO4
ChEBI
ammonium sulfate (2:1)
ChemIDplus
ammonium sulphate
SUBMITTER
diammonium sulfate
IUPAC
mascagnite
ChemIDplus
sulfuric acid ammonium salt (1:2)
ChemIDplus
sulfuric acid, diammonium salt
ChemIDplus
sulphate of ammonia
ChEBI
The inorganic nitrate salt of sodium.
sodium nitrate
sodium trioxidonitrate(1-)
Chile saltpeter
Cubic niter
Niter
Nitrate de sodium
Nitrate of soda
Nitric acid monosodium salt
Nitric acid sodium salt (1:1)
Nitric acid, sodium salt
Sodium saltpeter
Sodium(I) nitrate (1:1)
sodium nitrate
sodium nitrate
IUPAC
sodium trioxidonitrate(1-)
IUPAC
Chile saltpeter
SUBMITTER
Cubic niter
ChemIDplus
Niter
ChemIDplus
Nitrate de sodium
ChemIDplus
Nitrate of soda
ChemIDplus
Nitrate of soda
SUBMITTER
Nitric acid monosodium salt
ChemIDplus
Nitric acid sodium salt (1:1)
ChemIDplus
Nitric acid, sodium salt
ChemIDplus
Sodium saltpeter
ChemIDplus
Sodium(I) nitrate (1:1)
ChemIDplus
The ammonium salt of nitric acid.
ammonium nitrate
Ammonium nitricum
Ammonium saltpeter
Ammonium(I) nitrate (1:1)
Nitrate d'ammonium
Nitrate of ammonia
Nitrato amonico
Nitric acid ammonium salt (1:1)
Nitric acid, ammonium salt
Norway saltpeter
ammonium nitrate
ammonium nitrate
IUPAC
Ammonium nitricum
ChemIDplus
Ammonium saltpeter
ChemIDplus
Ammonium(I) nitrate (1:1)
ChemIDplus
Nitrate d'ammonium
ChemIDplus
Nitrate of ammonia
ChemIDplus
Nitrato amonico
ChemIDplus
Nitric acid ammonium salt (1:1)
ChemIDplus
Nitric acid, ammonium salt
ChemIDplus
Norway saltpeter
ChemIDplus
The inorganic nitrate salt of potassium.
potassium nitrate
Kaliumnitrat
Niter
Nitrate of potash
Nitre
Nitric acid, potassium salt
Salt peter
Saltpeter
saltpetre
potassium nitrate
potassium nitrate
IUPAC
Kaliumnitrat
ChemIDplus
Niter
ChemIDplus
Nitrate of potash
ChemIDplus
Nitre
ChemIDplus
Nitric acid, potassium salt
ChemIDplus
Salt peter
ChemIDplus
Saltpeter
ChemIDplus
saltpetre
SUBMITTER
The chemical role played by a substance that stabilizes an emulsion by increasing its kinetic stability.
emulgent
emulgents
emulsifiers
emulsifier
emulgent
ChEBI
emulgents
ChEBI
emulsifiers
ChEBI
Any zinc ion that is positively charged.
zinc cations
zinc cation
zinc cations
ChEBI
A transition element cation where the metal is specifed as cadmium.
cadmium cations
cadmium cation
cadmium cations
ChEBI
A carbohydrate derivative arising formally from the elimination of water from a glycosidic hydroxy group and an H atom bound to an oxygen, carbon, nitrogen or sulfur atom of a separate entity.
glycosyl compounds
glycosyl compound
glycosyl compounds
ChEBI
The element or compound in a reduction-oxidation (redox) reaction that donates an electron to another species.
reducer
reducers
reducing agents
reductant
reductants
reducing agent
reducer
ChEBI
reducers
ChEBI
reducing agents
ChEBI
reductant
ChEBI
reductants
ChEBI
A substance that removes electrons from another reactant in a redox reaction.
oxidant
oxidants
oxidiser
oxidisers
oxidising agents
oxidizer
oxidizers
oxidizing agent
oxidizing agents
oxidising agent
oxidant
ChEBI
oxidants
ChEBI
oxidiser
ChEBI
oxidisers
ChEBI
oxidising agents
ChEBI
oxidizer
ChEBI
oxidizers
ChEBI
oxidizing agent
ChEBI
oxidizing agents
ChEBI
Any organooxygen compound derived from a carbohydrate by replacement of one or more hydroxy group(s) by an amino group, a thiol group or similar heteroatomic groups. The term also includes derivatives of these compounds.
carbohydrate derivatives
derivatised carbohydrate
derivatised carbohydrates
derivatized carbohydrate
derivatized carbohydrates
carbohydrate derivative
carbohydrate derivatives
ChEBI
derivatised carbohydrate
ChEBI
derivatised carbohydrates
ChEBI
derivatized carbohydrate
ChEBI
derivatized carbohydrates
ChEBI
An EC 3.1.3.* (phosphoric monoester hydrolase) inhibitor that interferes with the action of alkaline phosphatase (EC 3.1.3.1).
EC 3.1.3.1 (alkaline phosphatase) inhibitors
EC 3.1.3.1 inhibitor
EC 3.1.3.1 inhibitors
alkaline phenyl phosphatase inhibitor
alkaline phenyl phosphatase inhibitors
alkaline phosphatase (EC 3.1.3.1) inhibitor
alkaline phosphatase (EC 3.1.3.1) inhibitors
alkaline phosphatase inhibitor
alkaline phosphatase inhibitors
alkaline phosphohydrolase inhibitor
alkaline phosphohydrolase inhibitors
alkaline phosphomonoesterase inhibitor
alkaline phosphomonoesterase inhibitors
glycerophosphatase inhibitor
glycerophosphatase inhibitors
orthophosphoric-monoester phosphohydrolase (alkaline optimum) inhibitor
orthophosphoric-monoester phosphohydrolase (alkaline optimum) inhibitors
phosphate-monoester phosphohydrolase (alkaline optimum) inhibitor
phosphate-monoester phosphohydrolase (alkaline optimum) inhibitors
phosphomonoesterase inhibitor
phosphomonoesterase inhibitors
EC 3.1.3.1 (alkaline phosphatase) inhibitor
EC 3.1.3.1 (alkaline phosphatase) inhibitors
ChEBI
EC 3.1.3.1 inhibitor
ChEBI
EC 3.1.3.1 inhibitors
ChEBI
alkaline phenyl phosphatase inhibitor
ChEBI
alkaline phenyl phosphatase inhibitors
ChEBI
alkaline phosphatase (EC 3.1.3.1) inhibitor
ChEBI
alkaline phosphatase (EC 3.1.3.1) inhibitors
ChEBI
alkaline phosphatase inhibitor
ChEBI
alkaline phosphatase inhibitors
ChEBI
alkaline phosphohydrolase inhibitor
ChEBI
alkaline phosphohydrolase inhibitors
ChEBI
alkaline phosphomonoesterase inhibitor
ChEBI
alkaline phosphomonoesterase inhibitors
ChEBI
glycerophosphatase inhibitor
ChEBI
glycerophosphatase inhibitors
ChEBI
orthophosphoric-monoester phosphohydrolase (alkaline optimum) inhibitor
ChEBI
orthophosphoric-monoester phosphohydrolase (alkaline optimum) inhibitors
ChEBI
phosphate-monoester phosphohydrolase (alkaline optimum) inhibitor
ChEBI
phosphate-monoester phosphohydrolase (alkaline optimum) inhibitors
ChEBI
phosphomonoesterase inhibitor
ChEBI
phosphomonoesterase inhibitors
ChEBI
A carbohydrate derivative that is formally obtained from a disaccharide.
disaccharide derivatives
disaccharide derivative
disaccharide derivatives
ChEBI
A sulfur-containing amino acid whose alpha-carboxylic acid group is ionized (not protonated).
sulfur-containing amino-acid anions
sulfur-containing amino-acid anion
sulfur-containing amino-acid anions
ChEBI
An aromatic amino acid whose alpha-carboxylic acid group is ionized (non-protonated).
aromatic amino-acid anions
aromatic amino-acid anion
aromatic amino-acid anions
ChEBI
A substance capable of undergoing rapid and highly exothermic decomposition.
explosive compound
explosive compounds
explosive material
explosives
explosives chemical
explosives chemicals
explosive
explosive compound
ChEBI
explosive compounds
ChEBI
explosive material
ChEBI
explosives
ChEBI
explosives chemical
ChEBI
explosives chemicals
ChEBI
Any compound that can be used for the treatment of neurodegenerative disorders.
neuroprotectant
neuroprotectants
neuroprotective agents
neuroprotective agent
neuroprotectant
ChEBI
neuroprotectants
ChEBI
neuroprotective agents
ChEBI
Any fatty acid carrying one or more hydroperoxy substituents.
hydroperoxy fatty acids
hydroperoxy fatty acid
hydroperoxy fatty acids
ChEBI
A fatty acid anion that is the conjugate base of any hydroperoxy fatty acid, formed by deprotonation of the carboxylic acid moiety.
hydroperoxy fatty acid anions
hydroperoxy fatty acid anion
hydroperoxy fatty acid anions
ChEBI
Any substance which is added to food to preserve or enhance its flavour and/or appearance.
food additives
food additive
food additives
ChEBI
A food additive that is used to change or otherwise control the acidity or alkalinity of foods. They may be acids, bases, neutralising agents or buffering agents.
acidity regulator
acidity regulators
food acidity regulators
pH control agent
pH control agents
food acidity regulator
acidity regulator
ChEBI
acidity regulators
ChEBI
food acidity regulators
ChEBI
pH control agent
ChEBI
pH control agents
ChEBI
Inorganic nitrate salt of calcium.
calcium dinitrate
Calcium saltpeter
Calcium(II) nitrate (1:2)
Lime nitrate
Lime saltpeter
Nitric acid, calcium salt
Norge saltpeter
Norway saltpeter
Norwegian saltpeter
Saltpeter
anhydrous calcium nitrate
calcium nitrate
calcium dinitrate
IUPAC
Calcium saltpeter
ChemIDplus
Calcium(II) nitrate (1:2)
ChemIDplus
Lime nitrate
ChemIDplus
Lime saltpeter
ChemIDplus
Nitric acid, calcium salt
ChemIDplus
Norge saltpeter
ChemIDplus
Norway saltpeter
ChemIDplus
Norwegian saltpeter
ChemIDplus
Saltpeter
ChemIDplus
anhydrous calcium nitrate
ChEBI
A compound used to form the matrix for MALDI (matrix-assisted laser desorption/ionization) mass spectrometry. MALDI matrix materials are crystalline compounds with a fairly low molecular weight, so as to allow facile vaporization, have strong absorption at UV or IR wavelengths (to rapidly and efficiently absorb laser irradiation), generally contain polar groups (enabling them to be used in aqueous solutions) and are frequently acidic (so assisting ionisation of the compound being studied, which is contained within the matrix material).
'matrix-assisted laser desorption/ionization' matrix material
'matrix-assisted laser desorption/ionization' matrix materials
MALDI matrix materials
MALDI matrix solution
MALDI matrix solutions
MALDI matrix material
'matrix-assisted laser desorption/ionization' matrix material
ChEBI
'matrix-assisted laser desorption/ionization' matrix materials
ChEBI
MALDI matrix materials
ChEBI
MALDI matrix solution
ChEBI
MALDI matrix solutions
ChEBI
An amino acid zwitterion obtained by transfer of a proton from the carboxy to the amino group of tryptophan; major species at pH 7.3.
2-azaniumyl-3-(1H-indol-3-yl)propanoate
2-ammonio-3-(1H-indol-3-yl)propanoate
tryptophan zwitterion
2-azaniumyl-3-(1H-indol-3-yl)propanoate
IUPAC
2-ammonio-3-(1H-indol-3-yl)propanoate
IUPAC
A polyphenylpropanoid derived from three monolignol monomers: trans-p-coumaryl alcohol, coniferol and trans-sinapyl alcohol. There is extensive cross-linking and no defined primary structure.
lignin
An EC 2.1.2.* (hydroxymethyl-, formyl- and related transferases) inhibitor that interferes with the action of glycine hydroxymethyltransferase (EC 2.1.2.1).
5,10-methylenetetrahydrofolate:glycine hydroxymethyltransferase inhibitor
5,10-methylenetetrahydrofolate:glycine hydroxymethyltransferase inhibitors
EC 2.1.2.1 (glycine hydroxymethyltransferase) inhibitors
EC 2.1.2.1 inhibitor
EC 2.1.2.1 inhibitors
L-serine hydroxymethyltransferase inhibitor
L-serine hydroxymethyltransferase inhibitors
L-threonine aldolase inhibitor
L-threonine aldolase inhibitors
allothreonine aldolase inhibitor
allothreonine aldolase inhibitors
glycine hydroxymethyltransferase (EC 2.1.2.1) inhibitor
glycine hydroxymethyltransferase (EC 2.1.2.1) inhibitors
glycine hydroxymethyltransferase inhibitor
glycine hydroxymethyltransferase inhibitors
serine aldolase inhibitor
serine aldolase inhibitors
serine hydroxymethylase inhibitor
serine hydroxymethylase inhibitors
serine hydroxymethyltransferase inhibitor
serine hydroxymethyltransferase inhibitors
serine transhydroxymethylase inhibitor
serine transhydroxymethylase inhibitors
threonine aldolase inhibitor
threonine aldolase inhibitors
EC 2.1.2.1 (glycine hydroxymethyltransferase) inhibitor
5,10-methylenetetrahydrofolate:glycine hydroxymethyltransferase inhibitor
ChEBI
5,10-methylenetetrahydrofolate:glycine hydroxymethyltransferase inhibitors
ChEBI
EC 2.1.2.1 (glycine hydroxymethyltransferase) inhibitors
ChEBI
EC 2.1.2.1 inhibitor
ChEBI
EC 2.1.2.1 inhibitors
ChEBI
L-serine hydroxymethyltransferase inhibitor
ChEBI
L-serine hydroxymethyltransferase inhibitors
ChEBI
L-threonine aldolase inhibitor
ChEBI
L-threonine aldolase inhibitors
ChEBI
allothreonine aldolase inhibitor
ChEBI
allothreonine aldolase inhibitors
ChEBI
glycine hydroxymethyltransferase (EC 2.1.2.1) inhibitor
ChEBI
glycine hydroxymethyltransferase (EC 2.1.2.1) inhibitors
ChEBI
glycine hydroxymethyltransferase inhibitor
ChEBI
glycine hydroxymethyltransferase inhibitors
ChEBI
serine aldolase inhibitor
ChEBI
serine aldolase inhibitors
ChEBI
serine hydroxymethylase inhibitor
ChEBI
serine hydroxymethylase inhibitors
ChEBI
serine hydroxymethyltransferase inhibitor
ChEBI
serine hydroxymethyltransferase inhibitors
ChEBI
serine transhydroxymethylase inhibitor
ChEBI
serine transhydroxymethylase inhibitors
ChEBI
threonine aldolase inhibitor
ChEBI
threonine aldolase inhibitors
ChEBI
An excitatory amino acid agonist which binds to NMDA receptors and triggers a response.
N-methyl-D-aspartate receptor agonist
N-methyl-D-aspartate receptor agonists
NMDA receptor agonists
NMDAR agonist
NMDAR agonists
NMDA receptor agonist
N-methyl-D-aspartate receptor agonist
ChEBI
N-methyl-D-aspartate receptor agonists
ChEBI
NMDA receptor agonists
ChEBI
NMDAR agonist
ChEBI
NMDAR agonists
ChEBI
A food additive which is added to flour or dough to improve baking quality and/or colour.
flour treatment agent
dough improver
dough improvers
improving agent
improving agents
flour treatment agent
flour treatment agent
ChEBI
dough improver
ChEBI
dough improvers
ChEBI
improving agent
ChEBI
improving agents
ChEBI
An inorganic cation with a valency of two.
divalent inorganic cation
An organic molecular entity containing a single carbon atom (C1).
one-carbon compounds
one-carbon compound
one-carbon compounds
ChEBI
Any organic molecular entity that is acidic and contains carbon in covalent linkage.
organic acids
organic acid
organic acids
ChEBI
The role played by a substance in enhancing the appearance or odour of the human body; a name given to the substance itself or to a component of it.
cosmetic component
cosmetics
cosmetic
cosmetic component
ChEBI
cosmetics
ChEBI
Any substance that causes disturbance to organisms by chemical reaction or other activity on the molecular scale, when a sufficient quantity is absorbed by the organism.
poisonous agent
poisonous agents
poisonous substance
poisonous substances
poisons
toxic agent
toxic agents
toxic substance
toxic substances
poison
poisonous agent
ChEBI
poisonous agents
ChEBI
poisonous substance
ChEBI
poisonous substances
ChEBI
poisons
ChEBI
toxic agent
ChEBI
toxic agents
ChEBI
toxic substance
ChEBI
toxic substances
ChEBI
Any compound that inhibits cell division (mitosis).
antimitotics
mitosis inhibitor
mitosis inhibitors
mitotic inhibitor
mitotic inhibitors
antimitotic
antimitotics
ChEBI
mitosis inhibitor
ChEBI
mitosis inhibitors
ChEBI
mitotic inhibitor
ChEBI
mitotic inhibitors
ChEBI
An antiparasitic drug which is effective against Apicomplexan parasites in the genus Plasmodium. The genus contains over 200 species and includes those responsible for malaria.
antiplasmodial agent
antiplasmodial agents
antiplasmodial drugs
antiplasmodium agent
antiplasmodium agents
antiplasmodium drug
antiplasmodium drugs
antiplasmodial drug
antiplasmodial agent
ChEBI
antiplasmodial agents
ChEBI
antiplasmodial drugs
ChEBI
antiplasmodium agent
ChEBI
antiplasmodium agents
ChEBI
antiplasmodium drug
ChEBI
antiplasmodium drugs
ChEBI
A lipoxygenase inhibitor that interferes with the action of arachidonate 15-lipoxygenase (EC 1.13.11.33).
15-LOX inhibitor
15-LOX inhibitors
15-lipoxygenase inhibitor
15-lipoxygenase inhibitors
EC 1.13.11.33 (arachidonate 15-lipoxygenase) inhibitors
EC 1.13.11.33 inhibitor
EC 1.13.11.33 inhibitors
arachidonate 15-lipoxygenase (EC 1.13.11.33) inhibitor
arachidonate 15-lipoxygenase (EC 1.13.11.33) inhibitors
arachidonate 15-lipoxygenase inhibitor
arachidonate 15-lipoxygenase inhibitors
arachidonate:oxygen 15-oxidoreductase inhibitor
arachidonate:oxygen 15-oxidoreductase inhibitors
linoleic acid omega(6)-lipoxygenase inhibitor
linoleic acid omega(6)-lipoxygenase inhibitors
omega(6) lipoxygenase inhibitor
omega(6) lipoxygenase inhibitors
EC 1.13.11.33 (arachidonate 15-lipoxygenase) inhibitor
15-LOX inhibitor
ChEBI
15-LOX inhibitors
ChEBI
15-lipoxygenase inhibitor
ChEBI
15-lipoxygenase inhibitors
ChEBI
EC 1.13.11.33 (arachidonate 15-lipoxygenase) inhibitors
ChEBI
EC 1.13.11.33 inhibitor
ChEBI
EC 1.13.11.33 inhibitors
ChEBI
arachidonate 15-lipoxygenase (EC 1.13.11.33) inhibitor
ChEBI
arachidonate 15-lipoxygenase (EC 1.13.11.33) inhibitors
ChEBI
arachidonate 15-lipoxygenase inhibitor
ChEBI
arachidonate 15-lipoxygenase inhibitors
ChEBI
arachidonate:oxygen 15-oxidoreductase inhibitor
ChEBI
arachidonate:oxygen 15-oxidoreductase inhibitors
ChEBI
linoleic acid omega(6)-lipoxygenase inhibitor
ChEBI
linoleic acid omega(6)-lipoxygenase inhibitors
ChEBI
omega(6) lipoxygenase inhibitor
ChEBI
omega(6) lipoxygenase inhibitors
ChEBI
Any EC 3.1.1.* (carboxylic ester hydrolase) inhibitor that inhibits the action of triacylglycerol lipase (EC 3.1.1.3).
EC 3.1.1.3 (triacylglycerol lipase) inhibitors
EC 3.1.1.3 inhibitor
EC 3.1.1.3 inhibitors
GEH inhibitor
GEH inhibitors
PPL inhibitor
PPL inhibitors
Tween hydrolase inhibitor
Tween hydrolase inhibitors
Tweenase inhibitor
Tweenase inhibitors
Tweenesterase inhibitor
Tweenesterase inhibitors
butyrinase inhibitor
butyrinase inhibitors
cacordase inhibitor
cacordase inhibitors
capalase L inhibitor
capalase L inhibitors
glycerol ester hydrolase inhibitor
glycerol ester hydrolase inhibitors
glycerol-ester hydrolase inhibitor
glycerol-ester hydrolase inhibitors
heparin releasable hepatic lipase inhibitor
heparin releasable hepatic lipase inhibitors
hepatic lipase inhibitor
hepatic lipase inhibitors
hepatic monoacylglycerol acyltransferase inhibitor
hepatic monoacylglycerol acyltransferase inhibitors
lipase inhibitor
lipase inhibitors
lipazin inhibitor
lipazin inhibitors
liver lipase inhibitor
liver lipase inhibitors
pancreatic lipase inhibitor
pancreatic lipase inhibitors
pancreatic triacylglycerol lipase inhibitor
pancreatic triacylglycerol lipase inhibitors
post-heparin plasma protamine-resistant lipase inhibitor
post-heparin plasma protamine-resistant lipase inhibitors
salt-resistant post-heparin lipase inhibitor
salt-resistant post-heparin lipase inhibitors
steapsin inhibitor
steapsin inhibitors
triacetinase inhibitor
triacetinase inhibitors
triacylglycerol ester hydrolase inhibitor
triacylglycerol ester hydrolase inhibitors
triacylglycerol lipase (EC 3.1.1.3) inhibitor
triacylglycerol lipase (EC 3.1.1.3) inhibitors
triacylglycerol lipase inhibitor
triacylglycerol lipase inhibitors
tributyrase inhibitor
tributyrase inhibitors
tributyrin esterase inhibitor
tributyrin esterase inhibitors
tributyrinase inhibitor
tributyrinase inhibitors
triglyceridase inhibitor
triglyceridase inhibitors
triglyceride hydrolase inhibitor
triglyceride hydrolase inhibitors
triglyceride lipase inhibitor
triglyceride lipase inhibitors
triolein hydrolase inhibitor
triolein hydrolase inhibitors
tween-hydrolysing esterase inhibitor
tween-hydrolyzing esterase inhibitors
EC 3.1.1.3 (triacylglycerol lipase) inhibitor
EC 3.1.1.3 (triacylglycerol lipase) inhibitors
ChEBI
EC 3.1.1.3 inhibitor
ChEBI
EC 3.1.1.3 inhibitors
ChEBI
GEH inhibitor
ChEBI
GEH inhibitors
ChEBI
PPL inhibitor
ChEBI
PPL inhibitors
ChEBI
Tween hydrolase inhibitor
ChEBI
Tween hydrolase inhibitors
ChEBI
Tweenase inhibitor
ChEBI
Tweenase inhibitors
ChEBI
Tweenesterase inhibitor
ChEBI
Tweenesterase inhibitors
ChEBI
butyrinase inhibitor
ChEBI
butyrinase inhibitors
ChEBI
cacordase inhibitor
ChEBI
cacordase inhibitors
ChEBI
capalase L inhibitor
ChEBI
capalase L inhibitors
ChEBI
glycerol ester hydrolase inhibitor
ChEBI
glycerol ester hydrolase inhibitors
ChEBI
glycerol-ester hydrolase inhibitor
ChEBI
glycerol-ester hydrolase inhibitors
ChEBI
heparin releasable hepatic lipase inhibitor
ChEBI
heparin releasable hepatic lipase inhibitors
ChEBI
hepatic lipase inhibitor
ChEBI
hepatic lipase inhibitors
ChEBI
hepatic monoacylglycerol acyltransferase inhibitor
ChEBI
hepatic monoacylglycerol acyltransferase inhibitors
ChEBI
lipase inhibitor
ChEBI
lipase inhibitors
ChEBI
lipazin inhibitor
ChEBI
lipazin inhibitors
ChEBI
liver lipase inhibitor
ChEBI
liver lipase inhibitors
ChEBI
pancreatic lipase inhibitor
ChEBI
pancreatic lipase inhibitors
ChEBI
pancreatic triacylglycerol lipase inhibitor
ChEBI
pancreatic triacylglycerol lipase inhibitors
ChEBI
post-heparin plasma protamine-resistant lipase inhibitor
ChEBI
post-heparin plasma protamine-resistant lipase inhibitors
ChEBI
salt-resistant post-heparin lipase inhibitor
ChEBI
salt-resistant post-heparin lipase inhibitors
ChEBI
steapsin inhibitor
ChEBI
steapsin inhibitors
ChEBI
triacetinase inhibitor
ChEBI
triacetinase inhibitors
ChEBI
triacylglycerol ester hydrolase inhibitor
ChEBI
triacylglycerol ester hydrolase inhibitors
ChEBI
triacylglycerol lipase (EC 3.1.1.3) inhibitor
ChEBI
triacylglycerol lipase (EC 3.1.1.3) inhibitors
ChEBI
triacylglycerol lipase inhibitor
ChEBI
triacylglycerol lipase inhibitors
ChEBI
tributyrase inhibitor
ChEBI
tributyrase inhibitors
ChEBI
tributyrin esterase inhibitor
ChEBI
tributyrin esterase inhibitors
ChEBI
tributyrinase inhibitor
ChEBI
tributyrinase inhibitors
ChEBI
triglyceridase inhibitor
ChEBI
triglyceridase inhibitors
ChEBI
triglyceride hydrolase inhibitor
ChEBI
triglyceride hydrolase inhibitors
ChEBI
triglyceride lipase inhibitor
ChEBI
triglyceride lipase inhibitors
ChEBI
triolein hydrolase inhibitor
ChEBI
triolein hydrolase inhibitors
ChEBI
tween-hydrolysing esterase inhibitor
ChEBI
tween-hydrolyzing esterase inhibitors
ChEBI
An antagonist at the vascular endothelial growth factor receptor.
VEGF receptor inhibitor
VEGF receptor inhibitors
VEGFR inhibitor
VEGFR inhibitors
vascular endothelial growth factor receptor antagonists
vascular endothelial growth factor receptor inhibitor
vascular endothelial growth factor receptor inhibitors
vascular endothelial growth factor receptor antagonist
VEGF receptor inhibitor
ChEBI
VEGF receptor inhibitors
ChEBI
VEGFR inhibitor
ChEBI
VEGFR inhibitors
ChEBI
vascular endothelial growth factor receptor antagonists
ChEBI
vascular endothelial growth factor receptor inhibitor
ChEBI
vascular endothelial growth factor receptor inhibitors
ChEBI
A carbohydrate derivative that is any derivative of a polysaccharide.
polysaccharide derivatives
polysaccharide derivative
polysaccharide derivatives
ChEBI
Substances which are added to food in order to prevent decomposition caused by microbial growth or by undesirable chemical changes.
food preservatives
food preservative
food preservatives
ChEBI
A food preservative which prevents decomposition of food by preventing the growth of fungi or bacteria. In European countries, E-numbers for permitted food preservatives are from E200 to E299, divided into sorbates (E200-209), benzoates (E210-219), sulfites (E220-229), phenols and formates (E230-239), nitrates (E240-259), acetates (E260-269), lactates (E270-279), propionates (E280-289) and others (E290-299).
antimicrobial food preservatives
antimicrobial preservative
antimicrobial preservatives
antimicrobial food preservative
antimicrobial food preservatives
ChEBI
antimicrobial preservative
ChEBI
antimicrobial preservatives
ChEBI
A compound that inhibits the action of gamma-aminobutyric acid.
GABA antagonists
gamma-aminobutyric acid receptor antagonist
gamma-aminobutyric acid receptor antagonists
GABA antagonist
GABA antagonists
ChEBI
gamma-aminobutyric acid receptor antagonist
ChEBI
gamma-aminobutyric acid receptor antagonists
ChEBI
Any dicarboxylic acid that contains four carbon atoms.
C4-dicarboxylic acids
C4-dicarboxylic acid
C4-dicarboxylic acids
ChEBI
An amino acid zwitterion arising from transfer of a proton from the carboxy to the amino group of alanine; major species at pH 7.3.
2-azaniumylpropanoate
2-ammoniopropanoate
alanine zwitterion
2-azaniumylpropanoate
IUPAC
2-ammoniopropanoate
IUPAC
Any compound used for the treatment of eye conditions or eye diseases.
ophthalmic
ophthalmic agent
ophthalmic agents
ophthalmics
ophthalmological
ophthalmologicals
ophthalmology agent
ophthalmology agents
ophthalmology drugs
ophthalmology drug
ophthalmic
ChEBI
ophthalmic agent
ChEBI
ophthalmic agents
ChEBI
ophthalmics
ChEBI
ophthalmological
ChEBI
ophthalmologicals
ChEBI
ophthalmology agent
ChEBI
ophthalmology agents
ChEBI
ophthalmology drugs
ChEBI
An N-acyl-L-alpha-amino acid anion obtained by deprotonation of any folic acid.
folate
folate anion
folate anions
folates
folate
ChEBI
folate anion
ChEBI
folate anions
ChEBI
An organophosphate oxoanion obtained by the deprotonation of the carboxy and one of the phosphate OH groups of glyphosate.
{[(hydroxyphosphinato)methyl]amino}acetate
glyphosate anion(2-)
glyphosate(2-)
{[(hydroxyphosphinato)methyl]amino}acetate
IUPAC
glyphosate anion(2-)
ChEBI
Any compound that has anti-inflammatory effects.
anti-inflammatory agents
antiinflammatory agent
antiinflammatory agents
anti-inflammatory agent
anti-inflammatory agents
ChEBI
antiinflammatory agent
ChEBI
antiinflammatory agents
ChEBI
A chemosterilant intended to sterilize insects.
insect chemosterilant
insect chemosterilants
insect sterilants
insect sterilant
insect chemosterilant
ChEBI
insect chemosterilants
ChEBI
insect sterilants
ChEBI
A ryanodine receptor modulator which activates the receptor. Ryanodine receptors (RyRs) act as selective ion channels, modulating the release of calcium. Activating the receptors causes the release of calcium, so depleting internal calcium and ultimately preventing further muscle contraction.
RyR activator
RyR activators
RyR agonist
RyR agonists
RyRs activator
RyRs agonist
ryanodine receptor activator
ryanodine receptor activators
ryanodine receptor agonist
RyR activator
ChEBI
RyR activators
ChEBI
RyR agonist
ChEBI
RyR agonists
ChEBI
RyRs activator
ChEBI
RyRs agonist
ChEBI
ryanodine receptor activator
ChEBI
ryanodine receptor activators
ChEBI
A molecule that can substitute for a normal nucleobase in nucleic acids.
base analog
base analogs
base analogue
base analogues
nucleobase analog
nucleobase analogs
nucleobase analogues
nucleobase analogue
base analog
ChEBI
base analogs
ChEBI
base analogue
ChEBI
base analogues
ChEBI
nucleobase analog
ChEBI
nucleobase analogs
ChEBI
nucleobase analogues
ChEBI
A provitamin that can be converted into vitamin A by enzymes from animal tissues.
provitamin As
provitamin A
provitamin As
ChEBI
Any monocyclic heteroarene consisting of a five-membered ring containing nitrogen. Azoles can also contain one or more other non-carbon atoms, such as nitrogen, sulfur or oxygen.
azoles
azole
azoles
ChEBI
Any substance that inhibits the process of apoptosis (programmed cell death) in multi-celled organisms.
Type I cell-death inhibitor
Type I cell-death inhibitors
Type I programmed cell-death inhibitor
Type I programmed cell-death inhibitors
apoptosis inhibitors
apoptosis inhibitor
Type I cell-death inhibitor
ChEBI
Type I cell-death inhibitors
ChEBI
Type I programmed cell-death inhibitor
ChEBI
Type I programmed cell-death inhibitors
ChEBI
apoptosis inhibitors
ChEBI
Any substance that induces the process of apoptosis (programmed cell death) in multi-celled organisms.
Type I cell-death inducer
Type I cell-death inducers
Type I programmed cell-death inducer
Type I programmed cell-death inducers
apoptosis inducers
apoptosis inducer
Type I cell-death inducer
ChEBI
Type I cell-death inducers
ChEBI
Type I programmed cell-death inducer
ChEBI
Type I programmed cell-death inducers
ChEBI
apoptosis inducers
ChEBI
A flavone C-glycoside that is luteolin attached to a disaccharide residue at position 6. It has been isolated from natural product Petrorhagia velutina and Zea mays and exhibits insecticidal and neuroprotective activities.
(6R)-2,6-anhydro-1-deoxy-5-O-(6-deoxy-alpha-D-mannopyranosyl)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-6-yl]-D-xylo-hex-3-ulose
maysin
(6R)-2,6-anhydro-1-deoxy-5-O-(6-deoxy-alpha-D-mannopyranosyl)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-6-yl]-D-xylo-hex-3-ulose
IUPAC
An EC 5.99.1.* (miscellaneous isomerase) inhibitor that interferes with the action of any of the topoisomerases (enzymes that regulate the overwinding or underwinding of DNA).
topoisomerase inhibitors
topoisomerase inhibitor
topoisomerase inhibitors
ChEBI
An antagonist at any adenosine receptor.
adenosine receptor antagonists
adenosine receptor antagonist
adenosine receptor antagonists
ChEBI
An enzyme inhibitor that inhibits the action of a transferase (EC 2.*)
EC 2 inhibitor
EC 2 inhibitors
EC 2.* (transferase) inhibitors
EC 2.* inhibitor
EC 2.* inhibitors
transferase inhibitor
transferase inhibitors
EC 2.* (transferase) inhibitor
EC 2 inhibitor
ChEBI
EC 2 inhibitors
ChEBI
EC 2.* (transferase) inhibitors
ChEBI
EC 2.* inhibitor
ChEBI
EC 2.* inhibitors
ChEBI
transferase inhibitor
ChEBI
transferase inhibitors
ChEBI
An EC 2.3.1.* (acyltransferase transferring other than amino-acyl group) inhibitor that interferes with the action of fatty acid synthase (EC 2.3.1.85), a multi-enzyme protein involved in fatty acid synthesis.
(FAS) inhibitors
EC 2.3.1.85 (fatty acid synthase) inhibitors
EC 2.3.1.85 inhibitor
EC 2.3.1.85 inhibitors
acyl-CoA:malonyl-CoA C-acyltransferase (decarboxylating, oxoacyl- and enoyl-reducing and thioester-hydrolysing) inhibitor
acyl-CoA:malonyl-CoA C-acyltransferase (decarboxylating, oxoacyl- and enoyl-reducing and thioester-hydrolysing) inhibitors
fatty acid synthase (EC 2.3.1.85) inhibitor
fatty acid synthase (EC 2.3.1.85) inhibitors
fatty acid synthase inhibitor
fatty acid synthase inhibitors
EC 2.3.1.85 (fatty acid synthase) inhibitor
(FAS) inhibitors
ChEBI
EC 2.3.1.85 (fatty acid synthase) inhibitors
ChEBI
EC 2.3.1.85 inhibitor
ChEBI
EC 2.3.1.85 inhibitors
ChEBI
acyl-CoA:malonyl-CoA C-acyltransferase (decarboxylating, oxoacyl- and enoyl-reducing and thioester-hydrolysing) inhibitor
ChEBI
acyl-CoA:malonyl-CoA C-acyltransferase (decarboxylating, oxoacyl- and enoyl-reducing and thioester-hydrolysing) inhibitors
ChEBI
fatty acid synthase (EC 2.3.1.85) inhibitor
ChEBI
fatty acid synthase (EC 2.3.1.85) inhibitors
ChEBI
fatty acid synthase inhibitor
ChEBI
fatty acid synthase inhibitors
ChEBI
Any organic molecular entity whose stucture is based on derivatives of a phenyl-substituted 1-phenylpropane possessing a C15 or C16 skeleton, or such a structure which is condensed with a C6-C3 lignan precursors. The term is a 'superclass' comprising all members of the classes of flavonoid, isoflavonoid, neoflavonoid, chalcones, dihydrochalcones, aurones, pterocarpan, coumestans, rotenoid, flavonolignan, homoflavonoid and flavonoid oligomers. Originally restricted to natural products, the term is also applied to synthetic compounds related to them.
flavonoid
flavonoids
flavonoid
ChEBI
Any molecule that consists of at least one carbon atom as part of the electrically neutral entity.
organic compound
organic compounds
organic molecules
organic molecule
organic compound
ChEBI
organic compounds
ChEBI
organic molecules
ChEBI
Any organic cation that consists of a chromenylium skeleton and its substituted derivatives thereof.
benzopyryliums
chromenyliums
benzopyryliums
ChEBI
Any polyunsaturated fatty acid that contains three double bonds.
trienoic fatty acids
trienoic fatty acid
trienoic fatty acids
ChEBI
An EC 1.11.1.* (peroxidases) inhibitor that inhibits the action of L-ascorbate peroxidase (EC 1.11.1.11).
EC 1.11.1.11 (L-ascorbate peroxidase) inhibitors
EC 1.11.1.11 inhibitor
EC 1.11.1.11 inhibitors
L-ascorbate peroxidase (EC 1.11.1.11) inhibitor
L-ascorbate peroxidase (EC 1.11.1.11) inhibitors
L-ascorbate peroxidase inhibitor
L-ascorbate peroxidase inhibitors
L-ascorbate:hydrogen-peroxide oxidoreductase inhibitor
L-ascorbate:hydrogen-peroxide oxidoreductase inhibitors
L-ascorbic acid peroxidase inhibitor
L-ascorbic acid peroxidase inhibitors
L-ascorbic acid-specific peroxidase inhibitor
L-ascorbic acid-specific peroxidase inhibitors
ascorbate peroxidase inhibitor
ascorbate peroxidase inhibitors
ascorbic acid peroxidase inhibitor
ascorbic acid peroxidase inhibitors
EC 1.11.1.11 (L-ascorbate peroxidase) inhibitor
EC 1.11.1.11 (L-ascorbate peroxidase) inhibitors
ChEBI
EC 1.11.1.11 inhibitor
ChEBI
EC 1.11.1.11 inhibitors
ChEBI
L-ascorbate peroxidase (EC 1.11.1.11) inhibitor
ChEBI
L-ascorbate peroxidase (EC 1.11.1.11) inhibitors
ChEBI
L-ascorbate peroxidase inhibitor
ChEBI
L-ascorbate peroxidase inhibitors
ChEBI
L-ascorbate:hydrogen-peroxide oxidoreductase inhibitor
ChEBI
L-ascorbate:hydrogen-peroxide oxidoreductase inhibitors
ChEBI
L-ascorbic acid peroxidase inhibitor
ChEBI
L-ascorbic acid peroxidase inhibitors
ChEBI
L-ascorbic acid-specific peroxidase inhibitor
ChEBI
L-ascorbic acid-specific peroxidase inhibitors
ChEBI
ascorbate peroxidase inhibitor
ChEBI
ascorbate peroxidase inhibitors
ChEBI
ascorbic acid peroxidase inhibitor
ChEBI
ascorbic acid peroxidase inhibitors
ChEBI
An agonist that binds to and activates abscisic acid receptors.
ABA agonist
ABA agonists
ABA receptor agonist
ABA receptor agonists
abscisic acid receptor agonists
abscisic acid receptor agonist
ABA agonist
ChEBI
ABA agonists
ChEBI
ABA receptor agonist
ChEBI
ABA receptor agonists
ChEBI
abscisic acid receptor agonists
ChEBI
An L-alpha-amino acid which is biosynthesised from erythrose 4-phosphate and phosphoenolpyruvate (i.e. phenylalanine, tyrosine, and tryptophan). A closed class.
erythrose 4-phosphate and phosphoenolpyruvate family amino acid
erythrose 4-phosphate and phosphoenolpyruvate family amino acids
erythrose 4-phosphate family amino acid
erythrose 4-phosphate family amino acids
erythrose 4-phosphate/phosphoenolpyruvate family amino acids
phosphoenolpyruvate family amino acid
phosphoenolpyruvate family amino acids
erythrose 4-phosphate/phosphoenolpyruvate family amino acid
erythrose 4-phosphate and phosphoenolpyruvate family amino acid
ChEBI
erythrose 4-phosphate and phosphoenolpyruvate family amino acids
ChEBI
erythrose 4-phosphate family amino acid
ChEBI
erythrose 4-phosphate family amino acids
ChEBI
erythrose 4-phosphate/phosphoenolpyruvate family amino acids
ChEBI
phosphoenolpyruvate family amino acid
ChEBI
phosphoenolpyruvate family amino acids
ChEBI
An antimetabolite that impairs the action of folic acids
antifolates
folic acid antagonist
folic acid antagonists
antifolate
antifolates
ChEBI
folic acid antagonist
ChEBI
folic acid antagonists
ChEBI
A compound that causes the contraction of body tissues, typically used to reduce bleeding from minor abrasions.
adstringent
adstringents
astringents
astringent
adstringent
ChEBI
adstringents
ChEBI
astringents
ChEBI
Any oligosaccharide that has a biosynthetic pathway in common with that of raffinose.
raffinose family oligosaccharides
raffinose family oligosaccharide
raffinose family oligosaccharides
ChEBI
An EC 1.11.* (oxidoreductase acting on peroxide as donors) inhibitor that interferes with the action of any of the peroxidases (EC 1.11.1.*).
EC 1.11.1 inhibitor
EC 1.11.1 inhibitors
EC 1.11.1.* (peroxidase) inhibitor
EC 1.11.1.* (peroxidase) inhibitors
EC 1.11.1.* (peroxidases) inhibitors
EC 1.11.1.* inhibitor
EC 1.11.1.* inhibitors
inhibitor of peroxidases
inhibitors of peroxidases
peroxidases inhibitors
EC 1.11.1.* (peroxidases) inhibitor
EC 1.11.1 inhibitor
ChEBI
EC 1.11.1 inhibitors
ChEBI
EC 1.11.1.* (peroxidase) inhibitor
ChEBI
EC 1.11.1.* (peroxidase) inhibitors
ChEBI
EC 1.11.1.* (peroxidases) inhibitors
ChEBI
EC 1.11.1.* inhibitor
ChEBI
EC 1.11.1.* inhibitors
ChEBI
inhibitor of peroxidases
ChEBI
inhibitors of peroxidases
ChEBI
peroxidases inhibitors
ChEBI
An enzyme inhibitor that inhibits the action of an isomerase (EC 5.*.*.*).
EC 5.* (isomerase) inhibitors
EC 5.* inhibitor
EC 5.* inhibitors
EC 5.*.*.* inhibitor
EC 5.*.*.* inhibitors
isomerase (EC 5.*) inhibitor
isomerase (EC 5.*) inhibitors
isomerase inhibitor
isomerase inhibitors
EC 5.* (isomerase) inhibitor
EC 5.* (isomerase) inhibitors
ChEBI
EC 5.* inhibitor
ChEBI
EC 5.* inhibitors
ChEBI
EC 5.*.*.* inhibitor
ChEBI
EC 5.*.*.* inhibitors
ChEBI
isomerase (EC 5.*) inhibitor
ChEBI
isomerase (EC 5.*) inhibitors
ChEBI
isomerase inhibitor
ChEBI
isomerase inhibitors
ChEBI
A ligase inhibitor that interferes with the action of a C-N bond-forming ligase (EC 6.3.*.*).
C--N bond-forming ligase inhibitor
C--N bond-forming ligase inhibitors
C-N bond-forming ligase (EC 6.3.*) inhibitor
C-N bond-forming ligase (EC 6.3.*) inhibitors
C-N bond-forming ligase inhibitor
C-N bond-forming ligase inhibitors
EC 6.3.* (C-N bond-forming ligase) inhibitorS
EC 6.3.* inhibitor
EC 6.3.* inhibitors
EC 6.3.*.* inhibitor
EC 6.3.*.* inhibitors
EC 6.3.* (C-N bond-forming ligase) inhibitor
C--N bond-forming ligase inhibitor
ChEBI
C--N bond-forming ligase inhibitors
ChEBI
C-N bond-forming ligase (EC 6.3.*) inhibitor
ChEBI
C-N bond-forming ligase (EC 6.3.*) inhibitors
ChEBI
C-N bond-forming ligase inhibitor
ChEBI
C-N bond-forming ligase inhibitors
ChEBI
EC 6.3.* (C-N bond-forming ligase) inhibitorS
ChEBI
EC 6.3.* inhibitor
ChEBI
EC 6.3.* inhibitors
ChEBI
EC 6.3.*.* inhibitor
ChEBI
EC 6.3.*.* inhibitors
ChEBI
Any enzyme inhibitor that interferes with the action of a ligase (EC 6.*.*.*). Ligases are enzymes that catalyse the joining of two molecules with concomitant hydrolysis of the diphosphate bond in ATP or a similar triphosphate.
EC 6.* (ligase) inhibitors
EC 6.* inhibitor
EC 6.* inhibitors
EC 6.*.*.* inhibitor
EC 6.*.*.* inhibitors
ligase inhibitor
ligase inhibitors
EC 6.* (ligase) inhibitor
EC 6.* (ligase) inhibitors
ChEBI
EC 6.* inhibitor
ChEBI
EC 6.* inhibitors
ChEBI
EC 6.*.*.* inhibitor
ChEBI
EC 6.*.*.* inhibitors
ChEBI
ligase inhibitor
ChEBI
ligase inhibitors
ChEBI
Any metabolite produced during a metabolic reaction in eukaryotes, the taxon that include members of the fungi, plantae and animalia kingdoms.
eukaryotic metabolites
eukaryotic metabolite
eukaryotic metabolites
ChEBI
Any eukaryotic metabolite produced during a metabolic reaction in animals that include diverse creatures from sponges, insects to mammals.
animal metabolites
animal metabolite
animal metabolites
ChEBI
Any animal metabolite produced during a metabolic reaction in mammals.
mammalian metabolites
mammalian metabolite
mammalian metabolites
ChEBI
Any member of the group of eight water-soluble vitamins originally thought to be a single compound (vitamin B) that play important roles in cell metabolism. The group comprises of vitamin B1, B2, B3, B5, B6, B7, B9, and B12 (Around 20 other compounds were once thought to be B vitamins but are no longer classified as such).
B vitamins
B-group vitamin
B-group vitamins
vitamin B
B vitamin
B vitamins
ChEBI
B-group vitamin
ChEBI
B-group vitamins
ChEBI
vitamin B
ChEBI
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
Mus musculus metabolite
Mus musculus metabolites
mouse metabolites
mouse metabolite
Mus musculus metabolite
ChEBI
Mus musculus metabolites
ChEBI
mouse metabolites
ChEBI
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae).
S. cerevisiae metabolite
S. cerevisiae metabolites
S. cerevisiae secondary metabolite
S. cerevisiae secondary metabolites
Saccharomyces cerevisiae metabolites
Saccharomyces cerevisiae secondary metabolites
baker's yeast metabolite
baker's yeast metabolites
baker's yeast secondary metabolite
baker's yeast secondary metabolites
Saccharomyces cerevisiae metabolite
S. cerevisiae metabolite
ChEBI
S. cerevisiae metabolites
ChEBI
S. cerevisiae secondary metabolite
ChEBI
S. cerevisiae secondary metabolites
ChEBI
Saccharomyces cerevisiae metabolites
ChEBI
Saccharomyces cerevisiae secondary metabolites
ChEBI
baker's yeast metabolite
ChEBI
baker's yeast metabolites
ChEBI
baker's yeast secondary metabolite
ChEBI
baker's yeast secondary metabolites
ChEBI
Any metabolite produced during a metabolic reaction in prokaryotes, the taxon that include members of domains such as the bacteria and archaea.
prokaryotic metabolites
prokaryotic metabolite
prokaryotic metabolites
ChEBI
A compound of iron and sulfate in which the ratio of iron(2+) to sulfate ions is 1:1. Various hydrates occur naturally - most commonly the heptahydrate, which loses water to form the tetrahydrate at 57degreeC and the monohydrate at 65degreeC.
iron(2+) sulfate
Fe(II)SO4
FeSO4
ferrous sulfate
ferrous sulfate (anh.)
ferrous sulfate (anhydrous)
ferrous sulfate anhydrous
iron sulfate (1:1)
iron(2+) sulfate (anh.)
iron(II) sulfate
iron(II) sulfate (1:1)
iron(2+) sulfate (anhydrous)
iron(2+) sulfate
IUPAC
Fe(II)SO4
ChEBI
FeSO4
ChEBI
ferrous sulfate
ChemIDplus
ferrous sulfate (anh.)
ChEBI
ferrous sulfate (anhydrous)
ChEBI
ferrous sulfate anhydrous
ChemIDplus
iron sulfate (1:1)
ChemIDplus
iron(2+) sulfate (anh.)
ChEBI
iron(II) sulfate
ChEBI
iron(II) sulfate (1:1)
ChemIDplus
An amino acid zwitterion obtained by transfer of a proton from the carboxy to the amino group of any aromatic amino-acid.
an aromatic amino-acid
aromatic amino-acid zwitterions
aromatic amino-acid zwitterion
an aromatic amino-acid
UniProt
aromatic amino-acid zwitterions
ChEBI
Any metabolite produced by metabolism of a xenobiotic compound.
xenobiotic metabolites
xenobiotic metabolite
xenobiotic metabolites
ChEBI
A gas in an atmosphere that absorbs and emits radiation within the thermal infrared range, so contributing to the 'greenhouse effect'.
greenhouse gases
greenhouse gas
greenhouse gases
ChEBI
A compressed gas or liquid with a boiling point lower than room temperature which to used to propel and dispense liquids such as deodorants, insecticides, paints, etc. from aerosol cans.
propellants
propellant
propellants
ChEBI
Any metabolite produced during a metabolic reaction in marine macro- and microorganisms.
marine metabolites
marine metabolite
marine metabolites
ChEBI
A nitroso compound that is any urea in which one of the nitrogens is substituted by a nitroso group
N-nitrosoureas
Any unsaturated fatty acid anion containing more than one C-C unsaturated bond. Major species at pH 7.3.
PUFA
polyunsaturated fatty acid anions
polyunsaturated fatty acid anion
PUFA
SUBMITTER
polyunsaturated fatty acid anions
ChEBI
A glycerol compound having one of three possible substituent groups - either acyl, alkyl, or alk-1-enyl - at each of the three possible positions sn-1, sn-2 or sn-3. has functional parent glycerol (CHEBI:17754), children: triglyceride (CHEBI:17855). Parent: is_a glycerolipid (CHEBI:35741)
triradylglycerols
triradylglycerol
triradylglycerols
ChEBI
Any protective agent that is able to prevent damage to the kidney.
nephroprotective agents
nephroprotective agent
nephroprotective agents
ChEBI
A transferase inhibitor inhibiting the action of transferase of a one-carbon-containing group (EC 2.1.*.*).
C1-transferase (EC 2.1.*) inhibitor
C1-transferase (EC 2.1.*) inhibitors
C1-transferase inhibitor
C1-transferase inhibitors
EC 2.1.* (C1-transferase) inhibitors
EC 2.1.* inhibitor
EC 2.1.* inhibitors
one-carbon-containing group transferase inhibitor
one-carbon-containing group transferase inhibitors
EC 2.1.* (C1-transferase) inhibitor
C1-transferase (EC 2.1.*) inhibitor
ChEBI
C1-transferase (EC 2.1.*) inhibitors
ChEBI
C1-transferase inhibitor
ChEBI
C1-transferase inhibitors
ChEBI
EC 2.1.* (C1-transferase) inhibitors
ChEBI
EC 2.1.* inhibitor
ChEBI
EC 2.1.* inhibitors
ChEBI
one-carbon-containing group transferase inhibitor
ChEBI
one-carbon-containing group transferase inhibitors
ChEBI
A transferase inhibitor that interferes with the action of an acyltransferase (EC 2.3.*.*).
EC 2.3.* (acyltransferase) inhibitors
EC 2.3.* inhibitor
EC 2.3.* inhibitors
acyltransferase inhibitor
acyltransferase inhibitors
EC 2.3.* (acyltransferase) inhibitor
EC 2.3.* (acyltransferase) inhibitors
ChEBI
EC 2.3.* inhibitor
ChEBI
EC 2.3.* inhibitors
ChEBI
acyltransferase inhibitor
ChEBI
acyltransferase inhibitors
ChEBI
A transferase inhibitor that inhibits the transfer of an alkyl (other than methyl) or aryl group (EC 2.5.1.*).
EC 2.5.1.* (non-methyl-alkyl or aryl transferase) inhibitors
EC 2.5.1.* inhibitor
EC 2.5.1.* inhibitors
alkyl/aryl (non-methyl) transferase inhibitor
alkyl/aryl (non-methyl) transferase inhibitors
non-methyl alkyl/aryl transferase (EC 2.5.1.*) inhibitor
non-methyl alkyl/aryl transferase (EC 2.5.1.*) inhibitors
non-methyl alkyl/aryl transferase inhibitor
non-methyl alkyl/aryl transferase inhibitors
non-methyl-alkyl or aryl transferase inhibitor
non-methyl-alkyl or aryl transferase inhibitors
EC 2.5.1.* (non-methyl-alkyl or aryl transferase) inhibitor
EC 2.5.1.* (non-methyl-alkyl or aryl transferase) inhibitors
ChEBI
EC 2.5.1.* inhibitor
ChEBI
EC 2.5.1.* inhibitors
ChEBI
alkyl/aryl (non-methyl) transferase inhibitor
ChEBI
alkyl/aryl (non-methyl) transferase inhibitors
ChEBI
non-methyl alkyl/aryl transferase (EC 2.5.1.*) inhibitor
ChEBI
non-methyl alkyl/aryl transferase (EC 2.5.1.*) inhibitors
ChEBI
non-methyl alkyl/aryl transferase inhibitor
ChEBI
non-methyl alkyl/aryl transferase inhibitors
ChEBI
non-methyl-alkyl or aryl transferase inhibitor
ChEBI
non-methyl-alkyl or aryl transferase inhibitors
ChEBI
A transferase inhibitor that inhibits the action of a phosphorus-containing group transferase (EC 2.7.*.*).
EC 2.7.* (P-containing group transferase) inhibitors
EC 2.7.* (phosphorus-containing group transferase) inhibitor
EC 2.7.* (phosphorus-containing group transferase) inhibitors
EC 2.7.* inhibitor
EC 2.7.* inhibitors
phosphorus-containing group transferase (EC 2.7.*) inhibitor
phosphorus-containing group transferase (EC 2.7.*) inhibitors
phosphorus-containing group transferase inhibitor
phosphorus-containing group transferase inhibitors
EC 2.7.* (P-containing group transferase) inhibitor
EC 2.7.* (P-containing group transferase) inhibitors
ChEBI
EC 2.7.* (phosphorus-containing group transferase) inhibitor
ChEBI
EC 2.7.* (phosphorus-containing group transferase) inhibitors
ChEBI
EC 2.7.* inhibitor
ChEBI
EC 2.7.* inhibitors
ChEBI
phosphorus-containing group transferase (EC 2.7.*) inhibitor
ChEBI
phosphorus-containing group transferase (EC 2.7.*) inhibitors
ChEBI
phosphorus-containing group transferase inhibitor
ChEBI
phosphorus-containing group transferase inhibitors
ChEBI
An isomerase inhibitor that interferes with the action of any member of the group of 'other isomerases' (EC 5.99.*.*).
EC 5.99.* (miscellaneous isomerases) inhibitor
EC 5.99.* (miscellaneous isomerases) inhibitors
EC 5.99.* (other isomerase) inhibitor
EC 5.99.* (other isomerase) inhibitors
EC 5.99.* (other isomerases) inhibitors
EC 5.99.* inhibitor
EC 5.99.* inhibitors
EC 5.99.* (other isomerases) inhibitor
EC 5.99.* (miscellaneous isomerases) inhibitor
ChEBI
EC 5.99.* (miscellaneous isomerases) inhibitors
ChEBI
EC 5.99.* (other isomerase) inhibitor
ChEBI
EC 5.99.* (other isomerase) inhibitors
ChEBI
EC 5.99.* (other isomerases) inhibitors
ChEBI
EC 5.99.* inhibitor
ChEBI
EC 5.99.* inhibitors
ChEBI
An enzyme inhibitor which interferes with the action of an oxidoreductase (EC 1.*.*.*).
EC 1.* (oxidoreductase) inhibitors
EC 1.* inhibitor
EC 1.* inhibitors
oxidoreductase (EC 1.*) inhibitor
oxidoreductase (EC 1.*) inhibitors
oxidoreductase inhibitor
oxidoreductase inhibitors
EC 1.* (oxidoreductase) inhibitor
EC 1.* (oxidoreductase) inhibitors
ChEBI
EC 1.* inhibitor
ChEBI
EC 1.* inhibitors
ChEBI
oxidoreductase (EC 1.*) inhibitor
ChEBI
oxidoreductase (EC 1.*) inhibitors
ChEBI
oxidoreductase inhibitor
ChEBI
oxidoreductase inhibitors
ChEBI
An oxidoreductase inhibitor which interferes with the action of an oxidoreductase acting on the CH-OH group of donors (EC 1.1.*.*).
EC 1.1.* (oxidoreductase acting on donor CH-OH group) inhibitors
EC 1.1.* inhibitor
EC 1.1.* inhibitors
inhibitor of oxidoreductase acting on CH-OH group of donor
inhibitor of oxidoreductase acting on CH-OH group of donors
inhibitors of oxidoreductase acting on CH-OH group of donor
inhibitors of oxidoreductase acting on CH-OH group of donors
oxidoreductase acting on donor CH-OH group (EC 1.1.*) inhibitor
oxidoreductase acting on donor CH-OH group (EC 1.1.*) inhibitors
oxidoreductase acting on donor CH-OH group inhibitor
oxidoreductase acting on donor CH-OH group inhibitors
EC 1.1.* (oxidoreductase acting on donor CH-OH group) inhibitor
EC 1.1.* (oxidoreductase acting on donor CH-OH group) inhibitors
ChEBI
EC 1.1.* inhibitor
ChEBI
EC 1.1.* inhibitors
ChEBI
inhibitor of oxidoreductase acting on CH-OH group of donor
ChEBI
inhibitor of oxidoreductase acting on CH-OH group of donors
ChEBI
inhibitors of oxidoreductase acting on CH-OH group of donor
ChEBI
inhibitors of oxidoreductase acting on CH-OH group of donors
ChEBI
oxidoreductase acting on donor CH-OH group (EC 1.1.*) inhibitor
ChEBI
oxidoreductase acting on donor CH-OH group (EC 1.1.*) inhibitors
ChEBI
oxidoreductase acting on donor CH-OH group inhibitor
ChEBI
oxidoreductase acting on donor CH-OH group inhibitors
ChEBI
An oxidoreductase inhibitor which interferes with the action of an oxidoreductase acting on the CH-NH group of donors (EC 1.5.*.*).
EC 1.5.* (oxidoreductase acting on donor CH-NH group) inhibitors
EC 1.5.* inhibitor
EC 1.5.* inhibitors
inhibitor of oxidoreductase acting on CH-NH group of donor
inhibitor of oxidoreductase acting on CH-NH group of donors
inhibitors of oxidoreductase acting on CH-NH group of donor
inhibitors of oxidoreductase acting on CH-NH group of donors
oxidoreductase acting on donor CH-NH group (EC 1.5.*) inhibitor
oxidoreductase acting on donor CH-NH group (EC 1.5.*) inhibitors
EC 1.5.* (oxidoreductase acting on donor CH-NH group) inhibitor
EC 1.5.* (oxidoreductase acting on donor CH-NH group) inhibitors
ChEBI
EC 1.5.* inhibitor
ChEBI
EC 1.5.* inhibitors
ChEBI
inhibitor of oxidoreductase acting on CH-NH group of donor
ChEBI
inhibitor of oxidoreductase acting on CH-NH group of donors
ChEBI
inhibitors of oxidoreductase acting on CH-NH group of donor
ChEBI
inhibitors of oxidoreductase acting on CH-NH group of donors
ChEBI
oxidoreductase acting on donor CH-NH group (EC 1.5.*) inhibitor
ChEBI
oxidoreductase acting on donor CH-NH group (EC 1.5.*) inhibitors
ChEBI
An oxidoreductase inhibitor which interferes with the action of an oxidoreductase of class EC 1.8.*.* (acting on a sulfur group of donors).
EC 1.8.* (oxidoreductase acting on sulfur group of donors) inhibitors
EC 1.8.* inhibitor
EC 1.8.* inhibitors
oxidoreductase acting on a sulfur group of donors (EC 1.8.*) inhibitor
oxidoreductase acting on a sulfur group of donors (EC 1.8.*) inhibitors
EC 1.8.* (oxidoreductase acting on sulfur group of donors) inhibitor
EC 1.8.* (oxidoreductase acting on sulfur group of donors) inhibitors
ChEBI
EC 1.8.* inhibitor
ChEBI
EC 1.8.* inhibitors
ChEBI
oxidoreductase acting on a sulfur group of donors (EC 1.8.*) inhibitor
ChEBI
oxidoreductase acting on a sulfur group of donors (EC 1.8.*) inhibitors
ChEBI
An oxidoreductase inhibitor which interferes with the action of an oxidoreductase acting on a heme group of donors (EC 1.9.*.*).
EC 1.9.* (oxidoreductase acting on a heme group of donors) inhibitor
EC 1.9.* (oxidoreductase acting on a heme group of donors) inhibitors
EC 1.9.* (oxidoreductase acting on donor heme group) inhibitors
EC 1.9.* inhibitor
EC 1.9.* inhibitors
oxidoreductase acting on a heme group of donors (EC 1.9.*) inhibitor
oxidoreductase acting on a heme group of donors (EC 1.9.*) inhibitors
EC 1.9.* (oxidoreductase acting on donor heme group) inhibitor
EC 1.9.* (oxidoreductase acting on a heme group of donors) inhibitor
ChEBI
EC 1.9.* (oxidoreductase acting on a heme group of donors) inhibitors
ChEBI
EC 1.9.* (oxidoreductase acting on donor heme group) inhibitors
ChEBI
EC 1.9.* inhibitor
ChEBI
EC 1.9.* inhibitors
ChEBI
oxidoreductase acting on a heme group of donors (EC 1.9.*) inhibitor
ChEBI
oxidoreductase acting on a heme group of donors (EC 1.9.*) inhibitors
ChEBI
An oxidoreductase inhibitor which interferes with the action of an oxidoreductase acting on peroxide as donors (EC 1.11.*.*).
EC 1.11.* (oxidoreductase acting on peroxide as donors) inhibitors
EC 1.11.* (oxidoreductases acting on peroxide as donors) inhibitor
EC 1.11.* (oxidoreductases acting on peroxide as donors) inhibitors
EC 1.11.* inhibitor
EC 1.11.* inhibitors
oxidoreductase acting on peroxide as donors (EC 1.11.*) inhibitor
oxidoreductase acting on peroxide as donors (EC 1.11.*) inhibitors
oxidoreductases acting on peroxide as donors (EC 1.11.*) inhibitor
oxidoreductases acting on peroxide as donors (EC 1.11.*) inhibitors
EC 1.11.* (oxidoreductase acting on peroxide as donors) inhibitor
EC 1.11.* (oxidoreductase acting on peroxide as donors) inhibitors
ChEBI
EC 1.11.* (oxidoreductases acting on peroxide as donors) inhibitor
ChEBI
EC 1.11.* (oxidoreductases acting on peroxide as donors) inhibitors
ChEBI
EC 1.11.* inhibitor
ChEBI
EC 1.11.* inhibitors
ChEBI
oxidoreductase acting on peroxide as donors (EC 1.11.*) inhibitor
ChEBI
oxidoreductase acting on peroxide as donors (EC 1.11.*) inhibitors
ChEBI
oxidoreductases acting on peroxide as donors (EC 1.11.*) inhibitor
ChEBI
oxidoreductases acting on peroxide as donors (EC 1.11.*) inhibitors
ChEBI
An oxidoreductase inhibitor which interferes with the action of an oxidoreductase acting on single donors with incorporation of molecular oxygen (oxygenases), EC 1.13.*.*.
EC 1.13.* [oxidoreductase acting on single donors with incorporation of molecular oxygen (oxygenases)] inhibitors
EC 1.13.* inhibitor
EC 1.13.* inhibitors
oxidoreductase acting on single donors with incorporation of molecular oxygen (oxygenases) (EC 1.13.*) inhibitor
oxidoreductase acting on single donors with incorporation of molecular oxygen (oxygenases) (EC 1.13.*) inhibitors
oxidoreductase acting on single donors with incorporation of molecular oxygen (oxygenases) inhibitor
oxidoreductase acting on single donors with incorporation of molecular oxygen (oxygenases) inhibitors
EC 1.13.* [oxidoreductase acting on single donors with incorporation of molecular oxygen (oxygenases)] inhibitor
EC 1.13.* [oxidoreductase acting on single donors with incorporation of molecular oxygen (oxygenases)] inhibitors
ChEBI
EC 1.13.* inhibitor
ChEBI
EC 1.13.* inhibitors
ChEBI
oxidoreductase acting on single donors with incorporation of molecular oxygen (oxygenases) (EC 1.13.*) inhibitor
ChEBI
oxidoreductase acting on single donors with incorporation of molecular oxygen (oxygenases) (EC 1.13.*) inhibitors
ChEBI
oxidoreductase acting on single donors with incorporation of molecular oxygen (oxygenases) inhibitor
ChEBI
oxidoreductase acting on single donors with incorporation of molecular oxygen (oxygenases) inhibitors
ChEBI
Any enzyme inhibitor that interferes with the action of a hydrolase (EC 3.*.*.*).
EC 3.* (hydrolase) inhibitors
EC 3.* inhibitor
EC 3.* inhibitors
EC 3.*.*.* inhibitor
EC 3.*.*.* inhibitors
hydrolase (EC 3.*) inhibitor
hydrolase (EC 3.*) inhibitors
hydrolase inhibitor
hydrolase inhibitors
EC 3.* (hydrolase) inhibitor
EC 3.* (hydrolase) inhibitors
ChEBI
EC 3.* inhibitor
ChEBI
EC 3.* inhibitors
ChEBI
EC 3.*.*.* inhibitor
ChEBI
EC 3.*.*.* inhibitors
ChEBI
hydrolase (EC 3.*) inhibitor
ChEBI
hydrolase (EC 3.*) inhibitors
ChEBI
hydrolase inhibitor
ChEBI
hydrolase inhibitors
ChEBI
A hydrolase inhibitor that interferes with the action of any ester hydrolase (EC 3.1.*.*).
EC 3.1.* (ester hydrolase) inhibitors
EC 3.1.* inhibitor
EC 3.1.* inhibitors
ester hydrolase (EC 3.1.*) inhibitor
ester hydrolase (EC 3.1.*) inhibitors
ester hydrolase inhibitor
ester hydrolase inhibitors
EC 3.1.* (ester hydrolase) inhibitor
EC 3.1.* (ester hydrolase) inhibitors
ChEBI
EC 3.1.* inhibitor
ChEBI
EC 3.1.* inhibitors
ChEBI
ester hydrolase (EC 3.1.*) inhibitor
ChEBI
ester hydrolase (EC 3.1.*) inhibitors
ChEBI
ester hydrolase inhibitor
ChEBI
ester hydrolase inhibitors
ChEBI
Any hydrolase inhibitor that interferes with the action of a hydrolase acting on C-N bonds, other than peptide bonds (EC 3.5.*.*).
EC 3.5.* (hydrolase acting on non-peptide C-N bond) inhibitor
EC 3.5.* (hydrolase acting on non-peptide C-N bond) inhibitors
EC 3.5.* (hydrolases acting on C-N bonds, other than peptide bonds) inhibitor
EC 3.5.* (hydrolases acting on C-N bonds, other than peptide bonds) inhibitors
EC 3.5.* (hydrolases acting on non-peptide C-N bonds) inhibitors
EC 3.5.* inhibitor
EC 3.5.* inhibitors
EC 3.5.* (hydrolases acting on non-peptide C-N bonds) inhibitor
EC 3.5.* (hydrolase acting on non-peptide C-N bond) inhibitor
ChEBI
EC 3.5.* (hydrolase acting on non-peptide C-N bond) inhibitors
ChEBI
EC 3.5.* (hydrolases acting on C-N bonds, other than peptide bonds) inhibitor
ChEBI
EC 3.5.* (hydrolases acting on C-N bonds, other than peptide bonds) inhibitors
ChEBI
EC 3.5.* (hydrolases acting on non-peptide C-N bonds) inhibitors
ChEBI
EC 3.5.* inhibitor
ChEBI
EC 3.5.* inhibitors
ChEBI
An EC 3.1.* (ester hydrolase) inhibitor that interferes with the action of a carboxylic ester hydrolase (EC 3.1.1.*).
EC 3.1.1.* (carboxylic ester hydrolase) inhibitors
EC 3.1.1.* inhibitor
EC 3.1.1.* inhibitors
carboxylic ester hydrolase (EC 3.1.1.*) inhibitor
carboxylic ester hydrolase (EC 3.1.1.*) inhibitors
EC 3.1.1.* (carboxylic ester hydrolase) inhibitor
EC 3.1.1.* (carboxylic ester hydrolase) inhibitors
ChEBI
EC 3.1.1.* inhibitor
ChEBI
EC 3.1.1.* inhibitors
ChEBI
carboxylic ester hydrolase (EC 3.1.1.*) inhibitor
ChEBI
carboxylic ester hydrolase (EC 3.1.1.*) inhibitors
ChEBI
An EC 3.1.* (ester hydrolase) inhibitor that interferes with the action of any phosphoric monoester hydrolase (EC 3.1.3.*).
EC 3.1.3.* (phosphoric monoester hydrolase) inhibitors
EC 3.1.3.* inhibitor
EC 3.1.3.* inhibitors
inhibitor of phosphoric monoester hydrolase
inhibitor of phosphoric monoester hydrolase (EC 3.1.3.*)
inhibitors of phosphoric monoester hydrolase
inhibitors of phosphoric monoester hydrolase (EC 3.1.3.*)
phosphoric monoester hydrolase (EC 3.1.3.*) inhibitor
phosphoric monoester hydrolase (EC 3.1.3.*) inhibitors
phosphoric monoester hydrolase inhibitor
phosphoric monoester hydrolase inhibitors
EC 3.1.3.* (phosphoric monoester hydrolase) inhibitor
EC 3.1.3.* (phosphoric monoester hydrolase) inhibitors
ChEBI
EC 3.1.3.* inhibitor
ChEBI
EC 3.1.3.* inhibitors
ChEBI
inhibitor of phosphoric monoester hydrolase
ChEBI
inhibitor of phosphoric monoester hydrolase (EC 3.1.3.*)
ChEBI
inhibitors of phosphoric monoester hydrolase
ChEBI
inhibitors of phosphoric monoester hydrolase (EC 3.1.3.*)
ChEBI
phosphoric monoester hydrolase (EC 3.1.3.*) inhibitor
ChEBI
phosphoric monoester hydrolase (EC 3.1.3.*) inhibitors
ChEBI
phosphoric monoester hydrolase inhibitor
ChEBI
phosphoric monoester hydrolase inhibitors
ChEBI
An EC 3.5.* (hydrolases acting on non-peptide C-N bonds) inhibitor that interferes with the action of any non-peptide linear amide C-N hydrolase (EC 3.5.1.*).
EC 3.5.1.* (non-peptide linear amide C-N hydrolase) inhibitors
EC 3.5.1.* inhibitor
EC 3.5.1.* inhibitors
non-peptide linear amide C-N hydrolase (EC 3.5.1.*) inhibitor
non-peptide linear amide C-N hydrolase (EC 3.5.1.*) inhibitors
EC 3.5.1.* (non-peptide linear amide C-N hydrolase) inhibitor
EC 3.5.1.* (non-peptide linear amide C-N hydrolase) inhibitors
ChEBI
EC 3.5.1.* inhibitor
ChEBI
EC 3.5.1.* inhibitors
ChEBI
non-peptide linear amide C-N hydrolase (EC 3.5.1.*) inhibitor
ChEBI
non-peptide linear amide C-N hydrolase (EC 3.5.1.*) inhibitors
ChEBI
An EC 2.7.* (P-containing group transferase) inhibitor that interferes with the action of any protein-serine/threonine kinase (EC 2.7.11.*).
EC 2.7.11.* (protein-serine/threonine kinase) inhibitors
EC 2.7.11.* inhibitor
EC 2.7.11.* inhibitors
protein-serine/threonine kinase (EC 2.7.11.*) inhibitor
protein-serine/threonine kinase (EC 2.7.11.*) inhibitors
protein-serine/threonine kinase inhibitor
protein-serine/threonine kinase inhibitors
EC 2.7.11.* (protein-serine/threonine kinase) inhibitor
EC 2.7.11.* (protein-serine/threonine kinase) inhibitors
ChEBI
EC 2.7.11.* inhibitor
ChEBI
EC 2.7.11.* inhibitors
ChEBI
protein-serine/threonine kinase (EC 2.7.11.*) inhibitor
ChEBI
protein-serine/threonine kinase (EC 2.7.11.*) inhibitors
ChEBI
protein-serine/threonine kinase inhibitor
ChEBI
protein-serine/threonine kinase inhibitors
ChEBI
An EC 6.3.* (C-N bond-forming ligase) inhibitor that interferes with the action of any acid-ammonia (or amine) ligase (EC 6.3.1.*).
EC 6.3.1.* (acid-ammonia/amine ligase) inhibitors
EC 6.3.1.* inhibitor
EC 6.3.1.* inhibitors
acid-ammonia (or amine) ligase inhibitor
acid-ammonia (or amine) ligase inhibitors
EC 6.3.1.* (acid-ammonia/amine ligase) inhibitor
EC 6.3.1.* (acid-ammonia/amine ligase) inhibitors
ChEBI
EC 6.3.1.* inhibitor
ChEBI
EC 6.3.1.* inhibitors
ChEBI
acid-ammonia (or amine) ligase inhibitor
ChEBI
acid-ammonia (or amine) ligase inhibitors
ChEBI
An EC 5.99.* (other isomerases) inhibitor that interferes with the activity of any enzyme in the EC 5.99.1.* class.
EC 5.99.1.* (miscellaneous isomerase) inhibitors
EC 5.99.1.* inhibitor
EC 5.99.1.* inhibitors
EC 5.99.1.* (miscellaneous isomerase) inhibitor
EC 5.99.1.* (miscellaneous isomerase) inhibitors
ChEBI
EC 5.99.1.* inhibitor
ChEBI
EC 5.99.1.* inhibitors
ChEBI
An EC 2.5.* (transferase) inhibitor that inhibits the action of any transferase that transfers an alkyl (other than methyl) or aryl group (EC 2.5.*).
EC 2.5.* (non-methyl-alkyl or aryl transferase) inhibitors
EC 2.5.* inhibitor
EC 2.5.* inhibitors
non-methyl-alkyl or aryl transferase (EC 2.5.*) inhibitor
non-methyl-alkyl or aryl transferase (EC 2.5.*) inhibitors
EC 2.5.* (non-methyl-alkyl or aryl transferase) inhibitor
EC 2.5.* (non-methyl-alkyl or aryl transferase) inhibitors
ChEBI
EC 2.5.* inhibitor
ChEBI
EC 2.5.* inhibitors
ChEBI
non-methyl-alkyl or aryl transferase (EC 2.5.*) inhibitor
ChEBI
non-methyl-alkyl or aryl transferase (EC 2.5.*) inhibitors
ChEBI
An EC 1.1.* (oxidoreductase acting on donor CH-OH group) inhibitor that uses NAD(+) or NADP(+) as acceptor (EC 1.1.1.*).
EC 1.1.1.* (oxidoreductase acting on donor CH-OH group, NAD(+) or NADP(+)acceptor) inhibitors
EC 1.1.1.* inhibitor
EC 1.1.1.* inhibitors
oxidoreductase acting on donor CH-OH group, NAD(+) or NADP(+) acceptor (EC 1.1.1.*) inhibitor
oxidoreductase acting on donor CH-OH group, NAD(+) or NADP(+) acceptor (EC 1.1.1.*) inhibitors
EC 1.1.1.* (oxidoreductase acting on donor CH-OH group, NAD(+) or NADP(+) acceptor) inhibitor
EC 1.1.1.* (oxidoreductase acting on donor CH-OH group, NAD(+) or NADP(+)acceptor) inhibitors
ChEBI
EC 1.1.1.* inhibitor
ChEBI
EC 1.1.1.* inhibitors
ChEBI
oxidoreductase acting on donor CH-OH group, NAD(+) or NADP(+) acceptor (EC 1.1.1.*) inhibitor
ChEBI
oxidoreductase acting on donor CH-OH group, NAD(+) or NADP(+) acceptor (EC 1.1.1.*) inhibitors
ChEBI
An EC 1.13.* [oxidoreductase acting on single donors with incorporation of molecular oxygen (oxygenases)] inhibitor that inhibits the action of any oxidoreductase incorporating 2 atoms of oxygen (EC 1.13.11.*).
EC 1.13.11.* (oxidoreductase acting on single donors and incorporating 2 O atoms) inhibitors
EC 1.13.11.* (oxidoreductase acting on single donors and incorporating 2 atoms of oxygen) inhibitor
EC 1.13.11.* (oxidoreductase acting on single donors and incorporating 2 atoms of oxygen) inhibitors
EC 1.13.11.* inhibitor
EC 1.13.11.* inhibitors
oxidoreductase acting on single donors and incorporating 2 atoms of oxygen (EC 1.13.11.*) inhibitor
oxidoreductase acting on single donors and incorporating 2 atoms of oxygen (EC 1.13.11.*) inhibitors
EC 1.13.11.* (oxidoreductase acting on single donors and incorporating 2 O atoms) inhibitor
EC 1.13.11.* (oxidoreductase acting on single donors and incorporating 2 O atoms) inhibitors
ChEBI
EC 1.13.11.* (oxidoreductase acting on single donors and incorporating 2 atoms of oxygen) inhibitor
ChEBI
EC 1.13.11.* (oxidoreductase acting on single donors and incorporating 2 atoms of oxygen) inhibitors
ChEBI
EC 1.13.11.* inhibitor
ChEBI
EC 1.13.11.* inhibitors
ChEBI
oxidoreductase acting on single donors and incorporating 2 atoms of oxygen (EC 1.13.11.*) inhibitor
ChEBI
oxidoreductase acting on single donors and incorporating 2 atoms of oxygen (EC 1.13.11.*) inhibitors
ChEBI
An EC 1.5.* (oxidoreductase acting on donor CH-NH group) inhibitor that interferes with the action of any such enzyme using NAD(+) or NADP(+) as acceptor (EC 1.5.1.*).
EC 1.5.1.* (oxidoreductase acting on donor CH-NH group, NAD(+) or NADP(+) as acceptor) inhibitors
EC 1.5.1.* inhibitor
EC 1.5.1.* inhibitors
oxidoreductase acting on donor CH-NH group, NAD(+) or NADP(+) as acceptor (EC 1.5.1.*) inhibitor
oxidoreductase acting on donor CH-NH group, NAD(+) or NADP(+) as acceptor (EC 1.5.1.*) inhibitors
EC 1.5.1.* (oxidoreductase acting on donor CH-NH group, NAD(+) or NADP(+) as acceptor) inhibitor
EC 1.5.1.* (oxidoreductase acting on donor CH-NH group, NAD(+) or NADP(+) as acceptor) inhibitors
ChEBI
EC 1.5.1.* inhibitor
ChEBI
EC 1.5.1.* inhibitors
ChEBI
oxidoreductase acting on donor CH-NH group, NAD(+) or NADP(+) as acceptor (EC 1.5.1.*) inhibitor
ChEBI
oxidoreductase acting on donor CH-NH group, NAD(+) or NADP(+) as acceptor (EC 1.5.1.*) inhibitors
ChEBI
An EC 1.8.* (oxidoreductase acting on sulfur group of donors) inhibitor that interferes with the action of any such enzyme using NAD(+) or NADP(+) as acceptor (EC 1.8.1.*).
EC 1.8.1.* (oxidoreductase acting on sulfur group of donors, NAD(+) or NADP(+) as acceptor) inhibitors
EC 1.8.1.* inhibitor
EC 1.8.1.* inhibitors
oxidoreductase acting on sulfur group of donors, NAD(+) or NADP(+) as acceptor (EC 1.8.1.*) inhibitor
oxidoreductase acting on sulfur group of donors, NAD(+) or NADP(+) as acceptor (EC 1.8.1.*) inhibitors
EC 1.8.1.* (oxidoreductase acting on sulfur group of donors, NAD(+) or NADP(+) as acceptor) inhibitor
EC 1.8.1.* (oxidoreductase acting on sulfur group of donors, NAD(+) or NADP(+) as acceptor) inhibitors
ChEBI
EC 1.8.1.* inhibitor
ChEBI
EC 1.8.1.* inhibitors
ChEBI
oxidoreductase acting on sulfur group of donors, NAD(+) or NADP(+) as acceptor (EC 1.8.1.*) inhibitor
ChEBI
oxidoreductase acting on sulfur group of donors, NAD(+) or NADP(+) as acceptor (EC 1.8.1.*) inhibitors
ChEBI
An EC 1.9.* (oxidoreductase acting on donor heme group) inhibitor that interferes with the action of any such enzyme using oxygen as acceptor (EC 1.9.3.*).
EC 1.9.3.* (oxidoreductase acting on donor heme group, oxygen as acceptor) inhibitors
EC 1.9.3.* inhibitor
EC 1.9.3.* inhibitors
oxidoreductase acting on donor heme group, oxygen as acceptor (EC 1.9.3.*) inhibitor
oxidoreductase acting on donor heme group, oxygen as acceptor (EC 1.9.3.*) inhibitors
EC 1.9.3.* (oxidoreductase acting on donor heme group, oxygen as acceptor) inhibitor
EC 1.9.3.* (oxidoreductase acting on donor heme group, oxygen as acceptor) inhibitors
ChEBI
EC 1.9.3.* inhibitor
ChEBI
EC 1.9.3.* inhibitors
ChEBI
oxidoreductase acting on donor heme group, oxygen as acceptor (EC 1.9.3.*) inhibitor
ChEBI
oxidoreductase acting on donor heme group, oxygen as acceptor (EC 1.9.3.*) inhibitors
ChEBI
An EC 2.1.* (C1-transferase) inhibitor that interferes with the action of any hydroxymethyl-, formyl- and related transferase (EC 2.1.2.*).
EC 2.1.2.* (hydroxymethyl-, formyl- and related transferases) inhibitors
EC 2.1.2.* inhibitor
EC 2.1.2.* inhibitors
hydroxymethyl-, formyl- and related transferases (EC 2.1.2.*) inhibitor
hydroxymethyl-, formyl- and related transferases (EC 2.1.2.*) inhibitors
EC 2.1.2.* (hydroxymethyl-, formyl- and related transferases) inhibitor
EC 2.1.2.* (hydroxymethyl-, formyl- and related transferases) inhibitors
ChEBI
EC 2.1.2.* inhibitor
ChEBI
EC 2.1.2.* inhibitors
ChEBI
hydroxymethyl-, formyl- and related transferases (EC 2.1.2.*) inhibitor
ChEBI
hydroxymethyl-, formyl- and related transferases (EC 2.1.2.*) inhibitors
ChEBI
An EC 2.3.* (acyltransferase) inhibitor that inhibits the action of any acyltransferase transferring groups other than amino-acyl groups (EC 2.3.1.*).
EC 2.3.1.* (acyltransferase transferring other than amino-acyl group) inhibitors
EC 2.3.1.* inhibitor
EC 2.3.1.* inhibitors
acyltransferase transferring other than amino-acyl group EC 2.3.1.* inhibitor
acyltransferase transferring other than amino-acyl group EC 2.3.1.* inhibitors
EC 2.3.1.* (acyltransferase transferring other than amino-acyl group) inhibitor
EC 2.3.1.* (acyltransferase transferring other than amino-acyl group) inhibitors
ChEBI
EC 2.3.1.* inhibitor
ChEBI
EC 2.3.1.* inhibitors
ChEBI
acyltransferase transferring other than amino-acyl group EC 2.3.1.* inhibitor
ChEBI
acyltransferase transferring other than amino-acyl group EC 2.3.1.* inhibitors
ChEBI
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
plant metabolites
plant secondary metabolites
plant metabolite
plant metabolites
ChEBI
plant secondary metabolites
ChEBI
An enzyme inhibitor that interferes with one or more steps in a metabolic pathway.
metabolic pathway inhibitor
metabolic pathway inhibitors
pathway inhibitors
pathway inhibitor
metabolic pathway inhibitor
ChEBI
metabolic pathway inhibitors
ChEBI
pathway inhibitors
ChEBI
Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
fungal metabolites
fungal metabolite
fungal metabolites
ChEBI
Any fungal metabolite produced during a metabolic reaction in the mould, Aspergillus.
Aspergillus metabolites
Aspergillus metabolite
Aspergillus metabolites
ChEBI
Any human metabolite produced by metabolism of a xenobiotic compound in humans.
human xenobiotic metabolites
human xenobiotic metabolite
human xenobiotic metabolites
ChEBI
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
bacterial metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
E.coli metabolite
E.coli metabolites
Escherichia coli metabolites
Escherichia coli metabolite
E.coli metabolite
ChEBI
E.coli metabolites
ChEBI
Escherichia coli metabolites
ChEBI
A food additive that imparts colour to food. In European countries, E-numbers for permitted food colours are from E 100 to E 199, divided into yellows (E 100-109), oranges (E 110-119), reds (E 120-129), blues and violets (E 130-139), greens (E 140-149), browns and blacks (E 150-159), and others (E 160-199).
food coloring
food colorings
food colourings
food colouring
food coloring
ChEBI
food colorings
ChEBI
food colourings
ChEBI
Any protective agent that is able to prevent damage to the heart.
cardioprotective agents
cardioprotective agent
cardioprotective agents
ChEBI
An EC 1.8.1.* (oxidoreductase acting on sulfur group of donors, NAD+ or NADP+ as acceptor) inhibitor that interferes with the action of trypanothione-disulfide reductase (EC 1.8.1.12).
EC 1.8.1.12 (trypanothione-disulfide reductase) inhibitors
EC 1.8.1.12 inhibitor
EC 1.8.1.12 inhibitors
N(1),N(8)-bis(glutathionyl)spermidine reductase inhibitor
N(1),N(8)-bis(glutathionyl)spermidine reductase inhibitors
NADPH2:trypanothione oxidoreductase inhibitor
NADPH2:trypanothione oxidoreductase inhibitors
NADPH:trypanothione oxidoreductase inhibitor
NADPH:trypanothione oxidoreductase inhibitors
trypanothione reductase inhibitor
trypanothione reductase inhibitors
trypanothione-disulfide reductase (EC 1.8.1.12) inhibitor
trypanothione-disulfide reductase (EC 1.8.1.12) inhibitors
trypanothione:NADP(+) oxidoreductase inhibitor
trypanothione:NADP(+) oxidoreductase inhibitors
EC 1.8.1.12 (trypanothione-disulfide reductase) inhibitor
EC 1.8.1.12 (trypanothione-disulfide reductase) inhibitors
ChEBI
EC 1.8.1.12 inhibitor
ChEBI
EC 1.8.1.12 inhibitors
ChEBI
N(1),N(8)-bis(glutathionyl)spermidine reductase inhibitor
ChEBI
N(1),N(8)-bis(glutathionyl)spermidine reductase inhibitors
ChEBI
NADPH2:trypanothione oxidoreductase inhibitor
ChEBI
NADPH2:trypanothione oxidoreductase inhibitors
ChEBI
NADPH:trypanothione oxidoreductase inhibitor
ChEBI
NADPH:trypanothione oxidoreductase inhibitors
ChEBI
trypanothione reductase inhibitor
ChEBI
trypanothione reductase inhibitors
ChEBI
trypanothione-disulfide reductase (EC 1.8.1.12) inhibitor
ChEBI
trypanothione-disulfide reductase (EC 1.8.1.12) inhibitors
ChEBI
trypanothione:NADP(+) oxidoreductase inhibitor
ChEBI
trypanothione:NADP(+) oxidoreductase inhibitors
ChEBI
An EC 1.1.1.* (oxidoreductase acting on donor CH-OH group, NAD(+) or NADP(+) acceptor) inhibitor that interferes with the action of shikimate dehydrogenase (EC 1.1.1.25).
5-dehydroshikimate reductase inhibitor
5-dehydroshikimate reductase inhibitors
5-dehydroshikimic reductase inhibitor
5-dehydroshikimic reductase inhibitors
AroE inhibitor
AroE inhibitors
DHS reductase inhibitor
DHS reductase inhibitors
EC 1.1.1.25 (shikimate dehydrogenase) inhibitors
EC 1.1.1.25 inhibitor
EC 1.1.1.25 inhibitors
dehydroshikimic reductase inhibitor
dehydroshikimic reductase inhibitors
shikimate 5-dehydrogenase inhibitor
shikimate 5-dehydrogenase inhibitors
shikimate dehydrogenase (EC 1.1.1.25) inhibitor
shikimate dehydrogenase (EC 1.1.1.25) inhibitors
shikimate dehydrogenase inhibitor
shikimate dehydrogenase inhibitors
shikimate oxidoreductase inhibitor
shikimate oxidoreductase inhibitors
shikimate:NADP(+) 3-oxidoreductase inhibitor
shikimate:NADP(+) 3-oxidoreductase inhibitors
shikimate:NADP(+) 5-oxidoreductase inhibitor
shikimate:NADP(+) 5-oxidoreductase inhibitors
shikimate:NADP(+) oxidoreductase inhibitor
shikimate:NADP(+) oxidoreductase inhibitors
EC 1.1.1.25 (shikimate dehydrogenase) inhibitor
5-dehydroshikimate reductase inhibitor
ChEBI
5-dehydroshikimate reductase inhibitors
ChEBI
5-dehydroshikimic reductase inhibitor
ChEBI
5-dehydroshikimic reductase inhibitors
ChEBI
AroE inhibitor
ChEBI
AroE inhibitors
ChEBI
DHS reductase inhibitor
ChEBI
DHS reductase inhibitors
ChEBI
EC 1.1.1.25 (shikimate dehydrogenase) inhibitors
ChEBI
EC 1.1.1.25 inhibitor
ChEBI
EC 1.1.1.25 inhibitors
ChEBI
dehydroshikimic reductase inhibitor
ChEBI
dehydroshikimic reductase inhibitors
ChEBI
shikimate 5-dehydrogenase inhibitor
ChEBI
shikimate 5-dehydrogenase inhibitors
ChEBI
shikimate dehydrogenase (EC 1.1.1.25) inhibitor
ChEBI
shikimate dehydrogenase (EC 1.1.1.25) inhibitors
ChEBI
shikimate dehydrogenase inhibitor
ChEBI
shikimate dehydrogenase inhibitors
ChEBI
shikimate oxidoreductase inhibitor
ChEBI
shikimate oxidoreductase inhibitors
ChEBI
shikimate:NADP(+) 3-oxidoreductase inhibitor
ChEBI
shikimate:NADP(+) 3-oxidoreductase inhibitors
ChEBI
shikimate:NADP(+) 5-oxidoreductase inhibitor
ChEBI
shikimate:NADP(+) 5-oxidoreductase inhibitors
ChEBI
shikimate:NADP(+) oxidoreductase inhibitor
ChEBI
shikimate:NADP(+) oxidoreductase inhibitors
ChEBI
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
H. sapiens metabolite
H. sapiens metabolites
Homo sapiens metabolite
Homo sapiens metabolites
human metabolite
H. sapiens metabolite
ChEBI
H. sapiens metabolites
ChEBI
Homo sapiens metabolite
ChEBI
Homo sapiens metabolites
ChEBI
An EC 3.5.1.* (non-peptide linear amide C-N hydrolase) inhibitor that interferes with the action of amidase (EC 3.5.1.4).
EC 3.5.1.4 (amidase) inhibitors
EC 3.5.1.4 inhibitor
EC 3.5.1.4 inhibitors
N-acetylaminohydrolase inhibitor
N-acetylaminohydrolase inhibitors
acylamidase inhibitor
acylamidase inhibitors
acylamide amidohydrolase inhibitor
acylamide amidohydrolase inhibitors
amidase (EC 3.5.1.4) inhibitor
amidase (EC 3.5.1.4) inhibitors
amidase inhibitor
amidase inhibitors
amidohydrolase inhibitor
amidohydrolase inhibitors
deaminase inhibitor
deaminase inhibitors
fatty acylamidase inhibitor
fatty acylamidase inhibitors
EC 3.5.1.4 (amidase) inhibitor
EC 3.5.1.4 (amidase) inhibitors
ChEBI
EC 3.5.1.4 inhibitor
ChEBI
EC 3.5.1.4 inhibitors
ChEBI
N-acetylaminohydrolase inhibitor
ChEBI
N-acetylaminohydrolase inhibitors
ChEBI
acylamidase inhibitor
ChEBI
acylamidase inhibitors
ChEBI
acylamide amidohydrolase inhibitor
ChEBI
acylamide amidohydrolase inhibitors
ChEBI
amidase (EC 3.5.1.4) inhibitor
ChEBI
amidase (EC 3.5.1.4) inhibitors
ChEBI
amidase inhibitor
ChEBI
amidase inhibitors
ChEBI
amidohydrolase inhibitor
ChEBI
amidohydrolase inhibitors
ChEBI
deaminase inhibitor
ChEBI
deaminase inhibitors
ChEBI
fatty acylamidase inhibitor
ChEBI
fatty acylamidase inhibitors
ChEBI
A substance added to powdered or granulated materials in order to prevent the formation of lumps and so facilitate its packaging or transport.
anti-caking agent
anti-caking agents
anticaking agents
anticaking agent
anti-caking agent
ChEBI
anti-caking agents
ChEBI
anticaking agents
ChEBI
An anticaking agent that is used to reduced the tendency of particles of food to adhere to one another.
food anticaking agent
food anti-caking agent
food anti-caking agents
food anticaking agent
food anticaking agent
ChEBI
food anti-caking agent
ChEBI
food anti-caking agents
ChEBI
A food additive that is used to preserve the structure of food.
food stabilisers
food stabilizer
food stabilizers
stabiliser
stabilisers
stabilizer
stabilizers
food stabiliser
food stabilisers
ChEBI
food stabilizer
ChEBI
food stabilizers
ChEBI
stabiliser
ChEBI
stabilisers
ChEBI
stabilizer
ChEBI
stabilizers
ChEBI
A compound that is used to keep a substance moist.
humectants
humectant
humectants
ChEBI
A humectant that is used as a food additive to prevent foodstuffs from drying out.
food humectants
food humectant
food humectants
ChEBI
A food additive that is used to increase the viscosity of foodstuffs.
food thickening agents
thickening agent
thickening agents
food thickening agent
food thickening agents
ChEBI
thickening agent
ChEBI
thickening agents
ChEBI
A food additive that is a (generally inert) gas which is used to envelop foodstuffs during packing and so protect them from unwanted chemical reactions such as food spoilage or oxidation during subsequent transport and storage. The term includes propellant gases, used to expel foods from a container.
food packaging gases
food packaging gas
food packaging gases
ChEBI
A food additive that contributes to the bulk of a food without significantly contributing to its available energy value.
filler
fillers
food bulking agents
food bulking agent
filler
ChEBI
fillers
ChEBI
food bulking agents
ChEBI
A propellant that is used to expel foods from an aerosol container.
food propellants
food propellant
food propellants
ChEBI
A fatty acid anion containing 18 carbons and one double bond. Formed by deprotonation of the carboxylic acid group. Major species at pH 7.3.
octadecenoate
Any saturated fatty acid anion containing 3 carbons. Formed by deprotonation of the carboxylic acid moiety. Major species at pH 7.3.
fatty acid 3:0
fatty acid anion 3:0
fatty acid 3:0
UniProt
Any saturated fatty acid anion containing 18 carbons. Formed by deprotonation of the carboxylic acid moiety. Major species at pH 7.3.
fatty acid 18:0
fatty acid anion 18:0
fatty acid 18:0
UniProt
A physiological role played by any substance that is distributed in foodstuffs. It includes materials derived from plants or animals, such as vitamins or minerals, as well as environmental contaminants.
dietary component
dietary components
food components
food component
dietary component
ChEBI
dietary components
ChEBI
food components
ChEBI
Any minor or unwanted substance introduced into the environment that can have undesired effects.
environmental contaminants
environmental contaminant
environmental contaminants
ChEBI
A substance used in a thermodynamic heat pump cycle or refrigeration cycle that undergoes a phase change from a gas to a liquid and back. Refrigerants are used in air-conditioning systems and freezers or refrigerators and are assigned a "R" number (by ASHRAE - formerly the American Society of Heating, Refrigerating and Air Conditioning Engineers), which is determined systematically according to their molecular structure.
refrigerants
refrigerant
refrigerants
ChEBI
Any EC 3.1.1.* (carboxylic ester hydrolase) inhibitor that inhibits the action of carboxylesterase (EC 3.1.1.1 ).
Alpha-carboxylesterase inhibitor
Alpha-carboxylesterase inhibitors
Beta-esterase inhibitor
Beta-esterase inhibitors
EC 3.1.1.1 (carboxylesterase) inhibitors
ali-esterase inhibitor
ali-esterase inhibitors
butyrate esterase inhibitor
butyrate esterase inhibitors
butyryl esterase inhibitor
butyryl esterase inhibitors
carboxyl ester hydrolase inhibitor
carboxyl ester hydrolase inhibitors
carboxylate esterase inhibitor
carboxylate esterase inhibitors
carboxylesterase inhibitor
carboxylesterase inhibitors
carboxylic acid esterase inhibitor
carboxylic acid esterase inhibitors
carboxylic esterase inhibitor
carboxylic esterase inhibitors
carboxylic-ester hydrolase inhibitor
carboxylic-ester hydrolase inhibitors
cocaine esterase inhibitor
cocaine esterase inhibitors
esterase A inhibitor
esterase A inhibitors
esterase B inhibitor
esterase B inhibitors
esterase D inhibitor
esterase D inhibitors
methylbutyrase inhibitor
methylbutyrase inhibitors
methylbutyrate esterase inhibitor
methylbutyrate esterase inhibitors
monobutyrase inhibitor
monobutyrase inhibitors
nonspecific carboxylesterase inhibitor
nonspecific carboxylesterase inhibitors
procaine esterase inhibitor
procaine esterase inhibitors
propionyl esterase inhibitor
propionyl esterase inhibitors
serine esterase inhibitor
serine esterase inhibitors
triacetin esterase inhibitor
triacetin esterase inhibitors
vitamin A esterase inhibitor
vitamin A esterase inhibitors
EC 3.1.1.1 (carboxylesterase) inhibitor
Alpha-carboxylesterase inhibitor
ChEBI
Alpha-carboxylesterase inhibitors
ChEBI
Beta-esterase inhibitor
ChEBI
Beta-esterase inhibitors
ChEBI
EC 3.1.1.1 (carboxylesterase) inhibitors
ChEBI
ali-esterase inhibitor
ChEBI
ali-esterase inhibitors
ChEBI
butyrate esterase inhibitor
ChEBI
butyrate esterase inhibitors
ChEBI
butyryl esterase inhibitor
ChEBI
butyryl esterase inhibitors
ChEBI
carboxyl ester hydrolase inhibitor
ChEBI
carboxyl ester hydrolase inhibitors
ChEBI
carboxylate esterase inhibitor
ChEBI
carboxylate esterase inhibitors
ChEBI
carboxylesterase inhibitor
ChEBI
carboxylesterase inhibitors
ChEBI
carboxylic acid esterase inhibitor
ChEBI
carboxylic acid esterase inhibitors
ChEBI
carboxylic esterase inhibitor
ChEBI
carboxylic esterase inhibitors
ChEBI
carboxylic-ester hydrolase inhibitor
ChEBI
carboxylic-ester hydrolase inhibitors
ChEBI
cocaine esterase inhibitor
ChEBI
cocaine esterase inhibitors
ChEBI
esterase A inhibitor
ChEBI
esterase A inhibitors
ChEBI
esterase B inhibitor
ChEBI
esterase B inhibitors
ChEBI
esterase D inhibitor
ChEBI
esterase D inhibitors
ChEBI
methylbutyrase inhibitor
ChEBI
methylbutyrase inhibitors
ChEBI
methylbutyrate esterase inhibitor
ChEBI
methylbutyrate esterase inhibitors
ChEBI
monobutyrase inhibitor
ChEBI
monobutyrase inhibitors
ChEBI
nonspecific carboxylesterase inhibitor
ChEBI
nonspecific carboxylesterase inhibitors
ChEBI
procaine esterase inhibitor
ChEBI
procaine esterase inhibitors
ChEBI
propionyl esterase inhibitor
ChEBI
propionyl esterase inhibitors
ChEBI
serine esterase inhibitor
ChEBI
serine esterase inhibitors
ChEBI
triacetin esterase inhibitor
ChEBI
triacetin esterase inhibitors
ChEBI
vitamin A esterase inhibitor
ChEBI
vitamin A esterase inhibitors
ChEBI
Any compound that causes severe skin, eye and mucosal pain and irritation.
blister agent
blister agents
vesicants
vesicant
blister agent
ChEBI
blister agents
ChEBI
vesicants
ChEBI
An amino acid zwitterion obtained by transfer of a proton from the carboxy to the amino group of any alpha-amino acid; major species at pH 7.3.
an alpha-amino acid
alpha-amino acid zwitterion
an alpha-amino acid
UniProt
Any organooxygen compound that is a polyhydroxy-aldehyde or -ketone, or a compound derived from one. Carbohydrates contain only carbon, hydrogen and oxygen and usually have an empirical formula Cm(H2O)n; carbohydrate derivatives may contain other elements by substitution or condensation.
carbohydrates and derivatives
carbohydrates and their derivatives
carbohydrates and carbohydrate derivatives
carbohydrates and derivatives
ChEBI
carbohydrates and their derivatives
ChEBI
Any metabolite produced by all living cells.
essential metabolite
essential metabolites
fundamental metabolites
fundamental metabolite
essential metabolite
ChEBI
essential metabolites
ChEBI
fundamental metabolites
ChEBI
Any organic molecular entity that contains at least one C=C bond.
olefinic compounds
olefinic compound
olefinic compounds
ChEBI
A monocarboxylic acid in which the carbon of the carboxy group is directly attached to a C=C or C#C bond.
2,3-unsaturated monocarboxylic acid
2,3-unsaturated monocarboxylic acids
alpha,beta-unsaturated monocarboxylic acids
alpha,beta-unsaturated monocarboxylic acid
2,3-unsaturated monocarboxylic acid
ChEBI
2,3-unsaturated monocarboxylic acids
ChEBI
alpha,beta-unsaturated monocarboxylic acids
ChEBI
An EC 2.7.11.* (protein-serine/threonine kinase) inhibitor that interferes with the action of mitogen-activated protein kinase (EC 2.7.11.24).
ATP:protein phosphotransferase (MAPKK-activated) inhibitor
ATP:protein phosphotransferase (MAPKK-activated) inhibitors
Dp38 inhibitor
Dp38 inhibitors
EC 2.7.11.24 (mitogen-activated protein kinase) inhibitors
EC 2.7.11.24 inhibitor
EC 2.7.11.24 inhibitors
ERK inhibitor
ERK inhibitors
ERK1 inhibitor
ERK1 inhibitors
ERK2 inhibitor
ERK2 inhibitors
JNK inhibitor
JNK inhibitors
JNK3alpha1 inhibitor
JNK3alpha1 inhibitors
LeMPK3 inhibitor
LeMPK3 inhibitors
MAP kinase inhibitor
MAP kinase inhibitors
MAP-2 kinase inhibitor
MAP-2 kinase inhibitors
MAPK inhibitor
MAPK inhibitors
MBP kinase I inhibitor
MBP kinase I inhibitors
MBP kinase II inhibitor
MBP kinase II inhibitors
MEK inhibitor
MEK inhibitors
PMK-1 inhibitor
PMK-1 inhibitors
PMK-2 inhibitor
PMK-2 inhibitors
PMK-3 inhibitor
PMK-3 inhibitors
SAPK inhibitor
SAPK inhibitors
STK26 inhibitor
STK26 inhibitors
c-Jun N-terminal kinase inhibitor
c-Jun N-terminal kinase inhibitors
extracellular signal-regulated kinase inhibitor
extracellular signal-regulated kinase inhibitors
microtubule-associated protein 2 kinase inhibitor
microtubule-associated protein 2 kinase inhibitors
microtubule-associated protein kinase inhibitor
microtubule-associated protein kinase inhibitors
mitogen-activated protein kinase (EC 2.7.11.24) inhibitor
mitogen-activated protein kinase (EC 2.7.11.24) inhibitors
mitogen-activated protein kinase inhibitor
mitogen-activated protein kinase inhibitors
myelin basic protein kinase inhibitor
myelin basic protein kinase inhibitors
p38-2 inhibitor
p38-2 inhibitors
p38delta inhibitor
p38delta inhibitors
p42 mitogen-activated protein kinase inhibitor
p42 mitogen-activated protein kinase inhibitors
p42(mapk) inhibitor
p42(mapk) inhibitors
p44mpk inhibitor
p44mpk inhibitors
pp42 inhibitor
pp42 inhibitors
pp44(mapk) inhibitor
pp44(mapk) inhibitors
stress-activated protein kinase inhibitor
stress-activated protein kinase inhibitors
EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor
ATP:protein phosphotransferase (MAPKK-activated) inhibitor
ChEBI
ATP:protein phosphotransferase (MAPKK-activated) inhibitors
ChEBI
Dp38 inhibitor
ChEBI
Dp38 inhibitors
ChEBI
EC 2.7.11.24 (mitogen-activated protein kinase) inhibitors
ChEBI
EC 2.7.11.24 inhibitor
ChEBI
EC 2.7.11.24 inhibitors
ChEBI
ERK inhibitor
ChEBI
ERK inhibitors
ChEBI
ERK1 inhibitor
ChEBI
ERK1 inhibitors
ChEBI
ERK2 inhibitor
ChEBI
ERK2 inhibitors
ChEBI
JNK inhibitor
ChEBI
JNK inhibitors
ChEBI
JNK3alpha1 inhibitor
ChEBI
JNK3alpha1 inhibitors
ChEBI
LeMPK3 inhibitor
ChEBI
LeMPK3 inhibitors
ChEBI
MAP kinase inhibitor
ChEBI
MAP kinase inhibitors
ChEBI
MAP-2 kinase inhibitor
ChEBI
MAP-2 kinase inhibitors
ChEBI
MAPK inhibitor
ChEBI
MAPK inhibitors
ChEBI
MBP kinase I inhibitor
ChEBI
MBP kinase I inhibitors
ChEBI
MBP kinase II inhibitor
ChEBI
MBP kinase II inhibitors
ChEBI
MEK inhibitor
ChEBI
MEK inhibitors
ChEBI
PMK-1 inhibitor
ChEBI
PMK-1 inhibitors
ChEBI
PMK-2 inhibitor
ChEBI
PMK-2 inhibitors
ChEBI
PMK-3 inhibitor
ChEBI
PMK-3 inhibitors
ChEBI
SAPK inhibitor
ChEBI
SAPK inhibitors
ChEBI
STK26 inhibitor
ChEBI
STK26 inhibitors
ChEBI
c-Jun N-terminal kinase inhibitor
ChEBI
c-Jun N-terminal kinase inhibitors
ChEBI
extracellular signal-regulated kinase inhibitor
ChEBI
extracellular signal-regulated kinase inhibitors
ChEBI
microtubule-associated protein 2 kinase inhibitor
ChEBI
microtubule-associated protein 2 kinase inhibitors
ChEBI
microtubule-associated protein kinase inhibitor
ChEBI
microtubule-associated protein kinase inhibitors
ChEBI
mitogen-activated protein kinase (EC 2.7.11.24) inhibitor
ChEBI
mitogen-activated protein kinase (EC 2.7.11.24) inhibitors
ChEBI
mitogen-activated protein kinase inhibitor
ChEBI
mitogen-activated protein kinase inhibitors
ChEBI
myelin basic protein kinase inhibitor
ChEBI
myelin basic protein kinase inhibitors
ChEBI
p38-2 inhibitor
ChEBI
p38-2 inhibitors
ChEBI
p38delta inhibitor
ChEBI
p38delta inhibitors
ChEBI
p42 mitogen-activated protein kinase inhibitor
ChEBI
p42 mitogen-activated protein kinase inhibitors
ChEBI
p42(mapk) inhibitor
ChEBI
p42(mapk) inhibitors
ChEBI
p44mpk inhibitor
ChEBI
p44mpk inhibitors
ChEBI
pp42 inhibitor
ChEBI
pp42 inhibitors
ChEBI
pp44(mapk) inhibitor
ChEBI
pp44(mapk) inhibitors
ChEBI
stress-activated protein kinase inhibitor
ChEBI
stress-activated protein kinase inhibitors
ChEBI
Any compound that is added to manufactured materials to inhibit, suppress, or delay the production of flames and so prevent the spread of fire.
flame retardants
flame retardant
flame retardants
ChEBI
Any inorganic anion with a valency of three.
trivalent inorganic anions
trivalent inorganic anion
trivalent inorganic anions
ChEBI
Any inorganic anion with a valency of two.
divalent inorganic anions
divalent inorganic anion
divalent inorganic anions
ChEBI
Any inorganic anion with a valency of one.
monovalent inorganic anions
monovalent inorganic anion
monovalent inorganic anions
ChEBI
Peroxidase
Peroxidase
Peroxidase
KEGG_COMPOUND
A monocarboxylic acid that is the O-phenyl derivative of glycolic acid. A metabolite of 2-phenoxyethanol, it is used in the manufacture of pharmaceuticals, pesticides, fungicides and dyes.
Phenoxyacetic acid
phenoxyacetic acid
Glycol acid phenyl ether
POA
Phenoxyacetate
Phenoxyessigsaeure
phenoxacetic acid
phenoxyethanoic acid
phenoxyacetic acid
Phenoxyacetic acid
KEGG_COMPOUND
phenoxyacetic acid
IUPAC
Glycol acid phenyl ether
HMDB
POA
ChemIDplus
Phenoxyacetate
KEGG_COMPOUND
Phenoxyessigsaeure
ChEBI
phenoxacetic acid
ChEBI
phenoxyethanoic acid
NIST_Chemistry_WebBook
An elemental molecular entity in which all of the atoms have atomic number 26.
elemental iron
Any unsaturated fatty acid anion with one double or triple bond in the fatty acid chain.
monounsaturated fatty acid anions
monounsaturated fatty acid anion
monounsaturated fatty acid anions
ChEBI
A Daphnia metabolite produced by the species Daphnia galeata.
Daphnia galeata metabolites
Daphnia galeata metabolite
Daphnia galeata metabolites
ChEBI
An animal metabolite produced by arthropods such as crabs, lobsters, crayfish, shrimps and krill.
crustacean metabolites
crustacean metabolite
crustacean metabolites
ChEBI
A Daphnia metabolite produced by the species Daphnia magna.
Daphnia magna metabolites
Daphnia magna metabolite
Daphnia magna metabolites
ChEBI
A crustacean metabolite produced by the genus of small planktonic arthropods, Daphnia
Daphnia metabolites
Daphnia metabolite
Daphnia metabolites
ChEBI
Any C-glycosyl compound arising formally from the elimination of water from a glycosidic hydroxy group and an H atom bound to a flavone skeleton, thus creating a C-C bond.
flavone C-glycosides
flavone C-glycoside
flavone C-glycosides
ChEBI
An ester resulting from the formal condensation of the hydroxy group of an alcohol, phenol, heteroarenol, or enol with an organosulfonic acid.
organosulfonate ester
organosulfonate esters
organosulfonic esters
organosulfonic ester
organosulfonate ester
ChEBI
organosulfonate esters
ChEBI
organosulfonic esters
ChEBI
A cyclic tetrapyrrole anion arising from deprotonation of the carboxy group and the C-21 posiiton of chlorophyllide a. It is the major microspecies at pH 7.3 (according to Marvin v 6.2.0.).
chlorophyllide a
chlorophyllide a(2-)
chlorophyllide a
UniProt
A cyclic tetrapyrrole anion that is derived from chlorophyllide b via deprotonation of the carboxy group and formation of a carbide ion. It is the major microspecies at pH 7.3 (according to Marvin v 6.2.0.).
chlorophyllide b
chlorophyllide b(2-)
chlorophyllide b
UniProt
An organosulfate oxoanion obtained by deprotonation of the sulfo group of any alkyl sulfate; major species at pH 7.3.
alkyl sulfate anion
an alkyl sulfate
alkyl sulfate(1-)
alkyl sulfate anion
ChEBI
an alkyl sulfate
UniProt
Any alkane having a chain length of at least 13 carbon atoms.
a long-chain alkane
long-chain alkane
a long-chain alkane
UniProt
Any derivative of a proteinogenic amino acid resulting from reaction at an amino group, carboxy group, or a side-chain functional group, or from the replacement of any hydrogen by a heteroatom.
canonical amino acid derivative
canonical amino acid derivatives
canonical amino-acid derivative
canonical amino-acid derivatives
proteinogenic amino acid derivatives
proteinogenic amino-acid derivative
proteinogenic amino-acid derivatives
proteinogenic amino acid derivative
canonical amino acid derivative
ChEBI
canonical amino acid derivatives
ChEBI
canonical amino-acid derivative
ChEBI
canonical amino-acid derivatives
ChEBI
proteinogenic amino acid derivatives
ChEBI
proteinogenic amino-acid derivative
ChEBI
proteinogenic amino-acid derivatives
ChEBI
Any derivative of a non-proteinogenic amino acid resulting from reaction at an amino group or carboxy group, or from the replacement of any hydrogen by a heteroatom.
non-canonical amino acid derivative
non-canonical amino-acid derivatives
non-proteinogenic amino-acid derivatives
non-proteinogenic amino acid derivative
non-canonical amino acid derivative
ChEBI
non-canonical amino-acid derivatives
ChEBI
non-proteinogenic amino-acid derivatives
ChEBI
Any of the 23 alpha-amino acids that are precursors to proteins, and are incorporated into proteins during translation. The group includes the 20 amino acids encoded by the nuclear genes of eukaryotes together with selenocysteine, pyrrolysine, and N-formylmethionine. Apart from glycine, which is non-chiral, all have L configuration.
canonical amino acid
canonical amino acids
proteinogenic amino acids
proteinogenic amino acid
canonical amino acid
ChEBI
canonical amino acids
ChEBI
proteinogenic amino acids
ChEBI
Any amino-acid that is not naturally encoded in the genetic code of any organism.
non-canonical amino acid
non-canonical amino acids
non-canonical amino-acid
non-canonical amino-acids
non-coded amino acid
non-coded amino acids
non-coded amino-acid
non-coded amino-acids
non-proteinogenic amino acids
non-proteinogenic amino-acid
non-proteinogenic amino-acids
non-proteinogenic amino acid
non-canonical amino acid
ChEBI
non-canonical amino acids
ChEBI
non-canonical amino-acid
ChEBI
non-canonical amino-acids
ChEBI
non-coded amino acid
ChEBI
non-coded amino acids
ChEBI
non-coded amino-acid
ChEBI
non-coded amino-acids
ChEBI
non-proteinogenic amino acids
ChEBI
non-proteinogenic amino-acid
ChEBI
non-proteinogenic amino-acids
ChEBI
Any derivative of an amino acid resulting from reaction at an amino group, carboxy group, side-chain functional group, or from the replacement of any hydrogen by a heteroatom. The definition normally excludes peptides containing amino acid residues.
amino acid derivatives
modified amino acids
amino acid derivative
amino acid derivatives
ChEBI
modified amino acids
ChEBI
Any L-alpha-amino acid which is not a member of the group of 23 proteinogenic amino acids.
non-proteinogenic L-alpha-amino acids
non-proteinogenic L-alpha-amino acid
non-proteinogenic L-alpha-amino acids
ChEBI
Any alpha-amino acid which is not a member of the group of 23 proteinogenic amino acids.
non-proteinogenic alpha-amino acids
non-proteinogenic alpha-amino-acid
non-proteinogenic alpha-amino-acids
non-proteinogenic alpha-amino acid
non-proteinogenic alpha-amino acids
ChEBI
non-proteinogenic alpha-amino-acid
ChEBI
non-proteinogenic alpha-amino-acids
ChEBI
A fatty acid anion obtained by deprotonation of the carboxy group of any 2-saturated fatty acid.
1,2-saturated fatty acid anion
a 1,2-saturated fatty acid
2-saturated fatty acid anion
1,2-saturated fatty acid anion
ChEBI
a 1,2-saturated fatty acid
UniProt
A proteinogenic amino acid derivative resulting from reaction of L-aspartic acid at the amino group or either of the carboxy groups, or from the replacement of any hydrogen of L-aspartic acid by a heteroatom.
L-aspartic acid derivatives
L-aspartic acid derivative
L-aspartic acid derivatives
ChEBI
A proteinogenic amino acid derivative resulting from reaction of L-glutamic acid at the amino group or either of the carboxy groups, or from the replacement of any hydrogen of L-glutamic acid by a heteroatom.
L-glutamic acid derivatives
L-glutamic acid derivative
L-glutamic acid derivatives
ChEBI
Any metabolite (endogenous or exogenous) found in human urine samples.
human urinary metabolites
human urinary metabolite
human urinary metabolites
ChEBI
A non-proteinogenic amino acid derivative resulting from reaction of D-phenylalanine at the amino group or the carboxy group, or from the replacement of any hydrogen of D-phenylalanine by a heteroatom.
D-phenylalanine derivatives
D-phenylalanine derivative
D-phenylalanine derivatives
ChEBI
A proteinogenic amino acid derivative resulting from reaction of L-phenylalanine at the amino group or the carboxy group, or from the replacement of any hydrogen of L-phenylalanine by a heteroatom.
L-phenylalanine derivatives
L-phenylalanine derivative
L-phenylalanine derivatives
ChEBI
Any eukaryotic metabolite produced during a metabolic reaction in algae including unicellular organisms like chlorella and diatoms to multicellular organisms like giant kelps and brown algae.
algal metabolites
algal metabolite
algal metabolites
ChEBI
Any cosmetic used to lighten the colour of skin by reducing the concentration of melanin.
melanogenesis inhibitor
melanogenesis inhibitors
skin bleaching agent
skin bleaching agents
skin depigmenting agent
skin depigmenting agents
skin lightening agents
skin whitening agent
skin whitening agents
skin lightening agent
melanogenesis inhibitor
ChEBI
melanogenesis inhibitors
ChEBI
skin bleaching agent
ChEBI
skin bleaching agents
ChEBI
skin depigmenting agent
ChEBI
skin depigmenting agents
ChEBI
skin lightening agents
ChEBI
skin whitening agent
ChEBI
skin whitening agents
ChEBI
Any metabolite (endogenous or exogenous) found in human blood serum samples.
human blood serum metabolites
human blood serum metabolite
human blood serum metabolites
ChEBI
Any mammalian metabolite produced during a metabolic reaction in rat (Rattus norvegicus).
Rattus norvegicus metabolite
Rattus norvegicus metabolites
rat metabolites
rat metabolite
Rattus norvegicus metabolite
ChEBI
Rattus norvegicus metabolites
ChEBI
rat metabolites
ChEBI
Any antifungal agent used to prevent or treat fungal infections in humans or animals.
anti-fungal drug
anti-fungal drugs
anti-fungal medication
anti-fungal medications
antifungal drugs
antifungal medication
antifungal medications
pharmaceutical fungicide
pharmaceutical fungicides
antifungal drug
anti-fungal drug
ChEBI
anti-fungal drugs
ChEBI
anti-fungal medication
ChEBI
anti-fungal medications
ChEBI
antifungal drugs
ChEBI
antifungal medication
ChEBI
antifungal medications
ChEBI
pharmaceutical fungicide
ChEBI
pharmaceutical fungicides
ChEBI
A metal sulfate in which the metal component is manganese in the +2 oxidation state.
manganese(2+) sulfate
Manganese monosulfate
Manganese sulfate anhydrous
Manganese sulphate
Manganous sulfate
MnSO4
manganese(2+) sulfate
manganese(2+) sulphate
manganese(II) sulphate
manganese(II) sulfate
manganese(2+) sulfate
IUPAC
Manganese monosulfate
ChemIDplus
Manganese sulfate anhydrous
ChemIDplus
Manganese sulphate
ChemIDplus
Manganous sulfate
ChemIDplus
MnSO4
ChEBI
manganese(2+) sulfate
ChEBI
manganese(2+) sulphate
ChEBI
manganese(II) sulphate
ChEBI
Gibberellic acid
A member of the class of acridines that is acridine substituted by a chloro group at position 6, a methoxy group at position 2 and a [5-(diethylamino)pentan-2-yl]nitrilo group at position 9.
4-N-(6-chloro-2-methoxyacridin-9-yl)-1-N,1-N-diethylpentane-1,4-diamine
Quinacrine
2-methoxy-6-chloro-9-diethylaminopentylaminoacridine
3-chloro-7-methoxy-9-(1-methyl-4-diethylaminobutylamino)acridine
6-chloro-9-((4-(diethylamino)-1-methylbutyl)amino)-2-methoxyacridine
Mepacrine
N(4)-(6-chloro-2-methoxy-9-acridinyl)-N(1),N(1)-diethyl-1,4-pentanediamine
mepacrine
quinacrine
4-N-(6-chloro-2-methoxyacridin-9-yl)-1-N,1-N-diethylpentane-1,4-diamine
IUPAC
Quinacrine
KEGG_COMPOUND
2-methoxy-6-chloro-9-diethylaminopentylaminoacridine
ChemIDplus
3-chloro-7-methoxy-9-(1-methyl-4-diethylaminobutylamino)acridine
ChemIDplus
6-chloro-9-((4-(diethylamino)-1-methylbutyl)amino)-2-methoxyacridine
ChemIDplus
Mepacrine
KEGG_COMPOUND
N(4)-(6-chloro-2-methoxy-9-acridinyl)-N(1),N(1)-diethyl-1,4-pentanediamine
ChemIDplus
mepacrine
ChemIDplus
Any metal which causes the onset of an allergic reaction.
allergenic metal
allergenic metals
metal allergens
metal allergen
allergenic metal
ChEBI
allergenic metals
ChEBI
metal allergens
ChEBI
Any drug which causes the onset of an allergic reaction.
allergenic drug
drug allergen
allergenic drug
ChEBI
An EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor that inhibits the action of c-Jun N-terminal kinase.
JNK inhibitor
JNK inhibitors
c-Jun N-terminal kinase inhibitors
c-Jun N-terminal kinase inhibitor
JNK inhibitor
ChEBI
JNK inhibitors
ChEBI
c-Jun N-terminal kinase inhibitors
ChEBI
A drug that acts as an antagonist, agonist, reverse agonist, or in some other fashion when interacting with cellular receptors.
receptor modulators
receptor modulator
receptor modulators
ChEBI
A carboxylic acic anion obtained by deprotonation of the carboxy group of any aromatic carboxylic acid. Major species at pH 7.3.
an aromatic carboxylate
aromatic carboxylate
an aromatic carboxylate
UniProt