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ChEBI
> Main
CHEBI:32114 - salicylamide
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ChEBI Name
salicylamide
ChEBI ID
CHEBI:32114
Definition
The simplest member of the class of salicylamides derived from salicylic acid.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C7H7NO2
Net Charge
0
Average Mass
137.13600
Monoisotopic Mass
137.04768
InChI
InChI=1S/C7H7NO2/c8-7(10)5-3-1-2-4-6(5)9/h1-4,9H,(H2,8,10)
InChIKey
SKZKKFZAGNVIMN-UHFFFAOYSA-N
SMILES
NC(=O)c1ccccc1O
Roles Classification
Biological Role
(s):
non-narcotic analgesic
A drug that has principally analgesic, antipyretic and anti-inflammatory actions. Non-narcotic analgesics do not bind to opioid receptors.
Application
(s):
non-narcotic analgesic
A drug that has principally analgesic, antipyretic and anti-inflammatory actions. Non-narcotic analgesics do not bind to opioid receptors.
antirheumatic drug
A drug used to treat rheumatoid arthritis.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
salicylamide (
CHEBI:32114
)
has role
antirheumatic drug (
CHEBI:35842
)
salicylamide (
CHEBI:32114
)
has role
non-narcotic analgesic (
CHEBI:35481
)
salicylamide (
CHEBI:32114
)
is a
phenols (
CHEBI:33853
)
salicylamide (
CHEBI:32114
)
is a
salicylamides (
CHEBI:53443
)
Incoming
acetic acid [2-[[(5-nitro-2-thiazolyl)amino]-oxomethyl]phenyl] ester (
CHEBI:94807
)
has functional parent
salicylamide (
CHEBI:32114
)
acetic acid [2-[[(6,6-dimethoxy-3-oxo-1-cyclohexa-1,4-dienyl)amino]-oxomethyl]phenyl] ester (
CHEBI:93534
)
has functional parent
salicylamide (
CHEBI:32114
)
exalamide (
CHEBI:31585
)
has functional parent
salicylamide (
CHEBI:32114
)
salicylanilides (
CHEBI:53468
)
is a
salicylamide (
CHEBI:32114
)
IUPAC Name
2-hydroxybenzamide
INNs
Sources
salicilamida
ChemIDplus
salicylamide
KEGG DRUG
salicylamidum
ChemIDplus
Synonyms
Sources
2-Carbamoylphenol
ChemIDplus
2-Carboxamidophenol
ChemIDplus
2-Hydroxybenzamide
ChemIDplus
o-Hydroxybenzamide
ChemIDplus
OHB
NIST Chemistry WebBook
Salicylic Acid amide
NIST Chemistry WebBook
Manual Xrefs
Databases
2415
DrugCentral
D01811
KEGG DRUG
DB08797
DrugBank
OHB
PDBeChem
Salicylamide
Wikipedia
View more database links
Registry Numbers
Types
Sources
142521
Gmelin Registry Number
Gmelin
65-45-2
CAS Registry Number
ChemIDplus
65-45-2
CAS Registry Number
NIST Chemistry WebBook
742439
Beilstein Registry Number
Beilstein
742439
Reaxys Registry Number
Reaxys
Citations
Types
Sources
14729655
PubMed citation
Europe PMC
1650428
PubMed citation
Europe PMC
22530891
PubMed citation
Europe PMC
Last Modified
22 February 2017