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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:28804 -
D
-2-aminopentanoic acid
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ChEBI Name
D
-2-aminopentanoic acid
ChEBI ID
CHEBI:28804
ChEBI ASCII Name
D-2-aminopentanoic acid
Definition
A 2-aminopentanoic acid that has
R
-configuration.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:4217, CHEBI:20890
Supplier Information
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Formula
C5H11NO2
Net Charge
0
Average Mass
117.14638
Monoisotopic Mass
117.07898
InChI
InChI=1S/C5H11NO2/c1-2-3-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)/t4-/m1/s1
InChIKey
SNDPXSYFESPGGJ-SCSAIBSYSA-N
SMILES
CCC[C@@H](N)C(O)=O
Roles Classification
Chemical Role
(s):
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Br
o
nsted acid).
(via
organic amino compound
)
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
Biological Role
(s):
EC 6.1.1.4 (leucine--tRNA ligase) inhibitor
An EC 6.1.1.* (ligases forming aminoacyl tRNA and related compounds) inhibitor that inhibits the action of leucine
tRNA synthetase (EC 6.1.1.4).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
D
-2-aminopentanoic acid (
CHEBI:28804
)
has role
EC 6.1.1.4 (leucine—tRNA ligase) inhibitor (
CHEBI:77953
)
D
-2-aminopentanoic acid (
CHEBI:28804
)
is a
2-aminopentanoic acid (
CHEBI:19475
)
D
-2-aminopentanoic acid (
CHEBI:28804
)
is a
D
-α-amino acid (
CHEBI:16733
)
D
-2-aminopentanoic acid (
CHEBI:28804
)
is enantiomer of
L
-2-aminopentanoic acid (
CHEBI:18314
)
Incoming
L
-2-aminopentanoic acid (
CHEBI:18314
)
is enantiomer of
D
-2-aminopentanoic acid (
CHEBI:28804
)
IUPAC Name
(2
R
)-2-aminopentanoic acid
Synonyms
Sources
(
R
)-norvaline
ChEBI
D-2-Aminopentanoic acid
KEGG COMPOUND
D-2-Aminovaleric acid
KEGG COMPOUND
D
-Ape
JCBN
D-Norvaline
Note: (2004-12-13) IUPAC recommends progressive abandonment of 'nor' in the naming of amino acids (see 3AA-15.2.3).
KEGG COMPOUND
D
-Nva
ChEBI
Manual Xrefs
Databases
C01799
KEGG COMPOUND
CN101007774
Patent
View more database links
Registry Numbers
Types
Sources
1721161
Reaxys Registry Number
Reaxys
2013-12-9
CAS Registry Number
KEGG COMPOUND
2013-12-9
CAS Registry Number
ChemIDplus
Citations
Types
Sources
31071709
PubMed citation
Europe PMC
35625327
PubMed citation
Europe PMC
Last Modified
25 August 2022