CHEBI:37025 - D-2-aminoadipic acid

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ChEBI Name D-2-aminoadipic acid
ChEBI ID CHEBI:37025
ChEBI ASCII Name D-2-aminoadipic acid
Definition An optically active form of 2-aminoadipic acid having D-configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C6H11NO4
Net Charge 0
Average Mass 161.15588
Monoisotopic Mass 161.06881
InChI InChI=1S/C6H11NO4/c7-4(6(10)11)2-1-3-5(8)9/h4H,1-3,7H2,(H,8,9)(H,10,11)/t4-/m1/s1
InChIKey OYIFNHCXNCRBQI-SCSAIBSYSA-N
SMILES N[C@H](CCCC(O)=O)C(O)=O
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
mammalian metabolite
Any animal metabolite produced during a metabolic reaction in mammals.
(via 2-aminoadipic acid )
Caenorhabditis elegans metabolite
A nematode metabolite produced by Caenorhabditis elegans.
(via 2-aminoadipic acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing D-2-aminoadipic acid (CHEBI:37025) has role metabolite (CHEBI:25212)
D-2-aminoadipic acid (CHEBI:37025) is a 2-aminoadipic acid (CHEBI:37024)
D-2-aminoadipic acid (CHEBI:37025) is enantiomer of L-2-aminoadipic acid (CHEBI:37023)
Incoming L-2-aminoadipic acid (CHEBI:37023) is enantiomer of D-2-aminoadipic acid (CHEBI:37025)
IUPAC Name
(2R)-2-aminohexanedioic acid
Synonym Source
D-α-aminoadipic acid ChEBI
Registry Numbers Types Sources
1724347 Reaxys Registry Number Reaxys
1724347 Beilstein Registry Number Beilstein
7620-28-2 CAS Registry Number ChemIDplus
Citation Waiting for Citations Type Source
22770225 PubMed citation Europe PMC
Last Modified
05 November 2012