CHEBI:86262 - D-kynurenine

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ChEBI Name D-kynurenine
ChEBI ASCII Name D-kynurenine
Definition A kynurenine that has D configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C10H12N2O3
Net Charge 0
Average Mass 208.21390
Monoisotopic Mass 208.08479
InChI InChI=1S/C10H12N2O3/c11-7-4-2-1-3-6(7)9(13)5-8(12)10(14)15/h1-4,8H,5,11-12H2,(H,14,15)/t8-/m1/s1
SMILES N[C@H](CC(=O)c1ccccc1N)C(O)=O
Metabolite of Species Details
Rattus norvegicus (NCBI:txid10116) See: PubMed
Homo sapiens (NCBI:txid9606) See: PubMed
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): human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via kynurenine )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing D-kynurenine (CHEBI:86262) has role human metabolite (CHEBI:77746)
D-kynurenine (CHEBI:86262) is a D-α-amino acid (CHEBI:16733)
D-kynurenine (CHEBI:86262) is a kynurenine (CHEBI:28683)
D-kynurenine (CHEBI:86262) is enantiomer of L-kynurenine (CHEBI:16946)
Incoming L-kynurenine (CHEBI:16946) is enantiomer of D-kynurenine (CHEBI:86262)
(2R)-2-amino-4-(2-aminophenyl)-4-oxobutanoic acid
Registry Numbers Types Sources
13441-51-5 CAS Registry Number ChemIDplus
3206278 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
24158577 PubMed citation Europe PMC
25030849 PubMed citation Europe PMC
26041992 PubMed citation Europe PMC
Last Modified
01 July 2015