CHEBI:112106 - (R)-3-(indol-3-yl)-2-oxobutyric acid

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name (R)-3-(indol-3-yl)-2-oxobutyric acid ChEBI ID CHEBI:112106 ChEBI ASCII Name (R)-3-(indol-3-yl)-2-oxobutyric acid Definition The (R)-enantiomer of 3-(indol-3-yl)-2-oxobutyric acid. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C12H11NO3 Net Charge 0 Average Mass 217.221 Monoisotopic Mass 217.07389 InChI InChI=1S/C12H11NO3/c1-7(11(14)12(15)16)9-6-13-10-5-3-2-4-8(9)10/h2-7,13H,1H3,(H,15,16)/t7-/m1/s1 InChIKey VSANSNPZLCXLRK-SSDOTTSWSA-N SMILES C12=CC=CC=C1C(=CN2)[C@@H](C)C(C(O)=O)=O Metabolite of Species Details Streptomyces griseus (NCBI:txid1911) of strain ATCC 12648 See: PubMed Roles Classification Chemical Role(s): Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Bronsted base). (via oxoacid ) Biological Role(s): bacterial metabolite Any prokaryotic metabolite produced during a metabolic reaction in bacteria. View more via ChEBI Ontology ChEBI Ontology Outgoing (R)-3-(indol-3-yl)-2-oxobutyric acid (CHEBI:112106) has role bacterial metabolite (CHEBI:76969) (R)-3-(indol-3-yl)-2-oxobutyric acid (CHEBI:112106) is a 3-(indol-3-yl)-2-oxobutyric acid (CHEBI:28549) (R)-3-(indol-3-yl)-2-oxobutyric acid (CHEBI:112106) is conjugate acid of (R)-3-(indol-3-yl)-2-oxobutyrate (CHEBI:91180) (R)-3-(indol-3-yl)-2-oxobutyric acid (CHEBI:112106) is enantiomer of (S)-3-(indol-3-yl)-2-oxobutyric acid (CHEBI:16083) Incoming (R)-3-(indol-3-yl)-2-oxobutyrate (CHEBI:91180) is conjugate base of (R)-3-(indol-3-yl)-2-oxobutyric acid (CHEBI:112106) (S)-3-(indol-3-yl)-2-oxobutyric acid (CHEBI:16083) is enantiomer of (R)-3-(indol-3-yl)-2-oxobutyric acid (CHEBI:112106) IUPAC Name (3R)-3-(1H-indol-3-yl)-2-oxobutanoic acid Synonym Source (R)-β-methylindolepyruvic acid ChEBI Manual Xref Database CPD-398 MetaCyc View more database links Registry Number Type Source 26479367 Reaxys Registry Number Reaxys Citation Type Source 25730866 PubMed citation Europe PMC Last Modified 11 April 2016