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CHEBI:15772 - L-dopachrome

ChEBI IDCHEBI:15772
ChEBI NameL-dopachrome
Stars
ASCII NameL-dopachrome
DefinitionThe L-enantiomer of dopachrome.
Secondary ChEBI IDsCHEBI:6212, CHEBI:13099, CHEBI:21281
Last Modified27 January 2016
DownloadsMolfile
FormulaC9H7NO4
Net Charge0
Average Mass193.158
Monoisotopic Mass193.03751
SMILES[H][C@@]1(C(=O)O)CC2=CC(=O)C(=O)C=C2N1
InChIInChI=1S/C9H7NO4/c11-7-2-4-1-6(9(13)14)10-5(4)3-8(7)12/h2-3,6,10H,1H2,(H,13,14)/t6-/m0/s1
InChIKeyVJNCICVKUHKIIV-LURJTMIESA-N
Species of MetaboliteComponentSourceComments
Mus musculus (ncbitaxon:10090) - PubMed (19425150) Source: BioModels - MODEL1507180067
Roles Classification
Biological Role:
mouse metabolite  Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
ChEBI Ontology
Outgoing Relation(s)
L-dopachrome (CHEBI:15772) has role mouse metabolite (CHEBI:75771)
L-dopachrome (CHEBI:15772) is a dopachrome (CHEBI:49108)
L-dopachrome (CHEBI:15772) is conjugate acid of L-dopachromate (CHEBI:57509)
L-dopachrome (CHEBI:15772) is enantiomer of D-dopachrome (CHEBI:49109)
Incoming Relation(s)
L-dopachromate (CHEBI:57509) is conjugate base of L-dopachrome (CHEBI:15772)
D-dopachrome (CHEBI:49109) is enantiomer of L-dopachrome (CHEBI:15772)
IUPAC Name 
(2S)-5,6-dioxo-2,3,5,6-tetrahydro-1H-indole-2-carboxylic acid
Synonyms  Source
2-L-Carboxy-2,3-dihydroindole-5,6-quinoneKEGG COMPOUND
L-DopachromeKEGG COMPOUND
Manual XrefsDatabases
C01693KEGG COMPOUND
Registry NumbersSources
Beilstein:5532979Beilstein