CHEBI:15772 - L-dopachrome

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ChEBI Name L-dopachrome
ChEBI ID CHEBI:15772
ChEBI ASCII Name L-dopachrome
Definition The L-enantiomer of dopachrome.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:13099, CHEBI:21281, CHEBI:6212
Supplier Information
Download Molfile XML SDF
Formula C9H7NO4
Net Charge 0
Average Mass 193.15622
Monoisotopic Mass 193.038
InChI InChI=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
InChIKey VJNCICVKUHKIIV-LURJTMIESA-N
SMILES [H][C@]1(CC2=CC(=O)C(=O)C=C2N1)C(O)=O
Metabolite of Species Details
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Roles Classification
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 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 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 Sources
2-L-Carboxy-2,3-dihydroindole-5,6-quinone KEGG COMPOUND
L-Dopachrome KEGG COMPOUND
Manual Xref Database
C01693 KEGG COMPOUND
View more database links
Registry Number Type Source
5532979 Beilstein Registry Number Beilstein
Last Modified
27 January 2016