CHEBI:60872 - leucodopachrome

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ChEBI Name leucodopachrome
ChEBI ID CHEBI:60872
Definition Indoline substituted with hydroxy groups at C-5 and -6 and a carboxy group at C-2, and with S stereochemistry at C-2.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter R. Stephan
Supplier Information
Download Molfile XML SDF
Formula C9H9NO4
Net Charge 0
Average Mass 195.17210
Monoisotopic Mass 195.053
InChI InChI=1S/C9H9NO4/c11-7-2-4-1-6(9(13)14)10-5(4)3-8(7)12/h2-3,6,10-12H,1H2,(H,13,14)/t6-/m0/s1
InChIKey JDWYRSDDJVCWPB-LURJTMIESA-N
SMILES OC(=O)[C@@H]1Cc2cc(O)c(O)cc2N1
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): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing leucodopachrome (CHEBI:60872) has role metabolite (CHEBI:25212)
leucodopachrome (CHEBI:60872) is a hydroxy monocarboxylic acid (CHEBI:35868)
leucodopachrome (CHEBI:60872) is a indoles (CHEBI:24828)
Incoming cyclodopa 5-β-D-glucoside (CHEBI:134458) has functional parent leucodopachrome (CHEBI:60872)
IUPAC Name
(2S)-5,6-dihydroxy-2,3-dihydro-1H-indole-2-carboxylic acid
Synonyms Sources
(S)-2-carboxy-5,6-dihydroxyindoline ChEBI
(S)-5,6-dihydroxyindoline-2-carboxylic acid ChEBI
cyclo-Dopa KEGG COMPOUND
cyclodopa SUBMITTER
L-2-carboxy-2,3-dihydro-5,6-dihydroxyindole SUBMITTER
Leucodopachrome KEGG COMPOUND
Leukodopachrome ChemIDplus
Manual Xref Database
C05604 KEGG COMPOUND
View more database links
Registry Numbers Types Sources
18766-67-1 CAS Registry Number KEGG COMPOUND
18766-67-1 CAS Registry Number ChemIDplus
480086 Beilstein Registry Number Beilstein
Citation Waiting for Citations Type Source
11987411 PubMed citation SUBMITTER
Last Modified
30 June 2017
General Comment
2011-01-04 Intermediate in melanin biosynthesis.