leucodopachrome (CHEBI:60872)

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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

Average Mass

195.17210

Monoisotopic Mass

195.05316

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.

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

Citation	Type	Source
11987411	PubMed citation	SUBMITTER

Last Modified

30 June 2017

General Comment
2011-01-04	Intermediate in melanin biosynthesis.