InChI=1S/C9H7NO4/c11-7-2-4-1-6(9(13)14)10-5(4)3-8(7)12/h1-3,10-12H,(H,13,14) |
YFTGOBNOJKXZJC-UHFFFAOYSA-N |
OC(=O)C1=CC2=CC(O)=C(O)C=C2N1 |
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Mus musculus
(NCBI:txid10090)
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Source: BioModels - MODEL1507180067
See:
PubMed
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mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
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View more via ChEBI Ontology
Outgoing
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5,6-dihydroxyindole-2-carboxylic acid
(CHEBI:2003)
has role
mouse metabolite
(CHEBI:75771)
5,6-dihydroxyindole-2-carboxylic acid
(CHEBI:2003)
is a
dihydroxyindole
(CHEBI:23781)
5,6-dihydroxyindole-2-carboxylic acid
(CHEBI:2003)
is conjugate acid of
5,6-dihydroxyindole-2-carboxylate
(CHEBI:16875)
5,6-dihydroxyindole-2-carboxylic acid
(CHEBI:2003)
is tautomer of
dopachrome
(CHEBI:49108)
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Incoming
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indole-5,6-quinone-2-carboxylic acid
(CHEBI:81394)
has functional parent
5,6-dihydroxyindole-2-carboxylic acid
(CHEBI:2003)
5,6-dihydroxyindole-2-carboxylate
(CHEBI:16875)
is conjugate base of
5,6-dihydroxyindole-2-carboxylic acid
(CHEBI:2003)
dopachrome
(CHEBI:49108)
is tautomer of
5,6-dihydroxyindole-2-carboxylic acid
(CHEBI:2003)
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5,6-dihydroxy-1H-indole-2-carboxylic acid
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5,6-DHICA
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ChemIDplus
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5,6-dihydroxy-2-indolecarboxylic acid
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ChemIDplus
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5,6-dihydroxy-2-indolylcarboxylic acid
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ChemIDplus
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5,6-Dihydroxyindole-2-carboxylate
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KEGG COMPOUND
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DHI2C
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ChemIDplus
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DHICA
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KEGG COMPOUND
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168167
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Reaxys Registry Number
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Reaxys
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4790-08-3
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CAS Registry Number
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ChemIDplus
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