CHEBI:3162 - bowdichione

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ChEBI Name bowdichione
ChEBI ID CHEBI:3162
Definition A hydroxyisoflavone with a quinone structure in ring B. Isolated from Dalbergia parviflora, it exhibits antineoplastic and anti-inflammatory activities.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C16H10O6
Net Charge 0
Average Mass 298.24700
Monoisotopic Mass 298.04774
InChI InChI=1S/C16H10O6/c1-21-15-6-12(18)10(5-13(15)19)11-7-22-14-4-8(17)2-3-9(14)16(11)20/h2-7,17H,1H3
InChIKey GCAIEHBYLQNGAF-UHFFFAOYSA-N
SMILES COC1=CC(=O)C(=CC1=O)c1coc2cc(O)ccc2c1=O
Roles Classification
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
anti-inflammatory agent
Any compound that has anti-inflammatory effects.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing bowdichione (CHEBI:3162) has role anti-inflammatory agent (CHEBI:67079)
bowdichione (CHEBI:3162) has role antineoplastic agent (CHEBI:35610)
bowdichione (CHEBI:3162) has role metabolite (CHEBI:25212)
bowdichione (CHEBI:3162) is a 1,4-benzoquinones (CHEBI:132124)
bowdichione (CHEBI:3162) is a hydroxyisoflavone (CHEBI:38755)
bowdichione (CHEBI:3162) is a methoxyisoflavone (CHEBI:38756)
bowdichione (CHEBI:3162) is a oxoisoflavone (CHEBI:50278)
IUPAC Name
2-(7-hydroxy-4-oxo-4H-chromen-3-yl)-5-methoxybenzo-1,4-quinone
Synonym Source
Bowdichione KEGG COMPOUND
Manual Xrefs Databases
C00002511 KNApSAcK
C10202 KEGG COMPOUND
View more database links
Registry Numbers Types Sources
1656717 Beilstein Registry Number Beilstein
1656717 Reaxys Registry Number Reaxys
53774-75-7 CAS Registry Number KEGG COMPOUND
Citations Waiting for Citations Types Sources
19928832 PubMed citation Europe PMC
9525107 PubMed citation Europe PMC
Last Modified
03 June 2016