CHEBI:31064 - 2'-hydroxybiochanin A

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ChEBI Name 2'-hydroxybiochanin A
ChEBI ID CHEBI:31064
Definition A methoxyisoflavone in which the methoxy group is located at position 4' together with three additional hydroxy substituents at positions 2' 5 and 7.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C16H12O6
Net Charge 0
Average Mass 300.26290
Monoisotopic Mass 300.06339
InChI InChI=1S/C16H12O6/c1-21-9-2-3-10(12(18)6-9)11-7-22-14-5-8(17)4-13(19)15(14)16(11)20/h2-7,17-19H,1H3
InChIKey OZEVXMDBOINMTC-UHFFFAOYSA-N
SMILES COc1ccc(c(O)c1)-c1coc2cc(O)cc(O)c2c1=O
Metabolite of Species Details
Pycnanthus angolensis (NCBI:txid224864) See: PubMed
Roles Classification
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
apoptosis inducer
Any substance that induces the process of apoptosis (programmed cell death) in multi-celled organisms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2'-hydroxybiochanin A (CHEBI:31064) has role apoptosis inducer (CHEBI:68495)
2'-hydroxybiochanin A (CHEBI:31064) has role plant metabolite (CHEBI:76924)
2'-hydroxybiochanin A (CHEBI:31064) is a 2'-hydroxyisoflavones (CHEBI:28206)
2'-hydroxybiochanin A (CHEBI:31064) is a 4'-methoxyisoflavones (CHEBI:133959)
2'-hydroxybiochanin A (CHEBI:31064) is a 7-hydroxyisoflavones (CHEBI:55465)
2'-hydroxybiochanin A (CHEBI:31064) is a methoxyisoflavone (CHEBI:38756)
IUPAC Name
5,7-dihydroxy-3-(2-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one
Synonyms Sources
2'-Hydroxybiochanin A KEGG COMPOUND
5,7,2'-Trihydroxy-4'-methoxyisoflavone KNApSAcK
Dehydroferreirin KEGG COMPOUND
Manual Xrefs Databases
C00009457 KNApSAcK
C12135 KEGG COMPOUND
LMPK12050328 LIPID MAPS
View more database links
Registry Numbers Types Sources
1325822 Reaxys Registry Number Reaxys
32884-35-8 CAS Registry Number KNApSAcK
Citation Waiting for Citations Type Source
21495101 PubMed citation Europe PMC
Last Modified
16 June 2015