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CHEBI:65780 - 7,4'-dihydroxy-3'-methoxyisoflavone

ChEBI IDCHEBI:65780
ChEBI Name7,4'-dihydroxy-3'-methoxyisoflavone
Stars
DefinitionA member of the class of 7-hydroxyisoflavones that is 7,4'-dihydroxyisoflavone substituted by a methoxy group at position 3'. It is isolated from the heart woods of Maackia amurensis subsp buergeri and Dalbergia louveli and exhibits antiplasmodial ativity.
Last Modified9 October 2024
DownloadsMolfile
FormulaC16H12O5
Net Charge0
Average Mass284.267
Monoisotopic Mass284.06847
SMILESCOc1cc(-c2coc3cc(O)ccc3c2=O)ccc1O
InChIInChI=1S/C16H12O5/c1-20-15-6-9(2-5-13(15)18)12-8-21-14-7-10(17)3-4-11(14)16(12)19/h2-8,17-18H,1H3
InChIKeyMUYAUELJBWQNDH-UHFFFAOYSA-N
Species of MetaboliteComponentSourceComments
Dalbergia louveli (IPNI:490305-1) heartwood (PO:0004512) PubMed (14640516)
Maackia amurensissubsp.buergeri (IPNI:885548-1) heartwood (PO:0004512) DOI (10.1248/cpb.20.2488)
Roles Classification
Biological Roles:
metabolite  Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
antiplasmodial drug  An antiparasitic drug which is effective against Apicomplexan parasites in the genus Plasmodium. The genus contains over 200 species and includes those responsible for malaria.
Application:
antiplasmodial drug  An antiparasitic drug which is effective against Apicomplexan parasites in the genus Plasmodium. The genus contains over 200 species and includes those responsible for malaria.
ChEBI Ontology
Outgoing Relation(s)
7,4'-dihydroxy-3'-methoxyisoflavone (CHEBI:65780) has role antiplasmodial drug (CHEBI:64915)
7,4'-dihydroxy-3'-methoxyisoflavone (CHEBI:65780) has role metabolite (CHEBI:25212)
7,4'-dihydroxy-3'-methoxyisoflavone (CHEBI:65780) is a 7-hydroxyisoflavones (CHEBI:55465)
7,4'-dihydroxy-3'-methoxyisoflavone (CHEBI:65780) is a methoxyisoflavone (CHEBI:38756)
IUPAC Name 
7-hydroxy-3-(4-hydroxy-3-methoxyphenyl)-4H-chromen-4-one
Synonym  Source
3'-methoxydaidzeinChemIDplus
Manual XrefsDatabases
4477721ChemSpider
Registry NumbersSources
Reaxys:1257927Reaxys
CAS:21913-98-4ChemIDplus
Citations