CHEBI:66493 - yinyanghuo B

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ChEBI Name yinyanghuo B
ChEBI ID CHEBI:66493
Definition A trihydroxyflavone that is flavone substituted by hydroxy groups at positions 5, 7 and 4', a 2-hydroxy-3-methylbut-3-en-1-yl group at position 3' and a prenyl group at position 5'. Isolated from Epimedium sagittatum, it exhibits inhibitory activity against platelet aggregation.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C25H26O6
Net Charge 0
Average Mass 422.47030
Monoisotopic Mass 422.17294
InChI InChI=1S/C25H26O6/c1-13(2)5-6-15-7-16(8-17(25(15)30)9-19(27)14(3)4)22-12-21(29)24-20(28)10-18(26)11-23(24)31-22/h5,7-8,10-12,19,26-28,30H,3,6,9H2,1-2,4H3
InChIKey FIZBURLMLRCZTA-UHFFFAOYSA-N
SMILES CC(C)=CCc1cc(cc(CC(O)C(C)=C)c1O)-c1cc(=O)c2c(O)cc(O)cc2o1
Metabolite of Species Details
Epimedium sagittatum (NCBI:txid253616) Found in leaf (BTO:0000713). See: PubMed
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): platelet aggregation inhibitor
A drug or agent which antagonizes or impairs any mechanism leading to blood platelet aggregation, whether during the phases of activation and shape change or following the dense-granule release reaction and stimulation of the prostaglandin-thromboxane system.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing yinyanghuo B (CHEBI:66493) has role metabolite (CHEBI:25212)
yinyanghuo B (CHEBI:66493) has role platelet aggregation inhibitor (CHEBI:50427)
yinyanghuo B (CHEBI:66493) is a secondary alcohol (CHEBI:35681)
yinyanghuo B (CHEBI:66493) is a trihydroxyflavone (CHEBI:27116)
IUPAC Name
5,7-dihydroxy-2-[4-hydroxy-3-(2-hydroxy-3-methylbut-3-en-1-yl)-5-(3-methylbut-2-en-1-yl)phenyl]-4H-chromen-4-one
Manual Xref Database
LMPK12110417 LIPID MAPS
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Citation Waiting for Citations Type Source
8699184 PubMed citation Europe PMC
Last Modified
15 July 2013