CHEBI:70006 - 3ʼ,5-dihydroxy-3,4ʼ,5ʼ,7-tetramethoxyflavone

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ChEBI Name 3ʼ,5-dihydroxy-3,4ʼ,5ʼ,7-tetramethoxyflavone
ChEBI ID CHEBI:70006
ChEBI ASCII Name 3',5-dihydroxy-3,4',5',7-tetramethoxyflavone
Definition A tetramethoxyflavone that is myricetin in which the hydroxy groups at positions 3, 7, 4ʼ and 5ʼ have been replaced by methoxy groups. It has been isolated from Combretum quadrangulare.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C19H18O8
Net Charge 0
Average Mass 374.34140
Monoisotopic Mass 374.10017
InChI InChI=1S/C19H18O8/c1-23-10-7-11(20)15-13(8-10)27-17(19(26-4)16(15)22)9-5-12(21)18(25-3)14(6-9)24-2/h5-8,20-21H,1-4H3
InChIKey LLDTYMGZAXZDDU-UHFFFAOYSA-N
SMILES COc1cc(O)c2c(c1)oc(-c1cc(O)c(OC)c(OC)c1)c(OC)c2=O
Metabolite of Species Details
Combretum quadrangulare (IPNI:170410-1) Found in leaf (BTO:0000713). Methanolic extract of leaves 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.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 3ʼ,5-dihydroxy-3,4ʼ,5ʼ,7-tetramethoxyflavone (CHEBI:70006) has functional parent myricetin (CHEBI:18152)
3ʼ,5-dihydroxy-3,4ʼ,5ʼ,7-tetramethoxyflavone (CHEBI:70006) has role metabolite (CHEBI:25212)
3ʼ,5-dihydroxy-3,4ʼ,5ʼ,7-tetramethoxyflavone (CHEBI:70006) has role plant metabolite (CHEBI:76924)
3ʼ,5-dihydroxy-3,4ʼ,5ʼ,7-tetramethoxyflavone (CHEBI:70006) is a dihydroxyflavone (CHEBI:38686)
3ʼ,5-dihydroxy-3,4ʼ,5ʼ,7-tetramethoxyflavone (CHEBI:70006) is a tetramethoxyflavone (CHEBI:76875)
IUPAC Name
5-hydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-3,7-dimethoxy-4H-chromen-4-one
Synonyms Sources
5-hydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-3,7-dimethoxy-4H-1-benzopyran-4-one ChemIDplus
myricetin 3,7,3ʼ,4ʼ-tetramethyl ether ChEBI
Manual Xref Database
LMPK12112792 LIPID MAPS
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Registry Numbers Types Sources
1406939 Reaxys Registry Number Reaxys
14290-57-4 CAS Registry Number ChemIDplus
Citation Waiting for Citations Type Source
21265555 PubMed citation Europe PMC
Last Modified
06 January 2014