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CHEBI:67493 - ombuin

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ChEBI Name ombuin
Definition A dimethoxyflavone that is quercetin in which the hydroxy groups at positions 7 and 4ʼ are replaced by methoxy groups. Isolated from Cyperus teneriffae, it exhibits anti-inflammatory activity.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C17H14O7
Net Charge 0
Average Mass 330.28890
Monoisotopic Mass 330.074
InChI InChI=1S/C17H14O7/c1-22-9-6-11(19)14-13(7-9)24-17(16(21)15(14)20)8-3-4-12(23-2)10(18)5-8/h3-7,18-19,21H,1-2H3
SMILES COc1cc(O)c2c(c1)oc(-c1ccc(OC)c(O)c1)c(O)c2=O
Metabolite of Species Details
Cyperus teneriffae (IPNI:306106-1) Found in root (BTO:0001188). Ethanolic extract of dried roots 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.
Application(s): anti-inflammatory agent
Any compound that has anti-inflammatory effects.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing ombuin (CHEBI:67493) has functional parent quercetin (CHEBI:16243)
ombuin (CHEBI:67493) has role anti-inflammatory agent (CHEBI:67079)
ombuin (CHEBI:67493) has role plant metabolite (CHEBI:76924)
ombuin (CHEBI:67493) is a dimethoxyflavone (CHEBI:23798)
ombuin (CHEBI:67493) is a flavonols (CHEBI:28802)
ombuin (CHEBI:67493) is a trihydroxyflavone (CHEBI:27116)
Synonyms Sources
3,5-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-methoxy-4H-1-benzopyran-4-one ChemIDplus
4ʼ,7-dimethoxy-3,3ʼ,5-trihydroxyflavone ChemIDplus
7,4ʼ-di-O-methylquercetin ChEBI
Database Links Databases
Ombuin Wikipedia
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Registry Numbers Types Sources
338215 Reaxys Registry Number Reaxys
529-40-8 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
18384188 PubMed citation Europe PMC
21504148 PubMed citation Europe PMC
22673832 PubMed citation Europe PMC
23186307 PubMed citation Europe PMC
377475 Chinese Abstracts citation Europe PMC
9690352 PubMed citation Europe PMC
IND20626918 Agricola citation Europe PMC
Last Modified
09 January 2014