CHEBI:133721 - rhamnacene

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ChEBI Name rhamnacene
ChEBI ID CHEBI:133721
Definition A dimethoxyflavone that is quercetin in which the hydroxy groups at the 3' and 7 positions have been replaced by methoxy groups.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C17H14O7
Net Charge 0
Average Mass 330.292
Monoisotopic Mass 330.07395
InChI InChI=1S/C17H14O7/c1-22-9-6-11(19)14-13(7-9)24-17(16(21)15(14)20)8-3-4-10(18)12(5-8)23-2/h3-7,18-19,21H,1-2H3
InChIKey MYMGKIQXYXSRIJ-UHFFFAOYSA-N
SMILES COC1=CC(O)=C2C(=O)C(O)=C(OC2=C1)C1=CC(OC)=C(O)C=C1
Metabolite of Species Details
Rhamnus petiolaris (IPNI: 718561-1) See: Phytochemistry, 1974, 13(5), 857-860.
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): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
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ChEBI Ontology
Outgoing rhamnacene (CHEBI:133721) has functional parent quercetin (CHEBI:16243)
rhamnacene (CHEBI:133721) has role antineoplastic agent (CHEBI:35610)
rhamnacene (CHEBI:133721) has role plant metabolite (CHEBI:76924)
rhamnacene (CHEBI:133721) is a aromatic ether (CHEBI:35618)
rhamnacene (CHEBI:133721) is a dimethoxyflavone (CHEBI:23798)
rhamnacene (CHEBI:133721) is a phenols (CHEBI:33853)
rhamnacene (CHEBI:133721) is a trihydroxyflavone (CHEBI:27116)
rhamnacene (CHEBI:133721) is conjugate acid of rhamnacene-3-olate (CHEBI:192768)
Incoming viscumneoside IV (CHEBI:132858) has functional parent rhamnacene (CHEBI:133721)
viscumneoside VII (CHEBI:132861) has functional parent rhamnacene (CHEBI:133721)
rhamnacene-3-olate (CHEBI:192768) is conjugate base of rhamnacene (CHEBI:133721)
IUPAC Name
3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-4H-chromen-4-one
Synonyms Sources
3',7-dimethylquercetin ChemIDplus
3,5,4'-trihydroxy-7,3'-dimethoxyflavone ChEBI
rhamnazin ChEBI
Manual Xref Database
Rhamnazin Wikipedia
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Registry Numbers Types Sources
338203 Reaxys Registry Number Reaxys
552-54-5 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
11594002 PubMed citation Europe PMC
25704088 PubMed citation Europe PMC
27025066 PubMed citation Europe PMC
35723317 PubMed citation Europe PMC
Last Modified
05 August 2022