InChI=1S/C16H12O7/c1- 22- 16- 14(21) 13- 11(20) 5- 8(17) 6- 12(13) 23- 15(16) 7- 2- 3- 9(18) 10(19) 4- 7/h2- 6,17- 20H,1H3 |
WEPBGSIAWZTEJR-UHFFFAOYSA-N |
COc1c(oc2cc(O)cc(O)c2c1=O)-c1ccc(O)c(O)c1 |
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Ficus mucuso
(NCBI:txid309328)
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Found in
fruit
(BTO:0000486).
Methanolic extract of air-dried and powdered figs(fruits)
See:
PubMed
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Ophioglossum pedunculosum
(NCBI:txid60874)
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Found in
whole plant
(BTO:0001461).
75% EtOH extract of dried whole plant
See:
PubMed
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metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
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View more via ChEBI Ontology
Outgoing
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3',4',5,7-tetrahydroxy-3-methoxyflavone
(CHEBI:16860)
has functional parent
quercetin
(CHEBI:16243)
3',4',5,7-tetrahydroxy-3-methoxyflavone
(CHEBI:16860)
has role
antimicrobial agent
(CHEBI:33281)
3',4',5,7-tetrahydroxy-3-methoxyflavone
(CHEBI:16860)
has role
metabolite
(CHEBI:25212)
3',4',5,7-tetrahydroxy-3-methoxyflavone
(CHEBI:16860)
is a
monomethoxyflavone
(CHEBI:25401)
3',4',5,7-tetrahydroxy-3-methoxyflavone
(CHEBI:16860)
is a
tetrahydroxyflavone
(CHEBI:38684)
3',4',5,7-tetrahydroxy-3-methoxyflavone
(CHEBI:16860)
is conjugate acid of
3',4',5-trihydroxy-3-methoxyflavon-7-olate
(CHEBI:57928)
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Incoming
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3-O-methylquercetin 7-O-β-glucopyranosyl-4ʼ-O-β-D-glucopyranoside
(CHEBI:67938)
has functional parent
3',4',5,7-tetrahydroxy-3-methoxyflavone
(CHEBI:16860)
3',4',5-trihydroxy-3-methoxyflavon-7-olate
(CHEBI:57928)
is conjugate base of
3',4',5,7-tetrahydroxy-3-methoxyflavone
(CHEBI:16860)
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2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-methoxy-4H-chromen-4-one
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2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-methoxy-4H-1-benzopyran-4-one
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ChemIDplus
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3',4',5,7-Tetrahydroxy-3-methoxyflavone
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KEGG COMPOUND
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3-methoxy-5,7,3',4'-tetrahydroxyflavone
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ChEBI
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3-Methoxy-5,7,3',4'-tetrahydroxyflavone
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KEGG COMPOUND
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3-O-Methylquercetin
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KEGG COMPOUND
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1486-70-0
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CAS Registry Number
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ChemIDplus
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324509
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Reaxys Registry Number
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Reaxys
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16213685
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PubMed citation
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Europe PMC
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22418930
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PubMed citation
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Europe PMC
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23207251
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PubMed citation
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Europe PMC
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9396391
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PubMed citation
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Europe PMC
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