7,3',4'-trihydroxy-3,8-dimethoxyflavone (CHEBI:69452)

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ChEBI Name	7,3',4'-trihydroxy-3,8-dimethoxyflavone

ChEBI ID	CHEBI:69452

Definition	A trihydroxyflavone that is flavone substituted by hydroxy groups at positions 7, 3' and 4' and methoxy groups at positions 3 and 8. Isolated from Mimosa diplotricha, it exhibits cytotoxic activity against human cancer cell lines.

Stars	This entity has been manually annotated by the ChEBI Team.

Supplier Information	We are unable to retrieve the vendor information for this entry at this time. Please try again later.

Download	Molfile XML SDF

Formula

C17H14O7

Net Charge

Average Mass

330.28890

Monoisotopic Mass

330.07395

InChI

InChI=1S/C17H14O7/c1-22-16-11(19)6-4-9-13(21)17(23-2)14(24-15(9)16)8-3-5-10(18)12(20)7-8/h3-7,18-20H,1-2H3

InChIKey

LLXQONIKJLTKCF-UHFFFAOYSA-N

SMILES

COc1c(O)ccc2c1oc(-c1ccc(O)c(O)c1)c(OC)c2=O

Metabolite of Species	Details
Mimosa diplotricha (NCBI:txid512270)	Found in aerial part (BTO:0001658). Ethanolic extract of aerial part 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):	antineoplastic agent A substance that inhibits or prevents the proliferation of neoplasms.

ChEBI Ontology
Outgoing	7,3',4'-trihydroxy-3,8-dimethoxyflavone (CHEBI:69452) has functional parent flavone (CHEBI:42491) 7,3',4'-trihydroxy-3,8-dimethoxyflavone (CHEBI:69452) has role antineoplastic agent (CHEBI:35610) 7,3',4'-trihydroxy-3,8-dimethoxyflavone (CHEBI:69452) has role metabolite (CHEBI:25212) 7,3',4'-trihydroxy-3,8-dimethoxyflavone (CHEBI:69452) is a catechols (CHEBI:33566) 7,3',4'-trihydroxy-3,8-dimethoxyflavone (CHEBI:69452) is a dimethoxyflavone (CHEBI:23798) 7,3',4'-trihydroxy-3,8-dimethoxyflavone (CHEBI:69452) is a trihydroxyflavone (CHEBI:27116)

IUPAC Name

2-(3,4-dihydroxyphenyl)-7-hydroxy-3,8-dimethoxy-4H-chromen-4-one

Registry Number	Type	Source
1329302	Reaxys Registry Number	Reaxys

Citation

Last Modified

20 March 2018