CHEBI:16514 - 4',5,7-trihydroxy-3'-methoxyflavone

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 4',5,7-trihydroxy-3'-methoxyflavone
ChEBI ID CHEBI:16514
Definition The 3'-O-methyl derivative of luteolin.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:12083, CHEBI:2006, CHEBI:20519
Supplier Information
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Roles Classification
Chemical Role(s): antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
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.
Related Structures
4',5,7-trihydroxy-3'-methoxyflavone is a Functional Parent of
7-O-(6-p-coumaroylglucosyl)chrysoeriol
Mass : 608.54620
Formula : C31H28O13
75509
7-O-[alpha-L-rhamnosyl-(1->2)-beta-D-glucosyl]chrysoeriol
Mass : 608.54470
Formula : C28H32O15
75523
geraldone
Mass : 284.26350
Formula : C16H12O5
5326
6-C-(alpha-L-arabinosyl)-8-C-(beta-L-arabinosyl)chrysoeriol
Mass : 564.493
Formula : C26H28O14
131758
chrysoeriol 7-O-gentiobioside
Mass : 624.54410
Formula : C28H32O16
75398
velutin
Mass : 314.293
Formula : C17H14O6
177047
isoscoparin
Mass : 462.40348
Formula : C22H22O11
18200
4',5,7-trihydroxy-3'-methoxyflavone is a Structural Derivative of
luteolin
Mass : 286.239
Formula : C15H10O6
15864 		1-benzopyran phenylpropanoid
Definition : Any organic aromatic compound with a structure based on a phenylpropane skeleton. The class includes naturally occurring phenylpropanoid esters, flavonoids, anthocyanins, coumarins and many small phenolic molecules as well as their semi-synthetic and synthetic analogues. Phenylpropanoids are also precursors of lignin.
4',5,7-trihydroxy-3'-methoxyflavone is a Conjugate Acid of
4',5-dihydroxy-3'-methoxyflavon-7-olate(1-)
Mass : 299.25490
Formula : C16H11O6
57799
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