CHEBI:2631 - amentoflavone

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name amentoflavone
ChEBI ID CHEBI:2631
Definition A biflavonoid that is obtained by oxidative coupling of two molecules of apigenin resulting in a bond between positions C-3 of the hydroxyphenyl ring and C-8 of the chromene ring. A natural product found particularly in Ginkgo biloba and Hypericum perforatum.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:65403
Supplier Information
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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.
P450 inhibitor
An enzyme inhibitor that interferes with the activity of cytochrome P450 involved in catalysis of organic substances.
cathepsin B inhibitor
A cysteine protease inhibitor which inhibits cathepsin B (EC 3.4.22.1).
antiviral agent
A substance that destroys or inhibits replication of viruses.
Application(s): angiogenesis inhibitor
An agent and endogenous substances that antagonize or inhibit the development of new blood vessels.
Related Structures
amentoflavone is a Functional Parent of
sciadopitysin
Mass : 580.53770
Formula : C33H24O10
9050 		2,3-dihydro-4',4'''-di-O-methylamentoflavone
Mass : 568.52700
Formula : C32H24O10
65770 		ginkgetin
Mass : 566.51110
Formula : C32H22O10
5353
amentoflavone is a Structural Derivative of
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.
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