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Ginkgetin

Drug details:
Molecular formula: C32H22O10

Classification: Biflavonoids and polyflavonoids; Flavonoids; Phenylpropanoids and polyketides; Organic compounds;
Synonyms:  7,4'-Dimethylamentoflavone
Amentoflavone 7,4'-dimethyl ether
5,7-dihydroxy-8-[5-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)-2-methoxyphenyl]-2-(4-hydroxyphenyl)chromen-4-one
4H-1-Benzopyran-4-one, 5,7-dihydroxy-8-(5-(5-hydroxy-7-methoxy-4-oxo-4H-1-benzopyran-2-yl)-2-methoxyphenyl)-2-(4-hydroxyphenyl)-
4H-1-Benzopyran-4-one, 5,7-dihydroxy-8-[5-(5-hydroxy-7-methoxy-4-oxo-4H-1-benzopyran-2-yl)-2-methoxyphenyl]-2-(4-hydroxyphenyl)-
5,7-dihydroxy-8-[5-(5-hydroxy-7-methoxy-4-oxo-4H-1-benzopyran-2-yl)-2-methoxyphenyl]-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
5,7-dihydroxy-8-(5-(5-hydroxy-7-methoxy-4-oxo-4H-1-benzopyran-2-yl)-2-methoxyphenyl)-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
Ginkgetin 7''-O-beta-D-glucopyranoside
5,7-dihydroxy-8-[5-(5-hydroxy-7-methoxy-4-oxo-chromen-2-yl)-2-methoxy-phenyl]-2-(4-hydroxyphenyl)chromen-4-one
......

Chemical structure:
Depiction based on curated SMILES HO O OH O O OH O O CH 3 O CH 3 OH

Evidence for compound's anti-virulence activity:

Streptococcus
Related VF: Suilysin
Target: Sly
Drug effect: Suppresses the process of oligomerization to inhibit Suilysin activity.
Max phase: Preclinical (in vivo)
Publication:
Li G, et al., 2019. Ginkgetin in vitro and in vivo reduces Streptococcus suis virulence by inhibiting suilysin activity. J Appl Microbiol 127(5):1556-1563.








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