Powder: -20°C for 3 years
In solvent: -80°C for 2 years
5,7-DIMETHOXYFLAVONE possessed remarkable leishmanicidal potential.
Description | 5,7-DIMETHOXYFLAVONE possessed remarkable leishmanicidal potential. |
In vitro | The best in vitro trypanocidal activity for T. brucei rhodesiense was exerted by 7,8-dihydroxyflavone (50% inhibitory concentration [IC50], 68 ng/ml), followed by 3-hydroxyflavone, rhamnetin, and 7,8,3',4'-tetrahydroxyflavone (IC50s, 0.5 microg/ml) and catechol (IC50, 0.8 microg/ml).?The activity against T. cruzi was moderate, and only Chrysin dimethylether and 3-hydroxydaidzein had IC50s less than 5.0 microg/ml. |
Molecular Weight | 282.295 |
Formula | C17H14O4 |
CAS No. | 21392-57-4 |
Powder: -20°C for 3 years
In solvent: -80°C for 2 years
DMSO: 10 mM
( < 1 mg/ml refers to the product slightly soluble or insoluble )
You can also refer to dose conversion for different animals. More
bottom
Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc.
5,7-DIMETHOXYFLAVONE 21392-57-4 代谢 微生物学 Anti-infection P450 anti-inflammatory Cytochrome P450 Anti-obesity CYPs 5,7 DIMETHOXYFLAVONE inhibit CYP3As antineoplastic BCRP 5,7-Dimethoxyflavone Inhibitor 5,7DIMETHOXYFLAVONE inhibitor