生物活性 | |||
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描述 | FT709 is a potent and selective inhibitor of USP9X, with an IC50 of 82 nM. USP9X is associated with centrosome function, chromosome alignment during mitosis, EGFR degradation, chemo-sensitization, and regulation of circadian rhythms[1]. |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.01mL 0.40mL 0.20mL |
10.03mL 2.01mL 1.00mL |
20.06mL 4.01mL 2.01mL |
参考文献 |
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