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同义名 : | - |
CAS号 : | 2413991-74-7 | |
货号 : | A1600990 | |
分子式 : | C23H22N4O7S | |
纯度 : | 98% | |
分子量 : | 498.51 | |
MDL号 : | N/A | |
存储条件: |
Pure form Sealed in dry, 2-8°C In solvent -20°C:3-6个月-80°C:12个月 |
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溶解度 : | - | |
动物实验配方: |
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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