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USP8-IN-2 是一种有效的去泛素化酶 USP7和USP8 抑制剂,对USP8D 的IC50为4.0 μM。USP8-IN-2是治疗癌症和病毒感染的潜在化合物。
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USP8-IN-2 是一种有效的去泛素化酶 USP7和USP8 抑制剂,对USP8D 的IC50为4.0 μM。USP8-IN-2是治疗癌症和病毒感染的潜在化合物。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 635 | In stock | |
5 mg | ¥ 1,560 | In stock | |
10 mg | ¥ 2,430 | In stock | |
25 mg | ¥ 3,950 | In stock | |
50 mg | ¥ 5,690 | In stock | |
100 mg | ¥ 7,680 | In stock | |
500 mg | ¥ 15,300 | In stock | |
1 mL x 10 mM (in DMSO) | ¥ 1,780 | In stock |
USP8-IN-2 相关产品
产品描述 | USP8-IN-2 is a potent inhibitor of the deubiquitinating enzymes USP7 and USP8, with an IC50 of 4.0 μM against USP8D. USP8-IN-2 is a potential compound for the treatment of cancer and viral infections. |
靶点活性 | USP8:6.0 μM |
体外活性 | USP8-IN-3通过抑制H1957细胞的增殖,展现出抑制活性,其GI50值为24.93 μM[1]。 |
分子量 | 444.9 |
分子式 | C19H20ClF3N4OS |
CAS No. | 2477651-11-7 |
Smiles | C(F)(F)(F)C1=NC(=CC=C1)N2CCC(NC(NC3=C(OC)C=CC(Cl)=C3)=S)CC2 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 27.5 mg/mL (61.81 mM), Sonication is recommended. ![]() | ||||||||||||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||||||||||||
DMSO
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以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
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