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MI-1061 is a orally bioavailable inhibitor of MDM2 (MDM2-p53 interaction) (IC50=4.4 nM).
MI-1061 is a orally bioavailable inhibitor of MDM2 (MDM2-p53 interaction) (IC50=4.4 nM).
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
2 mg | 待询 | 5日内发货 | |
25 mg | ¥ 27,700 | 6-8周 | |
50 mg | 待询 | 6-8周 | |
100 mg | 待询 | 6-8周 |
MI-1061 相关产品
产品描述 | MI-1061 is a orally bioavailable inhibitor of MDM2 (MDM2-p53 interaction) (IC50=4.4 nM). |
靶点活性 | MDM2:4.4 nM , MDM2:(ki)0.16 nM |
体外活性 | MI-1061 achieves IC50 of 100 and 250 nM in the SJSA-1 and HCT-116 p53+/+ cell lines, respectively[1]. |
体内活性 | MI-1061 was able to achieve tumor regression in oral SJSA-1 xenograft model mice[1]. |
分子量 | 582.45 |
分子式 | C30H26Cl2FN3O4 |
CAS No. | 1410737-34-6 |
密度 | 1.51 g/cm3 (Predicted) |
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: 300 mg/mL (515.07 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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