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USP1-IN-4(compound 10)是一种IC50为2.44 nM的USP1抑制剂,具备抗癌活性,并且与多种抗癌药物表现出协同效应。

USP1-IN-4(compound 10)是一种IC50为2.44 nM的USP1抑制剂,具备抗癌活性,并且与多种抗癌药物表现出协同效应。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 10 mg | 待询 | 10-14周 | |
| 50 mg | 待询 | 10-14周 |
| 产品描述 | USP1-IN-4 (compound 10) serves as a potent inhibitor of USP1, exhibiting an IC 50 of 2.44 nM. It demonstrates anticancer properties and operates synergistically with various anticancer drugs [1]. |
| 靶点活性 | USP1:2.44 nM |
| 体外活性 | USP1-IN-4, at concentrations ranging from 0.0005 to 10 μM, significantly inhibits USP1/UAF1 activity with an IC50 of 2.44 nM following a 15-minute treatment [1]. Additionally, USP1-IN-4 impedes the growth of MDA-MB-436 cells over a 7-day period, also within the 0.0005 to 10 μM range, yielding an IC50 of 103.75 nM [1]. In a cell viability assay using the MDA-MB-436 cell line, a concentration range of 0.0005 to 10 μM was used, and cell growth inhibition was observed with an IC50 of 103.75 nM. |
| 分子量 | 476.50 |
| 分子式 | C26H23F3N6 |
| CAS No. | 2878441-72-4 |
| Smiles | C(C=1N2C(C=NC(=N2)C3=C(C(C)C)C=CC=C3)=CN1)C4=CC=C(C=C4)C5=NC(C(F)(F)F)=CN5C |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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。
对于不同动物的给药剂量换算,您也可以参考 更多