您的购物车当前为空
HSD1590 is a highly effective and potent inhibitor of ROCK1 and ROCK2, with IC50 values of 1.22 nM and 0.51 nM, respectively. It demonstrates exceptional binding affinity to ROCK, with Kd values below 2 nM. Moreover, HSD1590 showcases minimal cytotoxicity, making it an ideal compound for various applications.


为众多的药物研发团队赋能,
让新药发现更简单!
HSD1590 is a highly effective and potent inhibitor of ROCK1 and ROCK2, with IC50 values of 1.22 nM and 0.51 nM, respectively. It demonstrates exceptional binding affinity to ROCK, with Kd values below 2 nM. Moreover, HSD1590 showcases minimal cytotoxicity, making it an ideal compound for various applications.
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 2 mg | ¥ 3,190 | 5日内发货 | |
| 5 mg | ¥ 3,730 | 5日内发货 | |
| 25 mg | ¥ 13,300 | 6-8周 | |
| 50 mg | ¥ 17,400 | 6-8周 | |
| 100 mg | ¥ 26,600 | 6-8周 | |
| 1 mL x 10 mM (in DMSO) | ¥ 4,120 | 5日内发货 |
| 产品描述 | HSD1590 is a highly effective and potent inhibitor of ROCK1 and ROCK2, with IC50 values of 1.22 nM and 0.51 nM, respectively. It demonstrates exceptional binding affinity to ROCK, with Kd values below 2 nM. Moreover, HSD1590 showcases minimal cytotoxicity, making it an ideal compound for various applications. |
| 靶点活性 | ROCK1:1.22 nM (IC50), ROCK2:0.51 nM (IC50) |
| 体外活性 | HSD1590 (0.5-1 μM; 24 hours) exhibits an impressive attenuation in migration[1]. HSD1590 (0.5-10 μM; 12-24 horus) shows that the excellent migration inhibition observed is not due to cell death, but inhibition of live cell migration[1]. Cell Viability Assay[1]Cell Line: MDA-MB-23 cells Concentration: 0.5-10 μM Incubation Time: 12-24 hours Result: Exhibited approximately 80% viability at 12 hours and yielded an overall viability of 63% at 24 h. |
| 分子量 | 359.19 |
| 分子式 | C20H18BN3O3 |
| CAS No. | 2379279-96-4 |
| Smiles | COc1c(cccc1-c1nc2ccc3[nH]ncc3c2c2CCCc12)B(O)O |
| 密度 | 1.43 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. |
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