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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.
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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 |
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. |
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