| CAS： | 867017-68-3 |
| 分子式： | C18H13ClF2N6O |
| 分子量： | 402.79 |
| 纯度： | ≥98% |
| 溶解性： | DMSO |
| 存储： | Powder -20℃ 3 years; 4℃ 2 years In solvent -80℃ 6 months;-20℃ 1 month |
| 研究领域： | Cardiovascular Disease |
| Target： | IC50: 0.6 nM (Human ROCK-1), 1.1 nM (Human ROCK-2), 2.4 nM (Murine ROCK-2), 0.8 nM (Rat ROCK-2)[1] |
| 描述： | Azaindole 1 is a highly potent inhibitor of human ROCK-1 and ROCK-2, with IC50 of 0.6 and 1.1 nM, respectively, and also inhibits murine ROCK-2 or rat ROCK-2 with IC50 of 2.4 and 0.8 nM, respectively. |
