Fasudil

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Chemical Structure| 103745-39-7 同义名 : AT877;HA-1077
CAS号 : 103745-39-7
货号 : A702414
分子式 : C14H17N3O2S
纯度 : 96%
分子量 : 291.369
MDL号 : MFCD00866182
存储条件:

Pure form Keep in dark place,Sealed in dry,Store in freezer, under -20°C

In solvent -20°C:3-6个月-80°C:12个月

溶解度 : -
动物实验配方:
生物活性
描述 Fasudil hydrochloride is a potent inhibitor of ROCK-II, PKA, PKG, PKC, and MLCK with Ki of 0.33 μM, 1.6 μM, 1.6 μM, 3.3 μM and 36 μM, respectively.
临床研究
NCT号 适应症或疾病 临床期 招募状态 预计完成时间 地点
NCT01069042 Heart Failure Phase 4 Unknown November 2010 Taiwan ... 展开 >> National Cheng Kung University Hospital Recruiting Tainan, Taiwan, 70401 Contact: Ping-Yen Liu, MD, PhD 收起 <<
NCT03404843 Cardiovascular Diseases Phase 2 Completed - United States, Colorado ... 展开 >> Colorado State University, Dept. of Health and Exercise Science Fort Collins, Colorado, United States, 80523 收起 <<
NCT01823081 Diabetic Macular Edema Phase 3 Completed - Iran, Islamic Republic of ... 展开 >> Tehran, Iran, Islamic Republic of 收起 <<
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

3.43mL

0.69mL

0.34mL

17.16mL

3.43mL

1.72mL

34.32mL

6.86mL

3.43mL

参考文献

[1]Zhang J, Li XX, et al. Inhibition of the activity of Rho-kinase reduces cardiomyocyte apoptosis in heart ischemia/reperfusion via suppressing JNK-mediated AIF translocation. Clin Chim Acta. 2009 Mar;401(1-2):76-80.

[2]Ono-Saito N, Niki I, et al. H-series protein kinase inhibitors and potential clinical applications. Pharmacol Ther. 1999 May-Jun;82(2-3):123-31.