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HA 1077, Dihydrochloride-CAS 103745-39-7-Calbiochem
产品编号: | 4061687 |
规格: | A cell-permeable, reversible, and ATP-competitive Ca2+ antagonist with anti-vasospastic properties. |
CAS NO: | 103745-39-7 |
包装规格: | 1 MG |
产品类别: | 进口试剂 |
品牌: | Sigma-Aldrich |
优惠价: | 立即咨询 |
产品价格查看更多规格...
产品编号 | 包装单位 | 单价(元) | 国内现货 | 国外库存 | 询价单 |
4061687 | 1 MG | 2150 |
产品别名
103745-39-7
HA 1077, Dihydrochloride-CAS 103745-39-7-Calbiochem
Fasudil, (5-Isoquinolinesulfonyl)homopiperazine, 2HCl, PKG Inhibitor VII
基本信息
Empirical Formula【经验(实验)分子式】 | C14H17N3O2S · 2HCl |
Molecular weight | 364.29 |
General description【一般描述】 | A cell-permeable, reversible, and ATP-competitive Ca2+ antagonist with anti-vasospastic properties. Inhibits protein kinase A (Ki = 1.6 µM), protein kinase G (Ki = 1.6 µM), and myosin light chain kinase (Ki = 3.6 µM). Also reported to potently inhibit Rho-associated kinase (ROCK; IC50 = 10.7 µM). Prevents apoptosis and enhances the survival and cloning efficiency of dissociated hES cells without affecting their pluripotency. A cell-permeable, reversible, and ATP-competitive Ca2+ antagonist with anti-vasospastic properties. Inhibits protein kinase A (Ki = 1.6 µM), protein kinase G (Ki = 1.6 µM), and myosin light chain kinase (Ki = 36 µM). Also reported to potently inhibit Rho-associated kinase (ROCK; IC50 = 10.7 µM). Prevents apoptosis and enhances the survival and cloning efficiency of dissociated hES cells without affecting their pluripotency. |
Biochem/physiol Actions【生化/生理作用】 | Cell permeable: yes Target IC50: 10.7 µM inhibiting Rho-associated kinase (ROCK) Product competes with ATP. Target Ki: .6 µM, 1.6 µM, 36 µM, inhibiting protein kinase A, protein kinase G, myosin light chain kinase, respectively Reversible: yes Primary Target PKA |
Warning【警告】 | Toxicity: Harmful (C) |
Reconstitution【重悬】 | Following reconstitution, refrigerate (4°C). Aqueous stock solutions are stable for up to 6 months at 4°C. |
Other Notes【其他说明】 | Watanabe, K., et al. 2007. Nature Biotech.25, 681. Swärd, K., et al. 2000. J. Physiol.522, 33. Takizawa, S., et al. 1993. Eur. J. Pharmacol. 250, 431. Seto, M., et al. 1991. Eur. J. Pharmacol.195, 267. Shirotani, M., et al. 1991. J. Pharmacol. Exp. Ther.259, 738. Asano, T., et al. 1990. Eur. J. Pharmacol.190, 365. Sasaki, Y., and Sasaki, Y. 1990. Biochem. Biophys. Res. Commun.171, 1182. Asano, T., et al. 1989. Br. J. Pharmacol. 98,1091. |
Legal Information【法律信息】 | CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany |
产品性质
Quality Level【质量水平】 | 100 |
Assay【测定】 | ≥98% (HPLC) |
form【形式】 | solid |
manufacturer/tradename | Calbiochem® |
storage condition【储存条件】 | OK to freeze |
color【颜色】 | white |
solubility【溶解性】 | water: 1 mg/mL |
shipped in【运输】 | ambient |
storage temp.【储存温度】 | 2-8℃ |
InChI | 1S/C14H17N3O2S/c18-20(19,17-9-2-6-15-8-10-17)14-4-1-3-12-11-16-7-5-13(12)14/h1,3-5,7,11,15H,2,6,8-10H2 |
InChI key | NGOGFTYYXHNFQH-UHFFFAOYSA-N |
packaging【包装】 | 1 mg in Plastic ampoule |
安全信息
Storage Class Code【储存分类代码】 | 11 - Combustible Solids |
WGK | WGK 3 |