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Merck
CN
所有图片(1)

主要文件

681629

Sigma-Aldrich

W-7盐酸盐

A cell-permeable and reversible calmodulin antagonist that inhibits myosin light chain kinase (IC₅₀ = 51 µM) and Ca2+-calmodulin-dependent phosphodiesterase (IC₅₀ = 28 µM).

别名:

W-7盐酸盐, N-(6-氨基己基)-5-氯-1-萘磺酰胺盐酸盐

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About This Item

经验公式(希尔记法):
C16H21ClN2O2S · xHCl
CAS号:
分子量:
340.87 (free base basis)
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.77

质量水平

方案

≥98% (TLC)

表单

crystalline solid

制造商/商品名称

Calbiochem®

储存条件

OK to freeze
desiccated (hygroscopic)
protect from light

颜色

off-white

溶解性

DMSO: 5 mg/mL
DMF: soluble
warm ethanol: soluble

运输

ambient

储存温度

2-8°C

SMILES字符串

[S](=O)(=O)(NCCCCCCN)c1c2c(c(ccc2)Cl)ccc1.[Cl-].[H+]

InChI

1S/C16H21ClN2O2S.ClH/c17-15-9-5-8-14-13(15)7-6-10-16(14)22(20,21)19-12-4-2-1-3-11-18;/h5-10,19H,1-4,11-12,18H2;1H

InChI key

OMMOSRLIFSCDBL-UHFFFAOYSA-N

一般描述

一种细胞渗透性和可逆性钙调蛋白拮抗剂,可抑制肌球蛋白轻链激酶(IC50 = 51 µM)和Ca2+-钙调蛋白依赖性磷酸二酯酶(IC50 = 28 µM)。
一种细胞渗透性和可逆性钙调蛋白拮抗剂,抑制Ca2+-钙调蛋白依赖性磷酸二酯酶(C50 = 28 µM)和肌球蛋白轻链激酶(IC50 = 51 µMM)。

生化/生理作用

主靶
肌球蛋白轻链激酶
产物不与ATP竞争。
可逆性:是
细胞可渗透性:是
靶标IC50:51µM,抑制肌球蛋白轻链激酶;28µM,抑制Ca2+-钙调蛋白依赖性磷酸二酯酶

警告

毒性:标准处理(A)

其他说明

Caulfield, M.P., et al. 1991.Neurosci. Lett.125, 57.
Asano, M. 1989.J. Pharmacol.Exp.Ther.251, 764.
Itoh, H., and Hidaka, H. 1984.J. Biochem.96, 1721.
Tanaka, T., et al. 1983.Pharmacol.26, 249.
Hidaka, H. 1981.Proc.Natl.Acad.Sci. USA 78, 4354.

法律信息

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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