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Merck
CN

208665

氯化卡咪唑

A cell-permeable calmodulin antagonist.

别名:

氯化卡咪唑, 化合物R 24571

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关于此项目

经验公式(希尔记法):
C31H23Cl7N2O
化学文摘社编号:
分子量:
687.70
UNSPSC Code:
12352200
MDL number:
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产品名称

氯化卡咪唑, A cell-permeable calmodulin antagonist.

InChI

1S/C31H24Cl6N2O.Cl/c32-23-6-1-20(2-7-23)31(21-3-8-24(33)9-4-21)39-14-13-38(19-39)17-30(27-12-11-26(35)16-29(27)37)40-18-22-5-10-25(34)15-28(22)36;/h1-16,30-31H,17-19H2;

InChI key

LBFGPQFQXRJXDI-UHFFFAOYSA-N

assay

≥95% (HPLC)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze

color

white

solubility

DMSO: 10 mg/mL
ethanol: 10 mg/mL

shipped in

ambient

storage temp.

−20°C

Quality Level

Biochem/physiol Actions

主要靶标
脑钙调蛋白依赖性磷酸二酯酶
产物不与ATP竞争。
可逆:否
细胞可渗透性:是
靶标IC50:10 nM,针对脑钙调蛋白依赖性磷酸二酯酶

Disclaimer

在水溶液中容易粘附在玻璃上。
毒性:标准处理(A)

General description

注意:在水溶液中容易粘附在玻璃上。
细胞可渗透的钙调蛋白拮抗剂。sepazonium的类似物作为脑Ca2+-钙调蛋白依赖性磷酸二酯酶(IC50=10 nM)的抑制剂,其效力至少是三氟拉嗪(目录编号642150)的150倍。抑制电压门控Ca2+通道并刺激神经母细胞瘤细胞释放一氧化氮。还充当红细胞中钙依赖性Ca2+-ATPase的强抑制剂。已知可延长体内心脏不应期。
细胞可渗透的钙调蛋白拮抗剂。作为脑钙调蛋白依赖性磷酸二酯酶(IC50=10 nM)的抑制剂,其效力至少是三氟拉嗪(目录编号642150)的150倍。电压门控Ca2+通道的抑制剂。刺激神经母细胞瘤细胞释放一氧化氮。还充当骨骼肌肌浆网Ca2+-ATPase(Ki=60 nM)的强非竞争性抑制剂。已知可延长体内心脏不应期。

Other Notes

Hu, J., and El-Fakahany, E.E.1993.NeuroReport.4, 198.
Nakazawa, K., et al. 1993.Br. J. Pharmacol.109, 137.
Yuasa, T., and Muto, S. 1992.Arch.Biochem.Biophys.296, 175.
Ichikawa, M., et al. 1991.J. Membrane Biol.120, 211.
Silver, P.J., et al. 1989.Cardiovasc.Drug Ther.3, 675.
Anderson, K.W., et al. 1984.J. Biol. Chem.259, 11487.
Gietzen, L., et al. 1982.Biochem.J. 207, 541.
Van Belle, H. 1981.Cell Calcium2, 483.
Levin, R.N., and Weiss, B. 1979.J. Pharmacol.Exp.Therap.208, 454.

Preparation Note

复溶后,等分并冷冻长期保存(-20°C),或冷藏(4°C)短期保存。DMSO储备溶液在-20°C下可稳定保存2个月。

Legal Information

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

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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