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Hesperadin-CAS 422513-13-1-Calbiochem

品牌
Sigma-Aldrich
CAS
422513-13-1
货号
375680
规格纯度
Hesperadin primarily used in Inhibition.
价格
2764.15 *本价格含增值税费
促销
服务
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数量
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半岛bd体育手机客户端 名称:
422513-13-1
Hesperadin-CAS 422513-13-1-Calbiochem
Mammalian Ste20-like Kinase 4 Inhibitor, MST4 Inhibitor, Aurora Kinase Inhibitor X, AMPK Inhibitor II
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半岛bd体育手机客户端 说明

一般描述

A cell-permeable indolinone compound that interacts with both the ATP- and the adjacent hydrophobic binding pocket of Aurora B and acts as a rapid and reversible inhibitor of Aurora kinase B activity (IC50~ 250 nM) with moderate selectivity over Cdk1/B, Cdk2/E and Cdk4/D1 (IC50= 1.2, >10 and >10 ?M). Also, potently inhibits several kinases at 1 ?M in a 25-kinase screening panel (100%, 100%, 96%, 88%, 87% and 84% against Lck, PHK, AMPK, MKK1, MAPKAP-K1 and Chk1, respectively). Reported to reduce histone H3-Ser10phosphorylation, inhibit cytokinesis, promote chromosome biorientation, perturb mitosis and polyploidy in mammalian cells. Recently shown to potently inhibit MST4 kinase (IC50= 6.18 nM) in an ATP-competitive manner. Dose-dependently accelerates hypoxia-induced apoptosis and decreases survival (EC50= 10 nM in MST4 LβT2 gonadotrope cells).
A cell-permeable indolinone compound that interacts with both the ATP- and the adjacent hydrophobic binding pocket of Aurora B and acts as a rapid and reversible inhibitor of Aurora kinase B activity (IC50~250 nM) with moderate selectivity over Cdk1/B, Cdk2/E and Cdk4/D1 (IC50= 1.2, >10 and >10 ?M). Also, potently inhibits several kinases at 1 ?M in a 25-kinase screening panel (100%, 100%, 96%, 88%, 87% and 84% against Lck, PHK, AMPK, MKK1, MAPKAP-K1 and Chk1, respectively). Reported to reduce histone H3-Ser10phosphorylation, inhibit cytokinesis, promote chromosome biorientation, perturb mitosis and polyploidy in mammalian cells.

包装

5 mg in Glass bottle
Packaged under inert gas

警告

Toxicity: Regulatory Review (Z)

重悬

Following reconstitution, aliquot freeze at -(20°C). Stock solutions are stable for up to 6 months at -20°C..

其他说明

Xiong, W., et al. 2016.Mol. Cancer Ther.15,In press.
Knowlton, A.L., et al. 2006.Curr. Biol.16,1705.
Kapoor, T.M., et al. 2006.Science311,388.
Hirota, T., et al. 2005.Nature438,1176.
Sessa, F., et al. 2005.Mol. Cell.18,379.
Lampson, M.A., et al. 2004.Nat. Cell Biol.6,232.
Hauf, S., et al. 2003.J. Cell Biol.161,281.

法律信息

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

基本信息

经验(实验)分子式 C29H32N4O3S
分子量 516.65

半岛bd体育手机客户端 性质

质量水平 100
测定 ≥95% (HPLC)
形式 solid
manufacturer/tradename Calbiochem?
储存条件 OK to freeze
protect from light
颜色 yellow
溶解性 DMSO: 50 mg/mL
运输 ambient
储存温度 ?20℃

安全信息

储存分类代码 11 - Combustible Solids
WGK WGK 2
闪点(F) Not applicable
闪点(C) Not applicable

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