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merck millipore,默克密理博,435930,LIM Kinase Inhibitor I, LIMKi 3 - Calbiochem
产品名称:LIM Kinase Inhibitor I, LIMKi 3 - Calbiochem
产品型号:435930
The LIM Kinase Inhibitor I, LIMKi 3 controls the biological activity of LIM Kinase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.
merck millipore,默克密理博,435930,LIM Kinase Inhibitor I, LIMKi 3 - Calbiochem
- 产品介绍
重要规格表
经验配方 C₁₇H₁₄Cl₂F₂N₄OS 描述 概述 A cell-permeable pyrazolylthiazolo-isobutyramide compound that acts as a potent LIM kinase inhibitor (IC50 = 7 and 8 nM against LIMK1 and LIMK2, respectively) and effectively suppresses cellular cofilin phosphorylation (IC50 ~ 1 µM in A549 and MDA-MB-231 cultures) without affecting tubulin polymerization or inducing cytotoxicity (EC50 >10 µM in A549 proliferation & colony formation assays). Shown to effectively destabilize F-actin structure in MDA-MB-231 breast cancer cells (3 to 10 µM) with concomitant blockage of invasion (by 93% at 10 µM). 产品目录编号 435930 品牌系列 Calbiochem®
同义词 N-(5-(1-(2,6-Dichlorophenyl)-3-(difluoromethyl)-1H-pyrazol-5-yl)thiazol-2-yl)isobutyramide 参考 参考 Scott, R.W., et al. 2010. J. Cell. Biol. 191, 169.
Ross-Macdonald, P., et al. 2008. Mol. Cancer Ther. 7, 3490.产品信息 形式 Beige powder Hill配方 C₁₇H₁₄Cl₂F₂N₄OS Molar Mass 431.3 可逆 Y 结构配方图像 生物信息 主靶 LIMK1 and LIMK2 主靶IC50 7 and 8 nM against LIMK1 and LIMK2, respectively 副靶 AMPKA1, AMPKA2, DDR1, PAK3, DCAMKL2 纯度 ≥95% by HPLC 理化信息 细胞可渗透 Y 溶解度 DMSO 储存和货运信息 货运代码 Ambient Temperature Only
毒性 Standard Handling
储存 +2°C to +8°C
避光 Protect from light
无需冷冻 No
特殊指南 Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C. 包装信息 惰性气体下包装 Packaged under inert gas
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