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CAS: 894804-07-0
分子式: C18H20N4O4
分子量: 356.38
英文名称: 
jnk inhibitor viii-cas 894804-07-0-calbiochem
n-(4-amino-5-cyano-6-ethoxypyridin-2-yl)-2-(2,5-dimethoxyphenyl)acetamide
用途: JNK Inhibitor VIII (TCS JNK 6o) 是 c-Jun N-末端激酶 (JNK-1, -2, -3) 抑制剂,抑制 JNK-1、JNK-2、JNK-3 的 Ki 值分别为 2 nM、4 nM、52 nM,对 JNK-1、JNK-2 的 IC50 值分别是 45 nM 和160 nM。
推荐供应商
货号品牌产品名称规格包装、参考价格详情
J797588MACKLINJNK Inhibitor VIII10mM in DMSO1304元/1ml;   展开
储存:-20°C
J876693MACKLINJNK Inhibitor VIII≥99%255元/5mg;   660元/25mg;   展开
储存:2-8℃
420135Sigma-AldrichJNK Inhibitor VIII-CAS 894804-07-0-CalbiochemThe JNK Inhibitor VIII, also referenced under CAS 894804-07-0, controls the biological activity of JNK. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation appl3543.57元/5 MG;   展开

产品说明

一般描述

A cell-permeable pyridinylamide compound that acts as an ATP-competitive, reversible inhibitor of JNK (Ki = 2 nM, 4 nM and 52 nM for JNK1, 2 and 3, respectively) and displays excellent selectivity over 72 other kinases. Inhibits c-jun phosphorylation with an EC50 of 920 nM in HepG2 cells. Preferentially blocks the growth of PTEN null mouse embryonic fibroblasts.

包装

5 mg in Plastic ampoule
Packaged under inert gas

生化/生理作用

Cell permeable: yes
Target Ki: 2 nM, 4 nM and 52 nM for JNK1, 2 and 3, respectively
Product competes with ATP.
Reversible: yes

警告

Toxicity: Standard Handling (A)

其他说明

Vivanco, I., et al. 2007. Cancer Cell11, 555.
Szczepankiewicz, B. G., et al. 2006. J. Med. Chem.49, 3563.

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C18H20N4O4
分子量356.38

产品性质

质量水平100
测定≥95% (HPLC)
形式solid
manufacturer/tradenameCalbiochem®
储存条件OK to freeze
protect from light
颜色 brown
溶解性DMSO: 10 mg/mL
运输ambient
储存温度−20℃

安全信息

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