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CAS: 1638-41-1
分子式: C12H4Cl6O4S
分子量: 456.9
中文名称: 
p38 map 激酶抑制剂 iv
2,2′-sulfonyl-bis-(3,4,6-trichlorophenol)
2,2'-硫酰氨基-双-(3,4,6-三氯苯酚)
英文名称: 
p38 map kinase inhibitor iv
mt4
b10
用途: p38 MAPK inhibitor IV is an ATP-competitive inhibitor of p38 MAPK with IC50 values of 0.13, 0.55, 5.47, and 8.63 μM for p38α, p38β, p38, and p38δ, respectively.
推荐供应商
货号品牌产品名称规格包装、参考价格详情
M911796MACKLINp38 MAPK Inhibitor IV≥98%1157元/5mg;   展开
储存:-20°C,密闭,干燥
SML0543Sigma-Aldrichp38 MAP Kinase Inhibitor IV≥98% (HPLC)1156.54元/5 MG;   展开

产品说明

应用

p38 MAP激酶抑制剂IV被用于替代p38α激酶的激活,以检测HOXB7是否通过AKT / MAPK信号参与转移迁移和增殖过程。

包装

5, 25 mg in glass bottle

生化/生理作用

p38 MAP激酶抑制剂IV是p38α/βMAPK的ATP竞争性抑制剂,p38α和p38β的 MAPK IC50值分别为130 nM和550 nM。在1μM时,它对p38γ/σ,ERK1/2和JNK1/2/3的活性浓度、抑制率≤23%。在抑制LPS诱导hPBMC释放IL-1β方面,它比SB 203580更有效(100%vs、100μM抑制剂的抑制毒性50%)。最近的一项研究表明,p38 MAP激酶抑制剂IV可以持续显着着地增强体细胞的重编程和iPS细胞生成。

特点和优势

该化合物出现在受体分类和信号转导手册的 MAPKs页。要浏览手册其他页,点击此处。

基本信息

经验(实验)分子式C12H4Cl6O4S
分子量456.94

产品性质

质量水平100
测定≥98% (HPLC)
形式powder
颜色 white to beige
溶解性DMSO: 5 mg/mL, clear (warmed)
储存温度2-8℃

安全信息

储存分类代码13 - Non Combustible Solids
WGKWGK 3
闪点(F)Not applicable
闪点(C)Not applicable
506153Sigma-Aldrichp38 MAP Kinase Inhibitor IV-CAS 1638-41-1-CalbiochemThe p38 MAP Kinase Inhibitor IV, also referenced under CAS 1638-41-1, controls the biological activity of p38 MAP Kinase. This small molecule/inhibitor is primarily used for Phosphorylation & Deph2950.71元/10 MG;   展开

产品说明

一般描述

A cell-permeable symmetrical sulfone compound that acts as a potent and ATP-competitive inhibitor of p38α/β MAPK (IC50 = 130 and 550 nM, respectively), while exihibiting much reduced activity (≤23% inhibition at 1 µM) against p38γ/δ, ERK1/2, and JNK1/2/3. Shown to be more effective than SB 203850 (Cat. Nos. 559389, 559395, and 559398) in inhibiting LPS-induced IL-1β release from hPBMC (100% vs. 50% inhibition with 100 µM respective inhibitor).
A cell-permeable symmetrical sulfone compound that acts as a potent and ATP-competitive inhibitor of p38α/β MAPK (IC50 = 130 and 550 nM, respectively), while exihibiting much reduced activity (≤23% inhibition at 1 µM) against p38γ/δ, ERK1/2, and JNK1/2/3. Shown to be more effective than SB 203850 (Cat. Nos. 559389, 559395, and 559398) in inhibiting LPS-induced IL-1β release from hPBMC (100% vs. 50% inhibition with 100 µM respective inhibitor).

包装

10 mg in Plastic ampoule
Packaged under inert gas

警告

Toxicity: Harmful (C)

重悬

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

其他说明

Liu, Y.C., et al. 2007. Biochem. Biophys. Res. Commun.352, 656.

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C12H4Cl6O4S
分子量456.94

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
desiccated (hygroscopic)
protect from light
颜色light yellow
溶解性DMSO: 4.5 mg/mL
运输ambient
储存温度2-8℃

安全信息

储存分类代码11 - Combustible Solids
WGKWGK 3
闪点(F)Not applicable
闪点(C)Not applicable
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