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位置: 首页> 品牌> Sigma-Aldrich> 转化生长因子-βRI 激酶抑制剂 IV-CAS 909910-43-6-Calbiochem

TGF-β RI Kinase Inhibitor IV-CAS 909910-43-6-Calbiochem

转化生长因子-βRI 激酶抑制剂 IV-CAS 909910-43-6-Calbiochem

品牌
Sigma-Aldrich
CAS
909910-43-6
货号
616454
规格纯度
TGF-β RI Kinase Inhibitor IV, CAS 909910-43-6, is a cell-permeable, selective inhibitor of ALK-4/5/7-mediated signaling (IC50= 45, 12, and 7.5 nM, respectively).
价格
2741.8 *本价格含增值税费
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半岛bd体育手机客户端 名称:
909910-43-6
TGF-β RI Kinase Inhibitor IV-CAS 909910-43-6-Calbiochem
Transforming Growth Factor-β Type I Receptor Kinase Inhibitor IV, 3-(6-Methylpyridin-2-yl)-4-(4-quinolyl)-1-phenylthiocarbamoyl-1H-pyrazole, A-83-01, ALK5 Inhibitor IV
转化生长因子-βRI 激酶抑制剂 IV-CAS 909910-43-6-Calbiochem
半岛bd体育手机客户端 介绍:

半岛bd体育手机客户端 说明

一般描述

A cell-permeable trisubstituted pyrazole compound that has been shown to selectively inhibit ALK-4/5/7-mediated (IC50= 45, 12, and 7.5 nM, respectively, in luciferase transcription activity assays), but not ALK-1/2/3/6-mediated cellular signaling in Mv1Lu R4-2 transfectants expressing the individual Type I TGF-β receptors. Inhibits TGF-β-induced Smad2-phosphorylation in HaCaT cells and epithelial-to-mesenchymal transition in NMuMG cells at a concentration of 1 ?M.

包装

2 mg in Plastic ampoule
Packaged under inert gas

生化/生理作用

Cell permeable: yes
Target IC50: 45, 12, and 7.5 nM, respectively, in inhibit ALK-4/5/7-mediated luciferase transcription activity assays
Primary Target
ALK-4/5/7
Product does not compete with ATP.
Reversible: no

警告

Toxicity: Harmful (C)

重悬

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

其他说明

Tojo, M., et al. 2005.Cancer Sci.96,791.

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 C25H19N5S
分子量 421.52

半岛bd体育手机客户端 性质

质量水平 200
测定 ≥97% (HPLC)
形式 solid
manufacturer/tradename Calbiochem?
储存条件 OK to freeze
protect from light
颜色 pale yellow
溶解性 DMSO: 20 mg/mL
运输 ambient
储存温度 2-8℃

安全信息

储存分类代码 11 - Combustible Solids
WGK WGK 3

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