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merck millipore,默克密理博,530389,RIPK3 Inhibitor, GSKʹ872 - Calbiochem
产品名称:RIPK3 Inhibitor, GSKʹ872 - Calbiochem
产品型号:530389
A cell-permeable, selective inhibitor of RIP3-selective kinase with >1,000-fold selectivity over a vast majority of more than 300 other kinases.
merck millipore,默克密理博,530389,RIPK3 Inhibitor, GSKʹ872 - Calbiochem
- 产品介绍
重要规格表
经验配方 C₁₉H₁₇N₃O₂S₂ 描述 概述 A cell-permeable quinolinyl-benzothiazolamine compound that is reported to act as a RIP3-selective kinase inhibitor with >1,000-fold selectivity over a vast majority of more than 300 other kinases, including RIP1. RIP1 inhibitor Nec-1 (30 µM; Cat. Nos. 480065 & 505224) can be employed in conjunction with GSK'872 (3 µM) in delineating RIP1- vs. RIP3-dependency in Toll-like receptors- (TLRs) mediated necrosis and TNFR1-initiated necroptosis in the presence or absence of caspase inhibitor Z-VAD-FMK (25 µM; Cat. Nos. 627609 & 627610). 产品目录编号 530389 品牌系列 Calbiochem®
同义词 N-(6-(Isopropylsulfonyl)quinolin-4-yl)benzo[d]thiazol-5-amine, RIP3 Kinase Inhibitor I, Receptor-Interacting Protein Kinase 3 Inhibitor I, GSK-872, Necrosis Inhibitor V, RIPK3 Inhibitor I 参考 参考 Kaiser, W.J., et al. 2013. J. Biol. Chem. 288, 31268. 产品信息 形式 Yellow solid Hill配方 C₁₉H₁₇N₃O₂S₂ 化学配方 C₁₉H₁₇N₃O₂S₂ 可逆 Y 生物信息 主靶 RIP3 Kinase 纯度 ≥98% 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 9-20°C). Stock solutions are stable for up to 3 months at -20°C. 包装信息 惰性气体下包装 Packaged under inert gas
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