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merck millipore,默克密理博,420099,JAK Inhibitor I - CAS 457081-03-7 - Calbiochem
产品名称:JAK Inhibitor I - CAS 457081-03-7 - Calbiochem
产品型号:420099
The JAK Inhibitor I, also referenced under CAS 457081-03-7, controls the biological activity of JAK. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation application More>>
merck millipore,默克密理博,420099,JAK Inhibitor I - CAS 457081-03-7 - Calbiochem
- 产品介绍
重要规格表
经验配方 CAS号 C₁₈H₁₆FN₃O 457081-03-7 描述 概述 A potent, reversible, cell-permeable, and ATP-competitive inhibitor of Janus protein tyrosine kinases (JAKs). Displays potent inhibitory activity against JAK1 (IC50 = 15 nM for murine JAK1), JAK2 (IC50 = 1 nM), JAK3 (Ki = 5 nM), and Tyk2 (IC50 = 1 nM). Inhibits other kinases at much higher concentrations. Shown to inhibit IL2- and IL4-dependent proliferation of CTLL cells and block the phosphorylation of STAT5; and further induce growth inhibition of multiple myeloma cells expressing activated JAKs and STAT3, unlike AG 490 (Cat. No. 658401). A 10 mM (500 µg/162 µl) solution of JAK Inhibitor I (Cat. No. 420097) in DMSO is also available. 产品目录编号 420099 品牌系列 Calbiochem®
同义词 2-(1,1-Dimethylethyl)-9-fluoro-3,6-dihydro-7H-benz[h]-imidaz[4,5-f]isoquinolin-7-one, Pyridone 6, P6, DBI, JAK1 Inhibitor I, JAK2 Inhibitor I, JAK3 Inhibitor X 参考 参考 Pedranzini, L., et al. 2006. Cancer Res. 66, 9714.
Lucet, I.S., et al. 2005. Blood 107, 176.
Thompson, J.E., et al. 2002. Bioorg. Med. Chem. Lett. 12, 1219.产品信息 CAS号 457081-03-7 具有ATP竞争性 Y 形式 Off-white solid Hill配方 C₁₈H₁₆FN₃O 化学配方 C₁₈H₁₆FN₃O Molar Mass 309.3 可逆 Y 结构配方图像 生物信息 主靶 murine JAK1 主靶IC50 15 nM against murine JAK1; 1 nM against JAK2; 1 nM against Tyk2 主靶Ki 5 nM against JAK3 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 -20°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 3 months at -20°C. 包装信息 惰性气体下包装 Packaged under inert gas
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