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merck millipore,默克密理博,572630,SU5402 - CAS 215543-92-3 - Calbiochem
产品名称:SU5402 - CAS 215543-92-3 - Calbiochem
产品型号:572630
A cell-permeable, reversible, and ATP-competitive inhibitor of the tyrosine kinase activity of fibroblast growth factor receptor 1 (FGFR1; IC₅₀ = 10-20 µM in the presence of 1 mM ATP).
merck millipore,默克密理博,572630,SU5402 - CAS 215543-92-3 - Calbiochem
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重要规格表
经验配方 CAS号 C₁₇H₁₆N₂O₃ 215543-92-3 描述 概述 A cell-permeable, reversible, and ATP-competitive inhibitor of the tyrosine kinase activity of fibroblast growth factor receptor 1 (FGFR1; IC50 = 10-20 µM in the presence of 1 mM ATP). Also inhibits aFGF-induced tyrosine phosphorylation of ERK1 and ERK2 (IC50 = 10-20 µM). In contrast to SU4984 (Cat. No. 572625), SU5402 is only a weak inhibitor of tyrosine phosphorylation of the PDGF receptor and does not inhibit phosphorylation of the insulin receptor. Does not inhibit the kinase activity of the EGF receptor. A 10 mM (500 µg/169 µl) solution of SU5402 (Cat. No. 572631) in DMSO is also available. 产品目录编号 572630 品牌系列 Calbiochem®
同义词 3-[3-(2-Carboxyethyl)-4-methylpyrrol-2-methylidenyl]-2-indolinone 参考 参考 Mohammadi, M., et al. 1997. Science 276, 955. 产品信息 CAS号 215543-92-3 具有ATP竞争性 Y 声明 Not available for sale in the United States. 形式 Lyophilized solid Hill配方 C₁₇H₁₆N₂O₃ 化学配方 C₁₇H₁₆N₂O₃ Molar Mass 296.3 可逆 Y 结构配方图像 生物信息 主靶 Fibroblast growth factor receptor 1 (FGFR1) 主靶IC50 10-20 &10-20 µM for fibroblast growth factor receptor 1 (FGFR1) in the presence of 1 mM ATP;M against FGFR1 in the presence of 1 mM ATP; 10-20 µM against inhibits aFGF-induced tyrosine phosphorylation of ERK1 and ERK2 纯度 ≥95% 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 (-20°C). Stock solutions are stable for up to 6 months at -20°C.
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