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merck millipore,默克密理博,572632,SU5614 - CAS 186611-56-3 - Calbiochem
产品名称:SU5614 - CAS 186611-56-3 - Calbiochem
产品型号:572632
A potent, cell-permeable, reversible, ATP-competitive, and selective inhibitor of VEGF (Flk-1; IC₅₀ = 1.2 µM) and PDGF (IC₅₀ = 2.9 µM) receptor tyrosine kinases.
merck millipore,默克密理博,572632,SU5614 - CAS 186611-56-3 - Calbiochem
- 产品介绍
重要规格表
经验配方 CAS号 C₁₅H₁₃N₂OCl 186611-56-3 描述 概述 A potent, cell-permeable, reversible, ATP-competitive, and selective inhibitor of VEGF (Flk-1; IC50 = 1.2 µM) and PDGF (IC50 = 2.9 µM) receptor tyrosine kinases. Does not have any effect on the EGF and IGF receptor tyrosine kinases. Also inhibits the VEGF-driven mitogenesis of human umbilical vein endothelial cells (HUVECs; IC50 ≤ 680 nM). Inhibits Flt3 phosphorylation in Flt3/Itd-BaF3 cells. 产品目录编号 572632 品牌系列 Calbiochem®
同义词 5-Chloro-3-[(3,5-dimethylpyrrol-2-yl)methylene]-2-indolinone, VEGFR Tyrosine Kinase Inhibitor VII, VEGFR2 Kinase Inhibitor IX 参考 参考 Cools, J., et al. 2004. Cancer Res. 64, 6385.
Sun, L., et al. 1998. J. Med. Chem. 41, 2588.产品信息 CAS号 186611-56-3 具有ATP竞争性 Y 声明 Not available for sale in the United States. 形式 Orange-red solid Hill配方 C₁₅H₁₃N₂OCl 化学配方 C₁₅H₁₃N₂OCl Molar Mass 272.7 可逆 Y 结构配方图像 生物信息 主靶 VEGF Flk-1 主靶IC50 1.2 µM, 2.9 µM against VEGF (Flk-1) and PDGF receptor tyrosine kinases, respectively; ≤680 nM against the VEGF-driven mitogenesis of human umbilical vein endothelial cells (HUVECs) 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 2 months at -20°C.
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