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merck millipore,默克密理博,573132,STAT3 Inhibitor XVIII, BP-1-102 - Calbiochem
产品名称:STAT3 Inhibitor XVIII, BP-1-102 - Calbiochem
产品型号:573132
The STAT3 Inhibitor XVIII, BP-1-102 controls the biological activity of STAT3. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.
merck millipore,默克密理博,573132,STAT3 Inhibitor XVIII, BP-1-102 - Calbiochem
- 产品介绍
重要规格表
经验配方 C₂₉H₂₇F₅N₂O₆S 描述 概述 A cell-permeable, orally bioavailable amidosalicylic acid compound that selectively binds the three subpockets of Stat3 SH2 domain surface (KD = 504 nM) and blocks Stat3 phosphorylation, dimerization, and DNA-binding activity in a dose-dependent manner. Preferentially disrupts the high affinity binding between Stat3 and IL-6R/gp130-derived pTyr904 peptide (IC50 = 4.1 µM). Does not exert any significant effect on the phosphorylation status of Shc, Src, JAK1/2, Erk1/2, or Akt. Shown to reduce Stat3-dependent growth, survival, migration, and invasion of tumor cells in vitro and suppress the growth of aberrant Stat3-harboring human breast and lung tumor xenografts (3 mg/kg, i,v. or o.g.) in vivo. 产品目录编号 573132 品牌系列 Calbiochem®
同义词 4-(N-(4-Cyclohexylbenzyl)-2-(2,3,4,5,6-pentafluoro-N-methylphenylsulfonamido)acetamido)-2-hydroxybenzoic acid 参考 参考 Zhang, X., et al. Proc. Natl. Acad. Sci. USA 109, 9623. 产品信息 形式 White powder Hill配方 C₂₉H₂₇F₅N₂O₆S 化学配方 C₂₉H₂₇F₅N₂O₆S Molar Mass 626.6 可逆 Y 结构配方图像 生物信息 主靶 Stat3 纯度 ≥97% 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 3 months at -20°C. 包装信息 惰性气体下包装 Packaged under inert gas
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