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经验配方 CAS号 C₁₃H₁₈N₂O₅S 123653-11-2 描述 概述 A cell-permeable selective inhibitor of COX-2 in vitro. Inhibits sheep placental COX-2 (IC50 = 3.8 µM) while COX-1 activity is unaffected at concentrations up to 100 µM. Displays potent anti-inflammatory and analgesic activity in vivo in rat at concentrations from 0.3 to 5 mg/kg. 产品目录编号 349254 品牌系列 Calbiochem®
同义词 N-(2-Cyclohexyloxy-4-nitrophenyl)methanesulfonamide 参考 参考 Ouellet, M., and Percival, M.D. 1995. Biochem. J. 306, 247.
Futaki, N., et al. 1994. Prostaglandins 47, 55.
Arai, I., et al. 1993. Res. Comm. Chem. Pathol. Pharmacol. 81, 259.
Futaki, N., et al. 1993. Gen. Pharmacol. 24, 105.
Futaki, N., et al. 1993. J. Pharm. Pharmacol. 45, 753.产品信息 CAS号 123653-11-2 具有ATP竞争性 N 形式 Pale yellow solid Hill配方 C₁₃H₁₈N₂O₅S 化学配方 C₁₃H₁₈N₂O₅S Molar Mass 314.4 可逆 N 结构配方图像 生物信息 主靶 COX-2 主靶IC50 3.8 µM against COX-2 纯度 ≥98% by TLC 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 +15°C to +30°C
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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