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merck millipore,默克密理博,662086,UCH-L1 Inhibitor - CAS 668467-91-2 - Calbiochem
产品名称:UCH-L1 Inhibitor - CAS 668467-91-2 - Calbiochem
产品型号:662086
The UCH-L1 Inhibitor, also referenced under CAS 668467-91-2, controls the biological activity of UCH-L1. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.
merck millipore,默克密理博,662086,UCH-L1 Inhibitor - CAS 668467-91-2 - Calbiochem
- 产品介绍
重要规格表
经验配方 CAS号 C₁₇H₁₁Cl₃N₂O₃ 668467-91-2 描述 概述 An isatin O-acyl oxime compound that acts as a potent, reversible, competitive, and active site-directed inhibitor of UCH-L1 (Ki = 0.40 µM; IC50 = 0.88 µM) with ~28-fold greater selectivity over UCH-L3 (Cat. No. 662090). Shown to increase proliferation of UCH-L1 expresssing tumor cell line SH-SY5Y at 5 µM. A useful tool for studying the roles of UCH-L1 in cancer, Parkinson’s disease, and other neurological disorders. Permeability may vary from cell type to cell type. 产品目录编号 662086 品牌系列 Calbiochem®
同义词 LDN-57444, Ubiquitin C-Terminal Hydrolase L1 Inhibitor, Ubiquitin C-Terminal Esterase L1 Inhibitor, Ubiquitin Thiolesterase L1 Inhibitor 参考 参考 Liu, Y., et al. 2003. Chem. Biol. 10, 837. 产品信息 CAS号 668467-91-2 具有ATP竞争性 Y 形式 Orange solid Hill配方 C₁₇H₁₁Cl₃N₂O₃ 化学配方 C₁₇H₁₁Cl₃N₂O₃ Molar Mass 397.6 可逆 Y 结构配方图像 生物信息 主靶 UCH-L1 主靶IC50 0.88 µM 主靶Ki 0.40 µM 纯度 ≥95% by HPLC 理化信息 细胞可渗透 N 溶解度 DMSO 储存和货运信息 货运代码 Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
毒性 Carcinogenic / Teratogenic
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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