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merck millipore,默克密理博,489477,LSD1 Inhibitor II, S2101 - Calbiochem
产品名称:LSD1 Inhibitor II, S2101 - Calbiochem
产品型号:489477
The LSD1 Inhibitor II, S2101 controls the biological activity of LSD1. This small molecule/inhibitor is primarily used for Cell Signaling applications.
merck millipore,默克密理博,489477,LSD1 Inhibitor II, S2101 - Calbiochem
- 产品介绍
重要规格表
经验配方 C₁₆H₁₆ClF₂NO 描述 概述 A cell-permeable, 2-PCPA derivative that elicits mechanism-based inhibition against LSD1 (IC50 = 0.99 µM, KI = 0.61 µM, and kinact/KI = 4560 M-1S-1), and displays much lower inhibition activity toward MAO-B (KI = 17 µM, kinact/KI = 18 M-1S-1) and MAO-A (KI = 110 µM, kinact/KI = 60 M-1S-1), with higher potency and selectivity compared with those of 2-PCPA (Cat. No. 616431) (IC50 = 184 µM, KI = 100 µM, kinact/KI = 58 M-1S-1 for LSD1, and K I = 26 µM, kinact/KI = 271 M-1S-1 for MAO-B, and K I = 5 µM,
kinact/KI = 1050 M-1S-1 for MAO-A). The inhibition of LSD1 is further confirmed in a cell-based assay, the treatment of HEK293T human cells with S2101 results in a dose-dependent increase in the level of H3K4me2, and about 50-fold stronger inhibition compared with that of 2-PCPA.产品目录编号 489477 品牌系列 Calbiochem®
同义词 LSD Inhibitor II, S2101, BHC110 Inhibitor II, Histone Lysine Demethylase Inhibitor IV, KDM1 Inhibitor II, MOA Inhibitor II 参考 参考 Mimasu, S., et al. 2010. Biochemistry 49, 6494. 产品信息 形式 White solid Hill配方 C₁₆H₁₆ClF₂NO 化学配方 C₁₆H₁₆ClF₂NO Molar Mass 311.75 结构配方图像 生物信息 纯度 ≥95% by HPLC 理化信息 溶解度 DMSO or H₂O 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
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.
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