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merck millipore,默克密理博,382185,HDAC Inhibitor XXII, NCH51 - CAS 848354-66-5 - Calbiochem
产品名称:HDAC Inhibitor XXII, NCH51 - CAS 848354-66-5 - Calbiochem
产品型号:382185
The HDAC Inhibitor XXII, NCH51, also referenced under CAS 848354-66-5, controls the biological activity of HDAC. This small molecule/inhibitor is primarily used for Cell Structure applications.
merck millipore,默克密理博,382185,HDAC Inhibitor XXII, NCH51 - CAS 848354-66-5 - Calbiochem
- 产品介绍
重要规格表
经验配方 CAS号 C₂₀H₂₆N₂O₂S₂ 848354-66-5 描述 概述 A cell-permeable S-isobutyryl prodrug that is processed intracellularly to form the potent HDAC inhibitor NCH-31 (IC 50 = 48 and 170 nM, respectively, using partially purified HDAC1 or HeLa nuclear extract) that is predicted to exhibit a similar HADC binding mode as that of SAHA with its sulfhydryl replacing SAHA's hydroxamate as the active-site zinc-targeting group. NCH-51 is shown to exhibit comparable antiproliferative (mean IC50 = 3.8 µM vs. 3.7 µM for SAHA; 48 h treatment) and apoptotic activity as SAHA against various cancer cell lines, but not PBMCs from 4 healthy individuals (IC50 >30 µM with either drug), and the antioxidant N-Acetyl-L-Cysteine (NAC; Cat. No. 106425) at 2 mM is reported to abolish the cell-growth inhibition caused by either 3 µM NCH-51 or SAHA in the Multiple Myeloma U266 cultures. Half-life in human plasma at 37 °C = 24 h. 产品目录编号 382185 品牌系列 Calbiochem®
同义词 Thioisobutyric acid (S-(6-(4-phenyl-2-thiazolylcarbamoyl)hexyl) ester 参考 参考 Sanda, T., et al. 2007. Leukemia 21, 2344.
Suzuki, T., et al. 2007. Bioorg. Med. Chem. Lett. 17, 1558.
Suzuki, T., et al. 2005. J. Med. Chem. 48, 1019.产品信息 CAS号 848354-66-5 形式 White powder Hill配方 C₂₀H₂₆N₂O₂S₂ 化学配方 C₂₀H₂₆N₂O₂S₂ Molar Mass 390.6 结构配方图像 生物信息 纯度 ≥97% by HPLC 理化信息 溶解度 DMSO 储存和货运信息 货运代码 Shipped with Blue Ice or with Dry Ice
毒性 Regulatory Review
储存 -20°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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