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经验配方 C₁₆H₂₀ClF₃N₄O₄ 描述 概述 A cell-permeable compound that acts as a pan PAD inhibitor (IC50 = 0.8 µM, 6.2 µM and 5.9 µM for PAD1, PAD3, and PAD4, respectively) in enzymatic assays. It preferentially inactivates the calcium bound form of PAD4 in an irreversible manner, and is shown to complete with BAEE for the active site residue of this enzyme. A small but significant reduction in the efficiency of p300GDB-GRIP1 interaction is observed in transiently transfected CV-1 cells treated with Cl-amidine at concentrations between 25 µM and 200 µM, in vivo . Furthermore, this compound (200 µM) together with HDAC inhibitor SAHA (0.4 µM) has shown additive effects in inducing p21, GADD45, and PUMA expression and inhibiting cancer cell growth in a p53-dependent manner in U2OS cells. 产品目录编号 506282 品牌系列 Calbiochem®
同义词 N-α-benzoyl-N5-(2-chloro-1-iminoethyl)-L-Orn amide 参考 参考 Knuckley, B., et al. 2010. Biochemistry 23, 4852.
Li, P., et al. 2010. Oncogene 21, 3153.
Luo, Y., et al. 2006. Biochemistry 39, 11727.产品信息 形式 White solid Hill配方 C₁₆H₂₀ClF₃N₄O₄ 化学配方 C₁₆H₂₀ClF₃N₄O₄ Molar Mass 424.8 结构配方图像 生物信息 纯度 >95% 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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