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Cellular Activity of New Small Molecule Protein Arginine Deiminase 3 (PAD3) Inhibitors

机译:新型小分子蛋白质精氨酸脱亚氨酶3(PAD3)抑制剂的细胞活性。

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The protein arginine deiminases (PADs) catalyze the post-translational deimination of arginine side chains. Multiple PAD isozymes have been characterized, and abnormal PAD activity has been associated with several human disease states. PAD3 has been characterized as a modulator of cell growth via apoptosis inducing factor and has been implicated in the neurodegenerative response to spinal cord injury. Here, we describe the design, synthesis, and evaluation of conformationally constrained versions of the potent and selective PAD3 inhibitor 2. The cell activity of representative inhibitors in this series was also demonstrated for the first time by rescue of thapsigargin-induced cell death in PAD3-expressing HEK293T cells.
机译:精氨酸脱亚氨酶(PADs)催化精氨酸侧链的翻译后脱氨。已经鉴定出多种PAD同工酶,并且PAD活性异常与几种人类疾病状态有关。 PAD3已被表征为通过凋亡诱导因子来调节细胞生长的调节剂,并且已被暗示对脊髓损伤的神经退行性反应。在这里,我们描述了有效的和选择性的PAD3抑制剂2的构象约束形式的设计,合成和评估。该系列中代表性抑制剂的细胞活性也首次通过thapsigargin诱导的PAD3细胞死亡的抢救得以证实。表达HEK293T细胞。

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