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

机译:新的小分子蛋白精氨酸的细胞活性Deiminase 3(PAD3)抑制剂

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摘要

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:蛋白质精氨酸脱亚氨酶(PADs)催化精氨酸侧链的翻译后脱氨。已经表征了多种PAD同工酶,并且异常PAD活性已经与几种人类疾病状态相关联。 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,并已牵涉到脊髓损伤的神经退行性反应。在这里,我们描述了有效和选择性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拯救毒胡萝卜素诱导的表达PAD3的HEK293T细胞死亡而证明。

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