首页> 外文期刊>Mini-Reviews in Medicinal Chemistry >Xin Cao, Qi-Dong You, Zhi-Yu Li, Xiao-Jian Wang, Xiao-Yun Lu, Xiao-Rong Liu, Dan Xu, Bao Liu
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Xin Cao, Qi-Dong You, Zhi-Yu Li, Xiao-Jian Wang, Xiao-Yun Lu, Xiao-Rong Liu, Dan Xu, Bao Liu

机译:X Inc奥, Q i-dong you, Z Hi-Y UL i, ξ奥-J Ian Wang, ξ奥-Y UN l U, ξ奥-Ron GL IU, Dan X U, B AOL IU

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摘要

Src family of protein tyrosine kinases (SFKs) play key roles in regulating signal transduction in cellular processes. However, hyper-activated SFKs lead to uncontrolled cell proliferation and cancers. Many SFKs inhibitors were designed and synthesized as anticancer agents in the past several years and great progress has been made. Herein, some predominant examples of SFKs inhibitors recently developed are reviewed and special attentions are paid to the most important ATP binding site inhibitors.
机译:Src蛋白酪氨酸激酶(SFK)家族在调节细胞过程中的信号传导中起关键作用。但是,过度活化的SFK会导致不受控制的细胞增殖和癌症。在过去的几年中,许多SFKs抑制剂被设计和合成为抗癌剂,并且已经取得了很大的进展。本文中,综述了最近开发的SFKs抑制剂的一些主要实例,并特别注意了最重要的ATP结合位点抑制剂。

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