...
首页> 外文期刊>Journal of Medicinal Chemistry >Selective 3-phosphoinositide-dependent kinase 1 (PDK1) inhibitors: Dissecting the function and pharmacology of PDK1
【24h】

Selective 3-phosphoinositide-dependent kinase 1 (PDK1) inhibitors: Dissecting the function and pharmacology of PDK1

机译:选择性3-磷酸肌醇依赖性激酶1(PDK1)抑制剂:剖析PDK1的功能和药理作用

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

3-Phosphoinositide-dependent protein kinase 1 (PDK1) is a protein target that has generated considerable interest in both academia and the pharmaceutical industry. PDK1 is responsible for regulating the activity of related kinases in the AGC kinase family, including AKT, by phosphorylating a specific threonine or serine residue within the activation loop which is critical for kinase activation. Many of the kinases activated by PDK1 regulate cellular process such as cell survival, differentiation, growth, and protein expression. Although significant work has been done to understand the role of PDK1 function in cells, recently discovered potent and selective small molecule PDK1 inhibitors are providing a unique opportunity to further dissect PDK1 function and predict the pharmacological consequences of PDK1 inhibition. This Miniperspective reviews the discovery of these selective PDK1 inhibitors and highlights their value in cellular studies, the understanding of PDK1 biology, and the impact on the therapeutic potential of PDK1 inhibition in cancer.
机译:3-磷酸​​肌醇依赖性蛋白激酶1(PDK1)是一种蛋白质靶标,在学术界和制药行业都引起了极大的兴趣。 PDK1负责通过磷酸化激活环内的特定苏氨酸或丝氨酸残基来调节AGC激酶家族(包括AKT)中相关激酶的活性,这对激酶激活至关重要。 PDK1激活的许多激酶调节细胞过程,例如细胞存活,分化,生长和蛋白质表达。尽管已经做了大量工作来了解PDK1功能在细胞中的作用,但是最近发现的有效和选择性的小分子PDK1抑制剂为进一步剖析PDK1功能和预测PDK1抑制的药理作用提供了独特的机会。本小型会议回顾了这些选择性PDK1抑制剂的发现,并强调了它们在细胞研究中的价值,对PDK1生物学的了解以及对PDK1抑制疗法在癌症中的治疗潜力的影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号