首页> 外文期刊>Molecules >Recent Advances in Developing Inhibitors for Hypoxia-Inducible Factor Prolyl Hydroxylases and Their Therapeutic Implications
【24h】

Recent Advances in Developing Inhibitors for Hypoxia-Inducible Factor Prolyl Hydroxylases and Their Therapeutic Implications

机译:缺氧诱导因子脯氨酰羟化酶抑制剂的研究进展及其治疗意义

获取原文
获取原文并翻译 | 示例
       

摘要

Hypoxia-inducible factor (HIF) prolyl hydroxylases (PHDs) are members of the 2-oxoglutarate dependent non-heme iron dioxygenases. Due to their physiological roles in regulation of HIF-1 stability, many efforts have been focused on searching for selective PHD inhibitors to control HIF-1 levels for therapeutic applications. In this review, we first describe the structure of PHD2 as a molecular basis for structure-based drug design (SBDD) and various experimental methods developed for measuring PHD activity. We further discuss the current status of the development of PHD inhibitors enabled by combining SBDD approaches with high-throughput screening. Finally, we highlight the clinical implications of small molecule PHD inhibitors.
机译:缺氧诱导因子(HIF)脯氨酰羟化酶(PHD)是2-氧戊二酸依赖性非血红素铁双加氧酶的成员。由于它们在调节HIF-1稳定性中的生理作用,因此许多努力集中在寻找选择性PHD抑制剂以控制HIF-1水平以用于治疗应用。在这篇综述中,我们首先将PHD2的结构描述为基于结构的药物设计(SBDD)的分子基础,并开发了用于测量PHD活性的各种实验方法。我们进一步讨论了通过结合SBDD方法和高通量筛选来实现PHD抑制剂的开发现状。最后,我们强调了小分子PHD抑制剂的临床意义。

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