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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

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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-1α stability, many efforts have been focused on searching for selective PHD inhibitors to control HIF-1α 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-1α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-1α的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,以及为测量PHD活性而开发的各种实验方法。我们进一步讨论了通过将SBDD方法与高通量筛选相结合而实现的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。

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