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泛素特异性加工蛋白酶 7(USP7)抑制剂的最新研究进展。

Recent advances in the development of ubiquitin-specific-processing protease 7 (USP7) inhibitors.

机构信息

Key Laboratory of Advanced Technology of Drug Preparation Technologies, Ministry of Education, Co-innovation Center of Henan Province for New Drug R & D and Preclinical Safety, And School of Pharmaceutical Sciences, Zhengzhou University, 100 Kexue Avenue, Zhengzhou, Henan, 450001, China.

Key Laboratory of Advanced Technology of Drug Preparation Technologies, Ministry of Education, Co-innovation Center of Henan Province for New Drug R & D and Preclinical Safety, And School of Pharmaceutical Sciences, Zhengzhou University, 100 Kexue Avenue, Zhengzhou, Henan, 450001, China.

出版信息

Eur J Med Chem. 2020 Apr 1;191:112107. doi: 10.1016/j.ejmech.2020.112107. Epub 2020 Feb 1.

Abstract

Ubiquitin-specific-processing protease 7 (USP7) is one among the several deubiquitinating enzymes gaining central attention in the current cancer research. Most recent studies have focused on illustrating how USP7 is involved in the cancer process, while few articles reported the development of small molecule USP7 inhibitors. Although some review articles dealt with USP7, they mainly focused on its physiological role and not on the development of USP7 inhibitors. In this review, we systematically summarise the structures, activities and structure-activity relationship (SAR) of small molecule USP7 inhibitors, recently disclosed in scientific articles and patents from 2000 to 2019. The binding modes of typical compounds and their interactions with USP7 are also presented, while other deubiquitinase inhibitors are described in detail. Meanwhile, we briefly introduce the biochemical and physiological functions of USP7. Finally, challenges and potential strategies in developing small molecule USP7 inhibitors are also discussed.

摘要

泛素特异性蛋白酶 7(USP7)是当前癌症研究中受到广泛关注的几种去泛素化酶之一。最近的研究集中在阐明 USP7 如何参与癌症过程,而很少有文章报道小分子 USP7 抑制剂的开发。尽管一些综述文章涉及 USP7,但它们主要集中在其生理作用上,而不是 USP7 抑制剂的开发上。在这篇综述中,我们系统地总结了 2000 年至 2019 年期间在科学文献和专利中披露的小分子 USP7 抑制剂的结构、活性和构效关系(SAR)。还介绍了典型化合物的结合模式及其与 USP7 的相互作用,同时详细描述了其他去泛素化酶抑制剂。同时,我们简要介绍了 USP7 的生化和生理功能。最后,还讨论了开发小分子 USP7 抑制剂的挑战和潜在策略。

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