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

被引:38
作者
Li, Peng
Liu, Hong-Min [1 ]
机构
[1] Zhengzhou Univ, Coinnovat Ctr Henan Prov New Drug R&D & Preclin S, Key Lab Adv Technol Drug Preparat Technol, Minist Educ, 100 Kexue Ave, Zhengzhou 450001, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
USP7; Ubiquitination; Inhibitors; SAR; Cancer; SMALL-MOLECULE INHIBITOR; ENDOPLASMIC-RETICULUM STRESS; UV-SENSITIVE SYNDROME; CELL-CYCLE ARREST; DEUBIQUITINATING ENZYME; BIOLOGICAL EVALUATION; STRUCTURAL BASIS; DUAL INHIBITORS; ACTIVE-SITE; P53;
D O I
10.1016/j.ejmech.2020.112107
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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. (c) 2020 Elsevier Masson SAS. All rights reserved.
引用
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页数:54
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