The design strategy of selective PTP1B inhibitors over TCPTP

被引:52
|
作者
Li, XiangQian
Wang, LiJun
Shi, DaYong [1 ]
机构
[1] Chinese Acad Sci, Inst Oceanol, Key Lab Expt Marine Biol, Qingdao, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Selectivity; PTP1B inhibitor; TCPTP; Diabetes; Design strategy; PROTEIN-TYROSINE-PHOSPHATASE; PHOSPHOTYROSINE BINDING-SITE; 1B INHIBITORS; ACID-DERIVATIVES; BIOLOGICAL EVALUATION; INSULIN SENSITIVITY; FOCUSED LIBRARY; CLICK CHEMISTRY; SUGAR SCAFFOLD; HUMAN-PLACENTA;
D O I
10.1016/j.bmc.2016.06.035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein tyrosine phosphatase 1B (PTP1B) has already been well studied as a highly validated therapeutic target for diabetes and obesity. However, the lack of selectivity limited further studies and clinical applications of PTP1B inhibitors, especially over T-cell protein tyrosine phosphatase (TCPTP). In this review, we enumerate the published specific inhibitors of PTP1B, discuss the structure-activity relationships by analysis of their X-ray structures or docking results, and summarize the characteristic of selectivity related residues and groups. Furthermore, the design strategy of selective PTP1B inhibitors over TCPTP is also proposed. We hope our work could provide an effective way to gain specific PTP1B inhibitors. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3343 / 3352
页数:10
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