Protein Phosphatases: A Neglected Target Family for Drug Discovery

被引:1
|
作者
Lewis, Joe [1 ]
Mueller, Gerhard [1 ]
机构
[1] Anavo Therapeut, JH Oortweg 19, NL-233 CH Leiden, Netherlands
关键词
Allosteric inhibitors; Inhibitors; Kinases; Phosphatases; PTP1B; SHP2; Target family; TYROSINE PHOSPHATASES; 1B INHIBITORS; STRATEGIES; SITE;
D O I
10.2533/chimia.2022.460
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The gene family of protein phosphatases is a rich but under-exploited source of therapeutically validated drug targets modulating signal transduction pathways. Unlike the kinase family, research and development activities have not yet yielded any approved small-molecule drugs against a phosphatase. Approximately 20 years ago, the phosphatase family was classified as undruggable and intractable. This was primarily due to the spectacular failure of the cumulated industry-wide drug discovery efforts to develop PTP1B inhibitors. Recently, allosteric inhibitors against SHP2, a member of the phosphatase family, have entered clinical trials, which has reawakened industry's interest towards this neglected enzyme family. This contribution reviews the recent R&D trends around small-molecule efforts towards phosphatase modulators over the last years, rather than providing an exhaustive review of the field of allosteric phosphatase inhibitors.
引用
收藏
页码:460 / 465
页数:6
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