Department of Pharmacology, School of Biomedical Sciences, Faculty of Medicine and Health, University of New South Wales, Sydney, NSW 2052, Australia.
School of Pharmacy and Pharmacology, College of Health and Medicine, University of Tasmania, Hobart, TAS 7001, Australia.
Curr Drug Targets. 2023;24(8):648-661. doi: 10.2174/1389450124666230503120930.
Targeting sodium-dependent glucose transporters (SGLT1 and SGLT2) represents a new class of pharmacotherapy for type 2 diabetes mellitus, a major global health issue with an increasing social and economic burden. Following recent successes in market approvals of SGLT2 inhibitors, the ongoing effort has paved the way for the discovery of novel agents via structure-activity relationship studies, preclinical and clinical testing, including SGLT2 inhibitors, SGLT1/2 dual inhibitors, and selective SGLT1 inhibitors. A growing understanding of the physiology of SGLTs allows drug developers to explore additional cardiovascular and renal protective benefits of these agents in T2DM patients at risk. This review provides an overview of the recent investigational compounds and discusses future perspectives of drug discovery in this area.
靶向钠依赖型葡萄糖转运蛋白(SGLT1 和 SGLT2)代表了 2 型糖尿病治疗的一类新的药物疗法,这是一个日益严重的全球性健康问题,给社会和经济带来了越来越大的负担。最近 SGLT2 抑制剂在市场获批方面取得了成功,这一持续的努力为通过结构-活性关系研究、临床前和临床测试发现新型药物铺平了道路,包括 SGLT2 抑制剂、SGLT1/2 双重抑制剂和选择性 SGLT1 抑制剂。对 SGLTs 生理学的深入了解使药物开发者能够探索这些药物在有风险的 2 型糖尿病患者中的额外心血管和肾脏保护作用。本文综述了最近的研究化合物,并讨论了该领域药物发现的未来前景。