An Updated Overview of Synthetic α-glucosidase Inhibitors: Chemistry and Bioactivities

被引:5
|
作者
Cai, Yong-Si [1 ]
Xie, Hong-Xu [1 ]
Zhang, Jin-He [1 ]
Li, Yue [1 ]
Zhang, Juan [1 ]
Wang, Kai-Ming [1 ]
Jiang, Cheng-Shi [1 ]
机构
[1] Univ Jinan, Sch Biol Sci & Technol, Jinan 250022, Peoples R China
关键词
alpha-glucosidase inhibitors; Heterocycles; Structure-activity relationship; Molecular docking; Diabetes mellitus; Hypoglycaemic drugs; PPAR-GAMMA AGONISTS; IN-VITRO EVALUATION; MOLECULAR DOCKING; BIOLOGICAL EVALUATION; OLEANOLIC ACID; URSOLIC ACID; BENZIMIDAZOLE DERIVATIVES; ANTIDIABETIC ACTIVITY; DIABETES-MELLITUS; DESIGN;
D O I
10.2174/0115680266260682230921054652
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Diabetes mellitus (DM) is a critical global health issue, affecting nearly half a billion people worldwide, with an increasing incidence rate and mortality. Type 2 diabetes is caused by the body's inability to effectively use insulin, and approximately 95% of patients have type 2 diabetes. alpha-glucosidase has emerged as an important therapeutic target for the treatment of type 2 diabetes. In the past years, three alpha-glucosidase inhibitors have been approved for clinical use, namely acarbose, voglibose, and miglitol. However, the undesirable effects associated with these carbohydrate mimic-based alpha-glucosidase inhibitors have limited their clinical applications. Consequently, researchers have shifted their focus towards the development of non-carbohydrate mimic alpha-glucosidase inhibitors that can safely and effectively manage postprandial hyperglycemia in type 2 diabetes. Herein, this article provides an overview of the synthetic alpha-glucosidase inhibitors, particularly those based on heterocycles, which have been reported from 2018 to 2022. This article aims to provide useful information for medicinal chemists in further developing clinically available anti-type 2 diabetes drugs.
引用
收藏
页码:2488 / 2526
页数:39
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