阿卡波糖
餐后
2型糖尿病
糖尿病
医学
药理学
2型糖尿病
小分子
化学
生物化学
内分泌学
作者
Prexa Patel,Drashti Shah,Tushar Bambharoliya,Vidhi Patel,Mehul Patel,Dharti Patel,Vashisth Bhavsar,Shantilal Padhiyar,B. M. Patel,Anjali Mahavar,Riddhisiddhi Patel,Ashish Patel
出处
期刊:Medicinal Chemistry
日期:2024-01-24
卷期号:20
标识
DOI:10.2174/0115734064264591231031065639
摘要
Abstract: One of the most effective therapeutic decencies in the treatment of Type 2 Diabetes Mellitus is the inhibition of α-glucosidase enzyme, which is present at the brush border of the intestine and plays an important role in carbohydrate digestion to form mono-, di-, and polysaccharides. Acarbose, Voglibose, Miglitol, and Erniglitate have been well-known α-glucosidase inhibitors in science since 1990. However, the long synthetic route and side effects of these inhibitors forced the researchers to move their focus to innovate simple and small heterocyclic scaffolds that work as excellent α-glucosidase inhibitors. Moreover, they are also effective against the postprandial hyperglycemic condition in Type 2 Diabetes Mellitus. In this aspect, this review summarizes recent progress in the discovery and development of heterocyclic molecules that have been appraised to show outstanding inhibition of α-glucosidase to yield positive effects against diabetes.
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