阿卡波糖
麦芽糖酶
α-葡萄糖苷酶
糖苷水解酶
化学
酶
2型糖尿病
生物化学
葡萄糖苷酶
蔗糖酶
水解
药理学
糖尿病
医学
内分泌学
作者
Lyann Sim,Kumarasamy Jayakanthan,Sankar Mohan,N. Ravindranath,Blair D. Johnston,B. Mario Pinto,David R. Rose
出处
期刊:Biochemistry
[American Chemical Society]
日期:2009-12-29
卷期号:49 (3): 443-451
被引量:132
摘要
An approach to controlling blood glucose levels in individuals with type 2 diabetes is to target alpha-amylases and intestinal glucosidases using alpha-glucosidase inhibitors acarbose and miglitol. One of the intestinal glucosidases targeted is the N-terminal catalytic domain of maltase-glucoamylase (ntMGAM), one of the four intestinal glycoside hydrolase 31 enzyme activities responsible for the hydrolysis of terminal starch products into glucose. Here we present the X-ray crystallographic studies of ntMGAM in complex with a new class of alpha-glucosidase inhibitors derived from natural extracts of Salacia reticulata, a plant used traditionally in Ayuverdic medicine for the treatment of type 2 diabetes. Included in these extracts are the active compounds salacinol, kotalanol, and de-O-sulfonated kotalanol. This study reveals that de-O-sulfonated kotalanol is the most potent ntMGAM inhibitor reported to date (K(i) = 0.03 microM), some 2000-fold better than the compounds currently used in the clinic, and highlights the potential of the salacinol class of inhibitors as future drug candidates.
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