黄酮醇
化学
黄酮类
多酚
淀粉酶
生物化学
类黄酮
消化(炼金术)
对接(动物)
酶
餐后
淀粉
活动站点
α-淀粉酶
立体化学
抗氧化剂
色谱法
医学
护理部
胰岛素
内分泌学
作者
Elena Lo Piparo,Holger Scheib,Nathalie Frei,Gary Williamson,Martin Grigorov,Chieh Jason Chou
摘要
In this study we investigated the structural requirements for inhibition of human salivary alpha-amylase by flavonoids. Four flavonols and three flavones, out of the 19 flavonoids tested, exhibited IC50 values less than 100 microM against human salivary alpha-amylase activity. Structure-activity relationships of these inhibitors by computational ligand docking showed that the inhibitory activity of flavonols and flavones depends on (i) hydrogen bonds between the hydroxyl groups of the polyphenol ligands and the catalytic residues of the binding site and (ii) formation of a conjugated pi-system that stabilizes the interaction with the active site. Our findings show that certain naturally occurring flavonoids act as inhibitors of human alpha-amylase, which makes them promising candidates for controlling the digestion of starch and postprandial glycemia.
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