Lo Piparo Elena, Scheib Holger, Frei Nathalie, Williamson Gary, Grigorov Martin, Chou Chieh Jason
Nestlé Research Center, Vers-chez-les-Blanc, PO Box 44, CH-1000 Lausanne 26, Switzerland.
J Med Chem. 2008 Jun 26;51(12):3555-61. doi: 10.1021/jm800115x. Epub 2008 May 29.
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.
在本研究中,我们调查了黄酮类化合物抑制人唾液α-淀粉酶的结构要求。在所测试的19种黄酮类化合物中,四种黄酮醇和三种黄酮对人唾液α-淀粉酶活性的IC50值小于100微摩尔。通过计算配体对接对这些抑制剂的构效关系研究表明,黄酮醇和黄酮的抑制活性取决于:(i)多酚配体的羟基与结合位点催化残基之间的氢键;(ii)形成稳定与活性位点相互作用的共轭π-体系。我们的研究结果表明,某些天然存在的黄酮类化合物可作为人α-淀粉酶的抑制剂,这使其成为控制淀粉消化和餐后血糖的有前景的候选物。