各种香豆素类化合物治疗肥胖症的硅脂肪酶抑制活性筛选

Bui Thanh Tung, Le Thi Huong, Nguyen Thi Hong Hanh, Nguyen Hai Ha
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摘要

目前,肥胖是最常见的疾病之一,在许多国家都有很高的发病率。胰脂肪酶(PL)是胰腺分泌的主要酶,对单甘油酯和游离脂肪酸的形成有直接影响。抑制胰脂肪酶有助于分解脂肪,减少卡路里,减肥。香豆素是一组对肥胖有积极作用的化合物。因此,我们的研究旨在通过分子对接的方法来评价和筛选有效抑制脂肪酶的香豆素类化合物。结果,我们得到了8个化合物,它们的结合能值低于阳性对照奥利司他,并且在评估Lipinski五法则时满足类药物性质。之后,这些化合物继续进行药代动力学和毒理学特性(ADMET)分析,得到了三种效果最好的化合物:Peucenidin、Edultin和Xanthalin,它们肠道吸收好,组织分布均匀,经肝脏代谢,肝代谢,肾排泄,毒性低。因此,需要进一步的体内和体外研究来开发治疗肥胖的药物。
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Screening In Silico Lipase Inhibitory Activity of Various Coumarin Compounds for the Treatment of Obesity
Currently, obesity is one of the most common diseases and accounts for a high rate in many countries. Pancreatic lipase (PL) is the major enzyme secreted by the pancreas that has a direct effect on the formation of monoglycerides and free fatty acids. Inhibition of pancreatic lipase enzyme helps to break down fat, reduce kCal, and lose weight. Coumarins are a group of compounds that are active in obesity. Therefore, our study aimed to evaluate and screen coumarin compounds effective in inhibiting lipase enzyme by molecular docking method. As a result, we obtained eight compounds showing lower binding energy values than the positive control Orlistat and satisfying drug-like properties when evaluating the Lipinski rule of five. After that, these compounds continued to analyze pharmacokinetic and toxicological properties (ADMET) to obtain three compounds with the best results: Peucenidin, Edultin, and Xanthalin with good intestinal absorption, well distributed to tissues, metabolized by the liver, hepatic metabolism, renal excretion, and low toxicity. Therefore, further in vivo and in vitro studies are needed to develop drugs for the treatment of obesity.
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