槟榔叶提取物作为抗肥胖剂对胰脂肪酶的模拟抑制作用

Mega Safithri, Nur Azizah, Maria Bintang, Rini Kurniasih
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引用次数: 0

摘要

A肥胖会引发各种退化性疾病,如中风、心脏病、2型糖尿病、胰岛素抵抗等。胰脂肪酶抑制剂是通过抑制胰脂肪酶起作用的抗肥胖药物。本研究旨在从红槟榔叶的活性化合物中寻找并预测其对胰脂肪酶的抑制活性。研究从60个测试配体的虚拟筛选、配体稳定性和毒性预测、分子对接、分子对接、二维和三维可视化验证方法开始。结果表明,基于虚拟筛选、配体稳定性、配体毒性、能量亲和力、活性位点氢键数、键距和抑制常数(Ki),辛氧乙酸苄索溴、水杨酸β - d -葡萄糖吡喃基酯和花青素对胰脂肪酶的抑制潜力最大。辛氧乙酸苄乙铵的亲和值为-8 kcal/mol,与胰脂肪酶受体(6KSM)活性位点His349残基发生氢键相互作用,键距为2,94 Å, Ki值为1,347 μM
本文章由计算机程序翻译,如有差异,请以英文原文为准。
INHIBISI EKSTRAK DAUN SIRIH MERAH TERHADAP LIPASE PANKREAS SEBAGAI ANTIOBESITAS SECARA IN SILICO
A Obesity triggers the emergence of various degenerative diseases, such as stroke, heart disease, type 2 diabetes, and insulin resistance. Pancreatic lipase inhibitors are anti-obesity drug agents that work by inhibiting pancreatic lipase enzymes. This study aims to search and predict the inhibitory activity of pancreatic lipase from the active compound of red betel leaf. The research began with virtual screening of 60 test ligands, prediction of ligand stability and toxicity, validation method of molecular docking, molecular docking, 2D and 3D visualization. The results showed that benzethonium octyloxyacetate, salicylic acid beta-D-glucopyranosyl ester, and anthocyanins had the best potential in inhibiting pancreatic lipase enzymes based on virtual screening, ligand stability, ligand toxicity, energy affinity, number of hydrogen bonds with active site, bond distance, and constants inhibition (Ki). Benzethonium octyloxyacetate has an affinity value of -8 kcal/mol, has a hydrogen bond interaction on the His349 residue on the active site of the pancreatic lipase receptor (6KSM) with a bond distance of 2,94 Å and Ki value of 1,347 μM
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