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Identification, characterization, kinetics, and molecular docking of flavonoid constituents from Archidendron clypearia (Jack.) Nielsen leaves and twigs

机译:来自archidendron clypearia(千斤顶)的黄酮类化合物(千斤顶)的鉴定,表征,动力学和分子对接尼尔森叶和树枝

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摘要

In our search for natural soluble epoxide hydrolase (sEH) inhibitors from plants, we found that the methanolic extract of the leaves and twigs of Archidendron clypearia (Jack.) Nielsen (Fabaceae) significantly inhibits sEH in vitro. In a phytochemical investigation of the water layer of A. clypearia, we isolated two new chalcones, clypesides A-B (1-2), 13 flavonoid derivatives (3-15) and established their structures based on an extensive 1D and 2D NMR, CD data, and MS analysis. All of the flavonoid derivatives inhibited sEH enzymatic activity in a dose-dependent manner, with IC50 values ranging from 10.0 +/- 0.4 to 30.1 +/- 2.1 mu M. A kinetic analysis of compounds 4, 8-10, 12, 13, and 15 revealed that the compounds 8-10 were non-competitive, 4, 13, and 15 were mixed-type, and 12 was competitive inhibitors. Additionally, molecular docking increased our understanding of their receptor-ligand binding. These results demonstrated that flavonoid derivatives from A. clypearia are potential sEH inhibitors. (C) 2016 Elsevier Ltd. All rights reserved.
机译:在我们寻找来自植物的天然可溶性环氧化物水解酶(SEH)抑制剂,我们发现archidengron植物(千斤顶)的叶片和枝条的甲醇提取物显着抑制体外SEH。在A.椰子水层的植物化学研究中,我们孤立两种新的丘氨酮,舒适的AB(1-2),13种黄酮衍生物(3-15)并基于广泛的1D和2D NMR,CD数据建立它们的结构和MS分析。所有类黄酮衍生物以剂量依赖性方式抑制SEH酶活性,IC 50值范围为10.0 +/- 0.4至30.1 +/-2.1μm。化合物4,8-10,12,13的动力学分析,图15显示化合物8-10是非竞争的,4,13和15分为混合型,12个是竞争性抑制剂。另外,分子对接增加了我们对其受体 - 配体结合的理解。这些结果表明,来自A.Clypearia的黄酮衍生物是潜在的SEH抑制剂。 (c)2016 Elsevier Ltd.保留所有权利。

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