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Soluble epoxide hydrolase inhibitory components from Rheum undulatum and in silico approach

机译:来自Rheum undulatum和Silico方法的可溶性环氧化物水解酶抑制成分

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Continuous efforts to identify sEH inhibitors using activity-guided fractionation have revealed 12 known compounds, 2-13, from Rheum undulatum. Compounds 2-13 and 1, which was obtained from the in-house library, were tested for inhibitory activity against sEH. Compounds 1-9, 11, and 12 were shown to have inhibitory activity, with IC50 values ranging from 2.5 +/- 0.5 to 53.2 +/- 4.4M. They were subjected to enzyme kinetic studies to explore the binding mode between the ligand and receptor. Based on our results, compounds 1, 2, 5-9, and 11 (mixed type) and compounds 3 and 12 (noncompetitive type) had a preferred allosteric site. Compound 4 was identified as a competitive-type interaction in the active site. Molecular docking studies revealed the interacting residues and binding energy between sEH and inhibitors. Additionally, molecular dynamics provided detailed information on the interaction between the ligand and receptor.
机译:使用活性导向分级鉴定SEH抑制剂的连续努力揭示了来自Rheum undulatum的12种已知的化合物2-13。 从内部库中获得的化合物2-13和1,用于对SEH的抑制活性进行测试。 显示化合物1-9,11和12具有抑制活性,IC 50值范围为2.5 +/- 0.5至53.2 +/- 4.4m。 对它们进行酶动力学研究,以探讨配体和受体之间的结合模式。 基于我们的结果,化合物1,2,5-9和11(混合型)和化合物3和12(非竞争性型)具有优选的变构位点。 化合物4被鉴定为活性位点中的竞争型相互作用。 分子对接研究揭示了SEH和抑制剂之间的相互作用残留物和结合能。 另外,分子动力学提供了有关配体和受体之间的相互作用的详细信息。

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