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基于 CERMN 化学库的虚拟筛选发现新型乙酰胆碱酯酶抑制剂

Virtual screening discovery of new acetylcholinesterase inhibitors issued from CERMN chemical library.

机构信息

Centre d'Etudes et de Recherche sur le Medicament de Normandie, UPRES EA-4258, FR CNRS INC3M, Universite de Caen, UFR des Sciences Pharmaceutiques, boulevard Becquerel, Caen Cedex, France.

出版信息

J Chem Inf Model. 2010 Mar 22;50(3):422-8. doi: 10.1021/ci900491t.

Abstract

In our quest to find new inhibitors able to inhibit acetylcholinesterase (AChE) and, at the same time, to protect neurons from beta amyloid toxicity, i.e., inhibitors interacting with the catalytic anionic subsite as well as with the peripherical anionic site of AChE, a virtual screening of the Centre d'Etudes et de Recherche sur le Medicament de Normandie (CERMN) chemical library was carried out. Two complementary approaches were applied, i.e., a ligand- and a structure-based screening. Each screening led to the selection of different compounds, but only two were present in both screening results. In vitro tests on AChE showed that one of those compounds presented a very good inhibition activity, of the same order as Donepezil. This result shows the real complementary of both methods for the discovery of new ligands.

摘要

在寻找新的抑制剂以抑制乙酰胆碱酯酶(AChE)并同时保护神经元免受β淀粉样毒性的过程中,即寻找与催化阴离子部位以及 AChE 的外周阴离子部位相互作用的抑制剂,我们对诺曼底药物研究与开发中心(CERMN)化学库进行了虚拟筛选。应用了两种互补的方法,即配体和基于结构的筛选。每种筛选都导致选择了不同的化合物,但只有两种化合物同时出现在两种筛选结果中。对 AChE 的体外测试表明,其中一种化合物表现出非常好的抑制活性,与多奈哌齐相当。该结果表明,这两种方法在发现新配体方面具有真正的互补性。

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