Homo- and hetero-dimers of inactive organophosphorous group binding at dual sites of AChE

文献类型： 外文期刊

第一作者： Zhao, Qianfei

作者： Zhao, Qianfei;Xie, Ruliang;Zhang, Tao;Mei, Xiangdong;Ning, Jun;Fang, Jing;Tang, Yun

作者机构：

关键词： AChE;Dual-site;Homo- and hetero-dimer;AChE inhibiting potency;Organophosphorous insecticide

期刊名称：BIOORGANIC & MEDICINAL CHEMISTRY LETTERS （ 影响因子：2.823； 五年影响因子：2.677 ）

ISSN： 0960-894X

年卷期： 2011 年 21 卷 21 期

页码：

收录情况： SCI

摘要： Homo- and hetero-dimers of inactive organophosphorous group(s) dramatically enhanced the acetylcholinesterase (AChE; EC 3.1.1.7) inhibiting potency, with the highest potency observed at a tether length of 6 methylene groups (6d) for the homodimers, and 7 methylene groups (8e) for the heterodimers. The docking model of Drosophila melanogaster AChE suggested that 6d and 8e bound at the catalytic and peripheral sites of AChE, in which two organophosphorous groups of 6d individually oriented towards TRP83 of catalytic sites and TRP321 of peripheral sites, and phthalicimide group of 8e was appropriately arranged for a pi-pi interaction with the phenyl ring of TYR330, furthermore, the organophosphorous group introduced hydrophobic interaction with TRP83. The compounds prepared in this work demonstrated high insecticidal activity to Lipaphis erysimi and Tetranychus cinnbarinus at the concentration 300 mg/L. (C) 2011 Elsevier Ltd. All rights reserved.

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