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新型6-硝基-5-取代氨基喹啉作为局部麻醉剂和抗心律失常药物的合成及生物学评价:分子模拟研究

Synthesis and biological evaluation of novel 6-nitro-5-substituted aminoquinolines as local anesthetic and anti-arrhythmic agents: molecular modeling study.

作者信息

Goda Fatma E, Abdel-Aziz Alaa A-M, Ghoneim Hamdy A

机构信息

Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, University of Mansoura, Mansoura 35516, Egypt.

出版信息

Bioorg Med Chem. 2005 May 2;13(9):3175-83. doi: 10.1016/j.bmc.2005.02.050.

Abstract

A series of 6-nitro-5-[1-oxo-2-(substituted amino)ethylamino and 2-(substituted amino)propylamino] quinoline was synthesized and evaluated for their local anesthetic and anti-arrhythmic activity. The detailed synthesis, spectroscopic, and biological data are reported. Molecular modeling methods are used to study the local anesthetic activity of lidocaine and the active compounds by means of the AM1 method. The superposition of the stable conformations of these compounds was studied using the HyperChem 5.11 program.

摘要

合成了一系列6-硝基-5-[1-氧代-2-(取代氨基)乙基氨基和2-(取代氨基)丙基氨基]喹啉,并对其局部麻醉和抗心律失常活性进行了评估。报告了详细的合成、光谱和生物学数据。采用分子建模方法,通过AM1方法研究利多卡因和活性化合物的局部麻醉活性。使用HyperChem 5.11程序研究了这些化合物稳定构象的叠加情况。

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