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合成、抗菌及某些新型咪唑类似物的潜在抗 HIV 活性。

Synthesis, antibacterial and potential anti-HIV activity of some novel imidazole analogs.

机构信息

Department of Pharmaceutical Sciences, Birla Institute of Technology, Mesra Ranchi-835215, Jharkhand, India.

出版信息

Acta Pharm. 2011 Jun;61(2):187-201. doi: 10.2478/v10007-011-0018-2.

Abstract

A series of 1-(2-methyl-4-nitro-imidazol-1-yl)-3-arylaminopropan-2-ones (2a-e), 2-methyl-5-nitro-1-{2-[arylmethoxy]ethyl}-1H-imidazoles (5a-d), and N-(3-hydroxyphenyl)-2-(substituted imidazol-1-yl)alkanamides (8a-e) were synthesized with the aim to develop novel imidazole analogs with broad-spectrum chemotherapeutic properties. Title compounds were evaluated for their anti-HIV and antibacterial activities.

摘要

一系列 1-(2-甲基-4-硝基-1H-咪唑-1-基)-3-(芳基氨基)丙-2-酮(2a-e)、2-甲基-5-硝基-1-{2-[芳基甲氧基]乙基}-1H-咪唑(5a-d)和 N-(3-羟基苯基)-2-(取代咪唑-1-基)烷酰胺(8a-e)被合成,目的是开发具有广谱化疗特性的新型咪唑类似物。标题化合物被评估了它们的抗 HIV 和抗菌活性。

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