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首页> 外文期刊>Zeitschrift fur Naturforschung, B. A Journal of Chemical Sciences >Nitroimidazoles part 7. Synthesis and Anti-HIV activity of new 4-Nitroimidazole derivatives
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Nitroimidazoles part 7. Synthesis and Anti-HIV activity of new 4-Nitroimidazole derivatives

机译:硝基咪唑第7部分。新的4-硝基咪唑衍生物的合成和抗HIV活性

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摘要

Reverse transcriptase enzyme(RT)is an attractive target for the development of new drugs useful in AIDS therapy and HIV non-nucleoside reverse transcriptase inhibitors(NNRTIs), and offers the possibility of generating structures of increased potency. On this basis, a series of 4-oxo-3-phenyl-2-(phenylimino)thiazolidin-5-ylidene, 3-hydroxypropyl, 3-azidopropyl, and 3-aminopropyl derivatives of 1-benzyl-2-ethyl-4-nitroimidazoles 6-8, as well as the substituted 1, 2, 3-triazolo analogs 12-14, the diazepam 15 and carboxamide derivatives 16 and 17 were synthesized. All compounds have been evaluated for their anti-HIV activity.
机译:逆转录酶(RT)是开发可用于AIDS治疗的新药和HIV非核苷逆转录酶抑制剂(NNRTIs)的有吸引力的目标,并提供产生效力增强结构的可能性。在此基础上,形成了一系列的1-苄基-2-乙基-4-基的4-氧代-3-苯基-2-(苯基亚氨基)噻唑烷-5-亚烷基,3-羟丙基,3-叠氮基丙基和3-氨基丙基衍生物。合成了硝基咪唑6-8以及取代的1,2,3-三唑类似物12-14,地西epa 15和羧酰胺衍生物16和17。已经评估了所有化合物的抗HIV活性。

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