n -扩展甲硝唑类似物的4-胺和4-(α-氨基酸)衍生物的合成及活性预测

Compounds Pub Date : 2023-01-19 DOI:10.3390/compounds3010009
Justyna Żwawiak, L. Zaprutko
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引用次数: 0

摘要

氮霉素的发现为系统地寻找对厌氧原生动物有活性的药物提供了主要的推动力。如今,硝基咪唑作为治疗剂被发现了许多其他有趣的应用。这项研究获得了许多新的4-胺-5-硝基咪唑衍生物,它们具有类似于甲硝唑的结构,是最广泛用于治疗厌氧菌、原生动物和寄生虫感染的药物的特征。用预测方法分析和确认所述化合物的治疗活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and Predicted Activity of Some 4-Amine and 4-(α-Aminoacid) Derivatives of N-Expanded-metronidazole Analogues
The discovery of azomycin provided the major impulse for the systematic search for medicines showing activity against anaerobic protozoa. Nowadays, many other interesting applications have been found for nitroimidazoles as therapeutic agents. This research led to the acquisition of numerous new 4-amine-5-nitroimidazole derivatives, which have a structure analogous to metronidazole, characteristic of medicines most widely used in the treatment of anaerobic bacteria, protozoa and parasitic infections. The therapeutic activity of the described compounds is analyzed and confirmed with predictive methods.
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CiteScore
2.30
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