三唑/苯并咪唑杂化分子的合成、抗真菌活性及硅研究

IF 1.8 3区 化学 Q3 CHEMISTRY, ORGANIC
Ganesh Babu N. V. N. Kolukula (Methodology) , Penke Vijaya Babu (Writing – original draft) , Korripally Premsagar (Validation) , Sibbala Subramanyam (Supervision)
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引用次数: 0

摘要

利用铜催化咔嗒反应(CuAAC)合成了一系列新的三唑/苯并咪唑杂化分子。所有新合成的化合物都通过分析数据得到了很好的表征。大多数目标化合物对各种念珠菌菌株显示出潜在的抗真菌活性。特别是,化合物6a在所有浓度下对所测试的念珠菌菌株表现出最高的抗真菌活性,突出了其作为治疗剂的潜力,并且该活性得到了广泛的计算机研究的支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis, anti-fungal activities and in silico studies of triazole/benzimidazole hybrid molecules
A new series of triazole/benzimidazole hybrid molecules are synthesized using copper-catalyzed click reaction (CuAAC). All the newly synthesized compounds were well-characterized by analytical data. Most of the target compounds displayed potential anti-fungal activity against various Candida strains. In particular, compound 6a exhibited the highest antifungal activity against the tested Candida strains across all concentrations, highlighting its potential as a therapeutic agent, and the activity was supported by extensive in silico studies.
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来源期刊
Synthetic Communications
Synthetic Communications 化学-有机化学
CiteScore
4.40
自引率
4.80%
发文量
156
审稿时长
4.3 months
期刊介绍: Synthetic Communications presents communications describing new methods, reagents, and other synthetic work pertaining to organic chemistry with sufficient experimental detail to permit reported reactions to be repeated by a chemist reasonably skilled in the art. In addition, the Journal features short, focused review articles discussing topics within its remit of synthetic organic chemistry.
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