首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Design, synthesis, and antifungal activity of triazole and benzotriazole derivatives.
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Design, synthesis, and antifungal activity of triazole and benzotriazole derivatives.

机译:三唑和苯并三唑衍生物的设计,合成和抗真菌活性。

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摘要

This study describes the design, synthesis and evaluation of a novel series of 1,2,4-triazole and benzotriazole derivatives as inhibitors of cytochrome P450 14alpha-demethylase (14DM). The chemical structures of the new compounds were confirmed by elemental and spectral ((1)H NMR, (13)C NMR, Mass) analyses. Compounds were designed by a generating virtual library of compounds and docking them into the enzyme active site. Furthermore, they were found to have in vitro activity against Microsporum canis, Trichophyton mentagrophyte, Trichophyton rubrum, Epidermophyton floccosum, and Candida albicans comparable to fluconazole and clotrimazole.
机译:这项研究描述了一系列新型的1,2,4-三唑和苯并三唑衍生物作为细胞色素P45014α-脱甲基酶(14DM)抑制剂的设计,合成和评估。新化合物的化学结构通过元素分析和光谱分析((1)H NMR,(13)C NMR,Mass)分析得到确认。通过生成化合物的虚拟文库并将其对接到酶活性位点中来设计化合物。此外,发现它们具有与氟康唑和克霉唑相当的体外抗犬小孢子菌,薄荷毛癣菌,红毛癣菌,絮状表皮菌和白色念珠菌的体外活性。

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