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Synthesis of 1H-1,2,3-triazoles and study of their antifungal and cytotoxicity activities

机译:1H-1,2,3-三唑的合成及其抗真菌和细胞毒性活性的研究

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摘要

We report herein the results of antifungal activity of fifteen 1,2,3-triazoles against Candida albicans, Candida krusei, Candida parapsilosis, Candida kefyr, Candida tropicalis, Candida dubliniensis, Tricophyton rubrum, Microporum canis and Aspergillus niger. All of the 1,2,3-triazoles were prepared from 1,3-dipolar cyclizations between aryl azides and alkynes catalyzed by Cu(I), and several of the compounds exhibited antifungal activity with low cytotoxicity. The results demonstrated the potential and importance of developing new 1,2,3-triazoles compounds with antifungal activity.
机译:我们在此报告了十五种1,2,3-三唑类对白念珠菌,克鲁斯念珠菌,副念珠菌,假丝酵母​​念珠菌,热带念珠菌,杜拜念珠菌,红毛藻,小孢子菌和黑曲霉的抗真菌活性的结果。所有1,2,3-三唑均由Cu(I)催化的芳基叠氮化物和炔烃之间的1,3-偶极环化反应制备,其中一些化合物具有较低的细胞毒性,具有抗真菌活性。结果表明开发具有抗真菌活性的新的1,2,3-三唑化合物的潜力和重要性。

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