Synthesis of 1H-1,2,3-triazoles and Study of their Antifungal and Cytotoxicity Activities

Author(s): Iara F. da Silva, Prisicila R.C. Martins, Emanuelly G. da Silva, Sabrina B. Ferreira, Vitor F. Ferreira, Karen Regina C. da Costa, Marne C. de Vasconcellos, Emerson S. Lima, Fernando de C. da Silva

Journal Name: Medicinal Chemistry

Volume 9 , Issue 8 , 2013

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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.

Keywords: Antifungal activity, Aspergillus spp., Candida spp., cytotoxicity, Microporum canis, 1H-1, 2, 3-Triazoles, Tricophyton rubrum.

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Article Details

Year: 2013
Published on: 21 October, 2013
Page: [1085 - 1090]
Pages: 6
DOI: 10.2174/1573406411309080010
Price: $65

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