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

Med Chem. 2013 Dec;9(8):1085-90. doi: 10.2174/1573406411309080010.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antifungal Agents / chemical synthesis
  • Antifungal Agents / chemistry*
  • Antifungal Agents / pharmacology*
  • Antifungal Agents / toxicity
  • Aspergillus niger / drug effects
  • Candida / drug effects
  • Dose-Response Relationship, Drug
  • Fibroblasts / drug effects*
  • Mice
  • Microbial Sensitivity Tests
  • Molecular Structure
  • NIH 3T3 Cells
  • Structure-Activity Relationship
  • Triazoles / chemical synthesis
  • Triazoles / chemistry
  • Triazoles / pharmacology*
  • Triazoles / toxicity*
  • Trichophyton / drug effects

Substances

  • Antifungal Agents
  • Triazoles