S.N. Lavrenov*, Simonov A. Yu, A.A. Panov, S.E. Solovieva, A.B. Mantsyzov, А.V. Churakov, A.S. Trenin and I.B. Levshin Pages 1 - 14 ( 14 )
Introduction: A new series of triazoles with antifungal activity have been synthesized in a one-step fashion by direct reaction of 2-(2,4-difluorophenyl)-2,3-epoxy- 1-(1H-1,2,4-triazol-1-yl)propane with various diamines.
Method: Obtained compounds were profiled for biological activity against pathogenic strains of fungi C. albicans and A. niger. Molecular modeling was used to predict binding modes.
Result: The lead compound was 4 times more active against C. albicans than fluconazole and demonstrated a wider spectrum of activity, inhibiting the growth of A. niger.
Conclusion: The results presented herein can contribute to the development of novel antifungal therapeutic agents.
Antifungals, azoles, homodimers, diamines.