1373760-88-3Relevant articles and documents
New triazole derivatives as antifungal agents: Synthesis via click reaction, in vitro evaluation and molecular docking studies
Zou, Yan,Zhao, Qingjie,Liao, Jun,Hu, Honggang,Yu, Shichong,Chai, Xiaoyun,Xu, Mingjuan,Wu, Qiuye
, p. 2959 - 2962 (2012/06/04)
A series of 1-(1H-1,2,4-triazol-1-yl)-2-(2,4-difluorophenyl)-3-substituted- 2-propanols (5a-5y) which are analogues of fluconazole, have been designed and synthesized via Cu(I)-catalyzed azide-alkyne cycloaddition on the basis of computational docking experiments to the active site of the cytochrome P450 14α-demethylase (CYP51). The in vitro antifungal activities of all the target compounds were evaluated against eight human pathogenic fungi. Compound 5l showed the best antifungal activities.