950821-44-0Relevant articles and documents
Synthesis of novel triazole derivatives as inhibitors of cytochrome P450 14α-demethylase (CYP51)
Sun, Qing-Yan,Xu, Jian-Ming,Cao, Yong-Bing,Zhang, Wan-Nian,Wu, Qiu-Ye,Zhang, Da-Zhi,Zhang, Jun,Zhao, Hui-Qing,Jiang, Yuan-Ying
, p. 1226 - 1233 (2007)
A series of 1-(1H-1,2,4-triazol-1-yl)-2-(2,4-difluorophenyl)-3-[(4-substitutedphenyl)-piperazin-1-yl]-propan-2-ols have been designed and synthesized on the basis of the structure-activity relationships and antimycotic mechanism of azole antifungal agents
New azoles with antifungal activity: Design, synthesis, and molecular docking
Chai, Xiaoyun,Zhang, Jun,Cao, Yongbing,Zou, Yan,Wu, Qiuye,Zhang, Dazhi,Jiang, Yuanying,Sun, Qingyan
supporting information; experimental part, p. 686 - 689 (2011/02/27)
In order to search for many target compounds with excellent activities, a series of 1-(1H-1,2,4-triazol-1-yl)-2-(2,4-difluoro-phenyl)-3-[(4-substituted phenyl)-piperazin-1-yl]-propan-2-ols were designed, synthesized, and evaluated as antifungal agents. Re