摘要
Twenty-one 1-(1H-1,2,4-triazolyl)-2-(2,4-diflurophenyl)-3-(4-substituted-1-piperazi nyl) -2-propanol derivatives were designed and synthesized, on the basis of the active site of lanosterol 14alpha-demethylase. In vitro antifungal activities showed that some of the target compounds had higher antifangal activity and broader antifungal spectrum than fluconazole.
- 出版日期2004-4
- 单位中国人民解放军第二军医大学