| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1256118 | Chinese Chemical Letters | 2007 | 4 Pages |
Abstract
Based on the active site of Candida albicans lanosterol 14α-demethylase (CACYP51), novel triazole compounds structurally different from the current triazole drugs were designed and synthesized. In vitro antifungal activities showed that compounds 10, 11, 16 and 20 exhibited strong activities. In addition, compounds 10, 11 and 16 also displayed certain activities against fluconazole-resistant fungi.
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Authors
Qiu Qin He, Ke Li, Yong Bing Cao, Huan Wen Dong, Li Hua Zhao, Chao Mei Liu, Chun Quan Sheng,