摘要
In an attempt to search for many target compounds with excellent activities, a series of vinyl ether-containing azole derivatives were designed, synthesized, and evaluated as antifungal agents. Results of preliminary antifungal tests against Trichophyton rubrum in vitro indicated that most of the synthesized compounds showed excellent activities. In comparison with fluconazole, itraconazole, voriconazole, omoconazole and amphotericin B, several compounds (such as 7d, 7g and 7h) exhibited more potent inhibitory activities, suggesting that they were promising leads for the development of novel antifungal agents.
源语言 | 英语 |
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页(从-至) | 4887-4890 |
页数 | 4 |
期刊 | Bioorganic and Medicinal Chemistry Letters |
卷 | 22 |
期 | 14 |
DOI | |
出版状态 | 已出版 - 15 7月 2012 |