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Design, synthesis, and antifungal activities of novel triazole derivatives containing the benzyl group
In previous studies undertaken by our group, a series of 1-(1H-1,2,4-triazole-1-yl)-2-(2,4-difluorophenyl)-3-substituted-2-propanols (1a–r), which were analogs of fluconazole, was designed and synthesized by click chemistry. In the study reported here, the in vitro antifungal activities of all the t...
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| Vydáno v: | Drug Des Devel Ther |
|---|---|
| Hlavní autoři: | , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Dove Medical Press
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4362653/ https://ncbi.nlm.nih.gov/pubmed/25792806 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/DDDT.S74989 |
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