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Novel hydroxamates potentiated in vitro activity of fluconazole against Candida albicans
A set of 12 novel hydroxamate compounds (NHCs), structurally designed as inhibitors of histone deacetylase (HDAC) enzyme, were synthesized at our facility. These were adamantane derivatives with N-hydroxyacetamide as pharmacophore, and each of these compounds was tested for potentiating activity on...
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| Veröffentlicht in: | J Nat Sci Biol Med |
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| Hauptverfasser: | , , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Medknow Publications & Media Pvt Ltd
2017
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5320813/ https://ncbi.nlm.nih.gov/pubmed/28250687 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0976-9668.198349 |
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