| Literature DB >> 25381141 |
Abstract
Novel histone deacetylase inhibitors have been developed for the antifungal therapy. Molecule 8 exhibited potent antifungal activities with MIC values of 0.25/0.25, 0.12/0.25, 0.12/0.12 µg/ml against Candida albicans, C. parapsilosis and C. glabrata after 24/48 h incubation, respectively. Most of the synthesized compound showed significantly synergistic effects with fluconazole in the biological assay. The discovery of these molecules makes positive contributions to the development of potent and safe antifungal drugs.Entities:
Keywords: antifungal; histone deacetylase; inhibitor; selectivity
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Year: 2014 PMID: 25381141 DOI: 10.1517/13543776.2014.981256
Source DB: PubMed Journal: Expert Opin Ther Pat ISSN: 1354-3776 Impact factor: 6.674