| Literature DB >> 26985772 |
Maria Concetta Gidaro1, Stefano Alcaro1, Daniela Secci2, Daniela Rivanera3, Adriano Mollica4, Mariangela Agamennone4, Letizia Giampietro4, Simone Carradori4.
Abstract
Candida albicans represents the most prevalent microbial population in mucosal and systemic infections, usually confined to severely immunocompromised people. Considering the increase of resistant strains and the demand for new antifungal drugs endowed with innovative mechanism of action, we performed a ligand-based virtual screening in order to identify new anti-Candida compounds. Starting from a large library of natural/semisynthetic products and several published synthesized compounds, three coumarin derivatives were discovered in silico as new hit compounds and submitted to the in vitro assay in order to confirm their predicted biological activity.Entities:
Keywords: (thiazol-2-yl)hydrazines; Candida; coumarin; ligand-based approach; virtual screening
Mesh:
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Year: 2016 PMID: 26985772 DOI: 10.3109/14756366.2016.1156103
Source DB: PubMed Journal: J Enzyme Inhib Med Chem ISSN: 1475-6366 Impact factor: 5.051