| Literature DB >> 27304878 |
Giannamaria Annunziato1, Andrea Angeli2, Francesca D'Alba1, Agostino Bruno3, Marco Pieroni1, Daniela Vullo4, Viviana De Luca5, Clemente Capasso5, Claudiu T Supuran6,7, Gabriele Costantino1.
Abstract
In academia, compound recycling represents an alternative drug discovery strategy to identify new pharmaceutical targets from a library of chemical compounds available in house. Herein we report the application of a rational target-based drug-repurposing approach to find diverse applications for our in-house collection of compounds. The carbonic anhydrase (CA, EC 4.2.1.1) metalloenzyme superfamily was identified as a potential target of our compounds. The combination of a thoroughly validated docking screening protocol, together with in vitro assays against various CA families and isoforms, allowed us to identify two unprecedented chemotypes as CA inhibitors. The identified compounds have the capacity to preferentially bind pathogenic (bacterial/protozoan) CAs over human isoforms and represent excellent hits for further optimization in hit-to-lead campaigns.Entities:
Keywords: carbonic anhydrase; computational chemistry; drug design; enzymes; inhibitors
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Year: 2016 PMID: 27304878 DOI: 10.1002/cmdc.201600180
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466