| Literature DB >> 25856229 |
Serena Massari1, Giulio Nannetti2, Jenny Desantis1, Giulia Muratore2, Stefano Sabatini1, Giuseppe Manfroni1, Beatrice Mercorelli2, Violetta Cecchetti1, Giorgio Palù2, Gabriele Cruciani3, Arianna Loregian2, Laura Goracci3, Oriana Tabarrini1.
Abstract
In continuing our efforts to identify small molecules able to disrupt the interaction of the polymerase acidic protein-basic protein 1 (PA-PB1) subunits of influenza virus (Flu) RNA-dependent RNA polymerase, this paper is devoted to the optimization of a dihydrotriazolopyrimidine derivative, previously identified through structure-based drug discovery. The structure modifications performed around the bicyclic core led to the identification of compounds endowed with both the ability to disrupt PA-PB1 subunits interaction and anti-Flu activity with no cytotoxicity. Very interesting results were obtained with the hybrid molecules 36 and 37, designed by merging some peculiar structural features known to impart PA-PB1 interaction inhibition, with compound 36 that emerged as the most potent PA-PB1 interaction inhibitor (IC50 = 1.1 μM) among all the small molecules reported so far. Calculations showed a very favored H-bonding between the 2-amidic carbonyl of 36 and Q408, which seems to justify its potent ability to interfere with the interaction of the polymerase subunits.Entities:
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Year: 2015 PMID: 25856229 DOI: 10.1021/acs.jmedchem.5b00012
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446