| Literature DB >> 28964936 |
Rolando Cannalire1, Diana Machado2, Tommaso Felicetti1, Sofia Santos Costa2, Serena Massari1, Giuseppe Manfroni1, Maria Letizia Barreca1, Oriana Tabarrini1, Isabel Couto2, Miguel Viveiros2, Stefano Sabatini3, Violetta Cecchetti1.
Abstract
Mycobacterium avium is a difficult-to-treat pathogen able to quickly develop drug resistance. Like for other microbial species, overexpression of efflux pumps is one of the main mechanisms in developing multidrug resistance. Although the use of efflux pumps inhibitors (EPIs) represents a promising strategy to reverse resistance, to date few M. avium EPIs are known. Recently, we showed that in-house 2-phenylquinoline S. aureus NorA EPIs exhibited also a good activity against M. avium efflux pumps. Herein, we report a series of 3-phenylquinolones designed by modifying the isoflavone biochanin A, a natural EPI of the related M. smegmatis, taking into account some important SAR information obtained around the 2-phenylquinoline NorA EPIs. The 3-phenylquinolones inhibited M. avium efflux pumps with derivatives 1e and 1g that displayed the highest synergistic activity against all the strains considered in the study, bringing down (from 4- to 128-fold reduction) the MIC values of macrolides and fluoroquinolones.Entities:
Keywords: 3-Phenylquinolones; Antimicrobial resistance; Efflux pump inhibitors; M. avium complex; Nontuberculous mycobacteria
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Year: 2017 PMID: 28964936 DOI: 10.1016/j.ejmech.2017.09.014
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514