| Literature DB >> 30067360 |
Tommaso Felicetti1, Rolando Cannalire1, Donatella Pietrella1, Gniewomir Latacz2, Annamaria Lubelska2, Giuseppe Manfroni1, Maria Letizia Barreca1, Serena Massari1, Oriana Tabarrini1, Katarzyna Kieć-Kononowicz2, Bryan D Schindler3, Glenn W Kaatz3, Violetta Cecchetti1, Stefano Sabatini1.
Abstract
Antimicrobial resistance (AMR) represents a hot topic in drug discovery. Besides the identification of new antibiotics, the use of nonantibiotic molecules to block resistance mechanisms is a powerful alternative. Bacterial efflux pumps exert an early step in AMR development by allowing bacteria to grow at subinhibitorial drug concentrations. Thus, efflux pump inhibitors (EPIs) offer a great opportunity to fight AMR. Given our experience in developing Staphylococcus aureus NorA EPIs, in this work, starting from the 2-phenylquinoline hit 1, we planned the introduction of methoxy groups on the basis of their presence in known NorA EPIs. Among the 35 different synthesized derivatives, compounds 3b and 7d exhibited the best NorA inhibition activity by restoring at very low concentrations ciprofloxacin MICs against resistant S. aureus strains. Interestingly, both compounds displayed EPI activities at nontoxic concentrations for human cells as well as highlighted promising results by preliminary pharmacokinetic studies.Entities:
Mesh:
Substances:
Year: 2018 PMID: 30067360 DOI: 10.1021/acs.jmedchem.8b00791
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446