A wide variety of drug-resistant microorganisms are continuously emerging, restricting the therapeutic options for common bacterial infections. Antimicrobial agents that were originally potent are now no longer helpful, due to their weak or null activity toward these antibiotic-resistant bacteria. In addition, none of the recently approved antibiotics affect innovative targets, resulting in a need for novel drugs with innovative antibacterial mechanisms of action. The essential cell division protein filamentous temperature-sensitive Z (FtsZ) has emerged as a possible target, thanks to its ubiquitous expression and its homology to eukaryotic β-tubulin. In the latest years, several compounds were shown to interact with this prokaryotic protein and selectively inhibit bacterial cell division. Recently, our research group developed interesting derivatives displaying good antibacterial activities against methicillin-resistant Staphylococcus aureus, as well as vancomycin-resistant Enterococcus faecalis and Mycobacterium tuberculosis. The aim of the present study was to summarize the structure–activity relationships of differently substituted heterocycles, linked by a methylenoxy bridge to the 2,6-difluorobenzamide, and to validate FtsZ as the real target of this class of antimicrobials.
2,6-Difluorobenzamide Inhibitors of Bacterial Cell Division Protein FtsZ : Design, Synthesis, and Structure Activity Relationships / V. Straniero, C. Zanotto, L. Straniero, A. Casiraghi, S. Duga, A. Radaelli, C. De Giuli Morghen, E. Valoti. - In: CHEMMEDCHEM. - ISSN 1860-7179. - 12:16(2017 Sep), pp. 1303-1318.
|Titolo:||2,6-Difluorobenzamide Inhibitors of Bacterial Cell Division Protein FtsZ : Design, Synthesis, and Structure Activity Relationships|
STRANIERO, VALENTINA (Corresponding)
VALOTI, ERMANNO (Corresponding)
|Parole Chiave:||2,6-difluorobenzamides; antibiotics; antimicrobial resistance; FtsZ; inhibitors; MRSA; Molecular Medicine; Pharmacology, Toxicology and Pharmaceutics (all); Organic Chemistry|
|Settore Scientifico Disciplinare:||Settore CHIM/08 - Chimica Farmaceutica|
Settore BIO/19 - Microbiologia Generale
|Data di pubblicazione:||set-2017|
|Digital Object Identifier (DOI):||http://dx.doi.org/10.1002/cmdc.201700201|
|Appare nelle tipologie:||01 - Articolo su periodico|