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PubMed 25155913


Referenced in: none

Automatically associated channels: Kv11.1



Title: Optimization of physicochemical properties and safety profile of novel bacterial topoisomerase type II inhibitors (NBTIs) with activity against Pseudomonas aeruginosa.

Authors: Folkert Reck, David E Ehmann, Thomas J Dougherty, Joseph V Newman, Sussie Hopkins, Gregory Stone, Nikunj Agrawal, Paul Ciaccio, John McNulty, Herbert Barthlow, Jennifer O'Donnell, Kosalaram Goteti, John Breen, Janelle Comita-Prevoir, Mark Cornebise, Mark Cronin, Charles J Eyermann, Bolin Geng, Greg R Carr, Lakshmipathi Pandarinathan, Xuejun Tang, Andrew Cottone, Liang Zhao, Natascha Bezdenejnih-Snyder

Journal, date & volume: Bioorg. Med. Chem., 2014 Oct 1 , 22, 5392-409

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/25155913


Abstract
Type II bacterial topoisomerases are well validated targets for antimicrobial chemotherapy. Novel bacterial type II topoisomerase inhibitors (NBTIs) of these targets are of interest for the development of new antibacterial agents that are not impacted by target-mediated cross-resistance with fluoroquinolones. We now disclose the optimization of a class of NBTIs towards Gram-negative pathogens, especially against drug-resistant Pseudomonas aeruginosa. Physicochemical properties (pKa and logD) were optimized for activity against P. aeruginosa and for reduced inhibition of the hERG channel. The optimized analogs 9g and 9i displayed potent antibacterial activity against P. aeruginosa, and a significantly improved hERG profile over previously reported analogs. Compound 9g showed an improved QT profile in in vivo models and lower clearance in rat over earlier compounds. The compounds show promise for the development of new antimicrobial agents against drug-resistant Pseudomonas aeruginosa.