Design and virtual screening of novel fluoroquinolone analogs as effective mutant DNA GyrA inhibitors against urinary tract infection-causing fluoroquinolone resistant Escherichia coli
Author:
Affiliation:
1. Drug Discovery and Development Research Group
2. Department of Pharmaceutical Technology
3. University College of Engineering
4. Anna University
5. Tiruchirapalli-62024
Abstract
Design and development of novel fluoroquinolones analogs using target (mutant DNA GyrA), ligand-based SAR and virtual screening techniques.
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2018/RA/C8RA01854E
Reference40 articles.
1. Immunity to uropathogens: the emerging roles of inflammasomes
2. Determinants of quinolone resistance in Escherichia coli causing community-acquired urinary tract infection in Bejaia, Algeria
3. Suppression of gyrase-mediated resistance by C7 aryl fluoroquinolones
4. gyrA Mutations in high-level fluoroquinolone-resistant clinical isolates of Escherichia coli
5. Fluoroquinolone Resistance Among Gram-Negative Urinary Tract Patho-gens: Global Smart Program Results, 2009-2010
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