Second generation 4,5,6,7-tetrahydrobenzo[]thiazoles as novel DNA gyrase inhibitors.

Clicks: 350
ID: 94780
2020
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Abstract
DNA gyrase and topoisomerase IV are essential bacterial enzymes, and in the fight against bacterial resistance, they are important targets for the development of novel antibacterial drugs. Building from our first generation of 4,5,6,7-tetrahydrobenzo[]thiazole-based DNA gyrase inhibitors, we designed and prepared an optimized series of analogs that show improved inhibition of DNA gyrase and topoisomerase IV from and , with IC values in the nanomolar range. Importantly, these inhibitors also show improved antibacterial activity against Gram-positive strains. The most promising inhibitor, , is active against , and wild-type and resistant strains, with minimum inhibitory concentrations between 4 and 8 μg/ml, which represents good starting point for development of novel antibacterials.
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lamut2020secondfuture Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Lamut, Andraž;Skok, Žiga;Barančoková, Michaela;Gutierrez, Lucas J;Cruz, Cristina D;Tammela, Päivi;Draskovits, Gábor;Szili, Petra Éva;Nyerges, Ákos;Pál, Csaba;Molek, Peter;Bratkovič, Tomaž;Ilaš, Janez;Zidar, Nace;Zega, Anamarija;Enriz, Ricardo D;Kikelj, Danijel;Tomašič, Tihomir;
Journal Future medicinal chemistry
Year 2020
DOI
10.4155/fmc-2019-0127
URL
Keywords
antibacterial inhibitor thiazole dna gyrase qtaim pyrrolamide

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