Lamut, Andraž and Skok, Žiga and Barančoková, Michaela and Gutierrez, Lucas J. and Cruz, Cristina D. and Draskovits, Gábor and Szili, Petra Éva and Nyerges, Ákos and Pál, Csaba (2020) Second generation 4,5,6,7-tetrahydrobenzo[d]thiazoles as novel DNA gyrase inhibitors. FUTURE MEDICINAL CHEMISTRY, 12 (4). pp. 277-297. ISSN 1756-8919 (print); 1756-8927 (online)
![]() |
Text
LamutFutureMedChem.pdf Restricted to Registered users only Download (1MB) |
Abstract
Aim: 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. Results: Building from our first generation of 4,5,6,7-tetrahydrobenzo[d]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 Staphylococcus aureus and Escherichia coli, with IC50 values in the nanomolar range. Importantly, these inhibitors also show improved antibacterial activity against Gram-positive strains. Conclusion: The most promising inhibitor, 29, is active against Enterococcus faecalis, Enterococcus faecium and S. aureus 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.
Item Type: | Article |
---|---|
Uncontrolled Keywords: | antibacterial; DNA gyrase; inhibitor; pyrrolamide; QTAIM; thiazole |
Subjects: | Q Science / természettudomány > QH Natural history / természetrajz > QH426 Genetics / genetika, örökléstan |
SWORD Depositor: | MTMT SWORD |
Depositing User: | MTMT SWORD |
Date Deposited: | 22 Jan 2021 10:37 |
Last Modified: | 22 Jan 2021 10:37 |
URI: | http://real.mtak.hu/id/eprint/119878 |
Actions (login required)
![]() |
Edit Item |