Novel fluorobenzothiazole as a dual inhibitor of gyrase B and topoisomerase IV against Gram-positive pathogens

Author:

Barman Tarani K12,Kumar Manoj123ORCID,Chaira Tridib456,Singhal Smita12,Mathur Tarun12,Kalia Vandana12,Gangadharan Ramkumar126,Rao Madhvi12,Pandya Manisha12,Bhateja Pragya12,Sood Ruchi12,Upadhyay Dilip J12,Varughese Shibu78,Yadav Ajay78,Sharma Lalima78,Ramadass Venkataramanan78,Kumar Naresh78,Sattigeri Jitendra78,Bhatnagar Pradip K78,Raj V Samuel129

Affiliation:

1. Department of Infectious Diseases, New Drug Discovery Research, Ranbaxy Research Laboratories, R & D III, Sector-18, Gurgaon, 122 015, India

2. Department of Microbiology, Daiichi Sankyo India Pharma Private Limited, Village Sarhaul, Sector-18, Gurgaon, 122 015, India

3. Research Department, Sidra Medicine, Doha, 26999, Qatar

4. Department of Metabolism & Pharmacokinetics, New Drug Discovery Research, Ranbaxy Research Laboratories, R & D III, Sector-18, Gurgaon, 122 015, India

5. Department of Drug Metabolism & Pharmacokinetics, Daiichi Sankyo India Pharma Private Limited, Village Sarhaul, Sector-18, Gurgaon, 122 015, India

6. Department of Pharmacology, SGT University, Gurugram, 122505, Haryana, India

7. Department of Chemistry, New Drug Discovery Research, Ranbaxy Research Laboratories, R & D III, Sector-18, Gurgaon, 122 015, India

8. Department of Chemistry, Daiichi Sankyo India Pharma Private Limited, Village Sarhaul, Sector-18, Gurgaon, 122 015, India

9. Centre for Drug Design Discovery & Development (C4D), SRM University, Delhi-NCR, Sonepat, 131 029, Haryana, India

Abstract

Aim: The development of a novel inhibitor targeting gyrase B and topoisomerase IV offers an opportunity to combat multidrug resistance. Methods: We investigated the activity of RBx 10080758 against Gram-positive bacteria in vitro and in vivo. Results: RBx 10080758 showed a potent 50% inhibitory concentration of 0.13 μM and 0.25 μM against gyrase B and topoisomerase IV, respectively, and exhibited strong whole-cell in vitro activity with MIC ranges of 0.015–0.06 and 0.015–0.03 μg/ml against Staphylococcus aureus and Streptococcus pneumoniae, respectively. In a rat thigh infection model with methicillin-resistant S. aureus, RBx 10080758 at 45 mg/kg exhibited a >3 log10 CFU reduction in thigh muscles. Conclusion: RBx 10080758 displayed potent activity against multiple multidrug-resistant Gram-positive bacteria with a dual-targeting mechanism of action.

Publisher

Future Medicine Ltd

Subject

Microbiology (medical),Microbiology

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