Methyl sulfonamide substituents improve the pharmacokinetic properties of bicyclic 2-pyridone basedChlamydia trachomatisinhibitors

Author:

Kulén Martina12345,Núñez-Otero Carlos52346ORCID,Cairns Andrew G.12345,Silver Jim52347,Lindgren Anders E. G.12345,Wede Emma52347,Singh Pardeep12345,Vielfort Katarina52347,Bahnan Wael52347,Good James A. D.12345,Svensson Richard8910114,Bergström Sven52347,Gylfe Åsa52346,Almqvist Fredrik12345

Affiliation:

1. Department of Chemistry

2. Umeå University

3. 901 87 Umeå

4. Sweden

5. Umeå Centre for Microbial Research

6. Laboratory for Molecular Infection Medicine Sweden (MIMS)

7. Department of Molecular Biology

8. The Uppsala University Drug Optimization and Pharmaceutical Profiling Platform

9. Department of Pharmacy

10. Uppsala University

11. SE-751 23 Uppsala

Abstract

Methyl sulfonamide substituents effectively improve the pharmacokinetic properties of bicyclic 2-pyridones, a new class ofChlamydia trachomatisinfectivity inhibitors.

Funder

Vetenskapsrådet

Knut and Alice Wallenberg Foundation

Kempestiftelserna

Stiftelsen för Strategisk Forskning

Göran Gustafssons Stiftelse för Naturvetenskaplig och Medicinsk Forskning

Publisher

Royal Society of Chemistry (RSC)

Subject

Pharmaceutical Science,Biochemistry,Drug Discovery,Molecular Medicine,Pharmacology,Organic Chemistry

Reference24 articles.

1. World Health Organization , Global incidence and prevalence of selected curable sexually transmitted infections – 2008, 978 92 4 150383 9, World Health Organization , Geneva, Switzerland , 2012

2. Human chlamydial infections: persistence, prevalence, and outlook for the future

3. Chlamydial metabolism revisited: interspecies metabolic variability and developmental stage-specific physiologic activities

4. Mechanisms of host cell exit by the intracellular bacterium Chlamydia

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