Piperidine-4-Carboxamides Target DNA Gyrase in Mycobacterium abscessus

Author:

Negatu Dereje Abate12,Beuchel Andreas3,Madani Abdeldjalil1,Alvarez Nadine1,Chen Chao1,Aragaw Wassihun Wedajo1,Zimmerman Matthew D.1,Laleu Benoît4,Gengenbacher Martin15ORCID,Dartois Véronique15ORCID,Imming Peter3,Dick Thomas156ORCID

Affiliation:

1. Center for Discovery and Innovation, Hackensack Meridian Health, Nutley, New Jersey, USA

2. Center for Innovative Drug Development and Therapeutic Trials for Africa (CDT-Africa), Addis Ababa University, Addis Ababa, Ethiopia

3. Institut für Pharmazie, Martin-Luther-Universität Halle-Wittenberg, Halle, Germany

4. Medicines for Malaria Venture, Geneva, Switzerland

5. Department of Medical Sciences, Hackensack Meridian School of Medicine, Nutley, New Jersey, USA

6. Department of Microbiology and Immunology, Georgetown University, Washington, DC, USA

Abstract

New, more-effective drugs for the treatment of lung disease caused by nontuberculous mycobacteria (NTM) are needed. Among NTM opportunistic pathogens, Mycobacterium abscessus is the most difficult to cure and intrinsically multidrug resistant. In a whole-cell screen of a compound collection active against Mycobacterium tuberculosis , we previously identified the piperidine-4-carboxamide (P4C) MMV688844 (844) as a hit against M. abscessus .

Funder

HHS | National Institutes of Health

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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