1. Academic Validation
  2. Diphenylether-Modified 1,2-Diamines with Improved Drug Properties for Development against Mycobacterium tuberculosis

Diphenylether-Modified 1,2-Diamines with Improved Drug Properties for Development against Mycobacterium tuberculosis

  • ACS Infect Dis. 2016 Jul 8;2(7):500-8. doi: 10.1021/acsinfecdis.6b00052.
Marie H Foss 1 Sovitj Pou 2 Patrick M Davidson 1 Jennifer L Dunaj 1 Rolf W Winter 2 Sovijja Pou 2 Meredith H Licon 1 Julia K Doh 1 Yuexin Li 2 Jane X Kelly 2 Rozalia A Dodean 2 Dennis R Koop 3 Michael K Riscoe 1 2 Georgiana E Purdy 1
Affiliations

Affiliations

  • 1 Department of Molecular Microbiology & Immunology, Oregon Health & Science University , 3181 S.W. Sam Jackson Park Road, Portland, Oregon 97239, United States.
  • 2 Portland VA Medical Center , 3710 S.W. U.S. Veterans Hospital Road, Portland, Oregon 97239, United States.
  • 3 Department of Physiology and Pharmacology, Oregon Health & Science University , 3181 S.W. Sam Jackson Park Road, Portland, Oregon 97239, United States.
Abstract

New treatments for tuberculosis Infection are critical to combat the emergence of multidrug- and extensively drug-resistant Mycobacterium tuberculosis (Mtb). We report the characterization of a diphenylether-modified adamantyl 1,2-diamine that we refer to as TBL-140, which has a minimal inhibitory concentration (MIC99) of 1.2 μg/mL. TBL-140 is effective against drug-resistant Mtb and nonreplicating bacteria. In addition, TBL-140 eliminates expansion of Mtb in Cell Culture infection assays at its MIC. To define the mechanism of action of this compound, we performed a spontaneous mutant screen and biochemical assays. We determined that TBL-140 treatment affects the proton motive force (PMF) by perturbing the transmembrane potential (ΔΨ), consistent with a target in the electron transport chain (ETC). As a result, treated bacteria have reduced intracellular ATP levels. We show that TBL-140 exhibits greater metabolic stability than SQ109, a structurally similar compound in clinical trials for treatment of MDR-TB infections. Combined, these results suggest that TBL-140 should be investigated further to assess its potential as an improved therapeutic lead against Mtb.

Keywords

MmpL3; antibiotic; drug development; proton motive force; tuberculosis.

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