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
  • 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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