An antimycobacterial pleuromutilin analogue effective against dormant bacilli

  • Bioorg Med Chem. 2018 Sep 15;26(17):4787-4796. doi: 10.1016/j.bmc.2018.07.034.
Maddie R Lemieux  1 ,  Shajila Siricilla  1 ,  Katsuhiko Mitachi  1 ,  Shakiba Eslamimehr  1 ,  Yuehong Wang  2 ,  Dong Yang  3 ,  Jeffrey D Pressly  1 ,  Ying Kong  3 ,  Frank Park  1 ,  Scott G Franzblau  2 ,  Michio Kurosu  4
Affiliations
  • 1. Department of Pharmaceutical Sciences, College of Pharmacy, University of Tennessee Health Science Center, 881 Madison Avenue, Memphis, TN 38163-0001, United States.
  • 2. Institute for Tuberculosis Research, College of Pharmacy, University of Illinois at Chicago, 833 S. Wood Street, Chicago, IL 60612, United States.
  • 3. Department of Microbiology, Immunology & Biochemistry, University of Tennessee Health Science Center, 858 Madison Avenue, Memphis, TN 38163-0001, United States.
  • 4. Department of Pharmaceutical Sciences, College of Pharmacy, University of Tennessee Health Science Center, 881 Madison Avenue, Memphis, TN 38163-0001, United States. Electronic address: [email protected].
Abstract

Pleuromutilin is a promising pharmacophore to design new Antibacterial agents for Gram-positive bacteria. However, there are limited studies on the development of pleuromutilin analogues that inhibit growth of Mycobacterium Tuberculosis (Mtb). In screening of our library of pleuromutilin derivatives, UT-800 (1) was identified to kill replicating- and non-replicating Mtb with the MIC values of 0.83 and 1.20 μg/mL, respectively. UT-800 also kills intracellular Mtb faster than rifampicin at 2× MIC concentrations. Pharmacokinetic studies indicate that 1 has an oral bioavailability with an average F-value of 27.6%. Pleuromutilin may have the potential to be developed into an orally administered anti-TB drug.

Keywords
Antimycobacterial activity; Dormant tuberculosis; Intracellular Mycobacterium tuberculosis; Pharmacokinetics; Pleuromutilin.