| Literature DB >> 30145051 |
Maddie R Lemieux1, Shajila Siricilla1, Katsuhiko Mitachi1, Shakiba Eslamimehr1, Yuehong Wang2, Dong Yang3, Jeffrey D Pressly1, Ying Kong3, Frank Park1, Scott G Franzblau2, Michio Kurosu4.
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.Entities:
Keywords: Antimycobacterial activity; Dormant tuberculosis; Intracellular Mycobacterium tuberculosis; Pharmacokinetics; Pleuromutilin
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Year: 2018 PMID: 30145051 PMCID: PMC6154393 DOI: 10.1016/j.bmc.2018.07.034
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641