The riminophenazine agent clofazimine (CFZ) is repurposed as an important component of the new short-course multidrug-resistant tuberculosis regimen and significantly shortens first-line regimen for drug-susceptible tuberculosis in mice. However, CFZ use is hampered by its unwelcome skin discoloration in patients. A new riminophenazine analog, TBI-166, was selected as a potential next-generation antituberculosis riminophenazine following an extensive medicinal chemistry effort. Here, we evaluated the activity of TBI-166 against and its potential to accumulate and discolor skin. The activity of TBI-166 against both drug-sensitive and drug-resistant is more potent than that of CFZ. Spontaneous mutants resistant to TBI-166 were found at a frequency of 2.3 × 10 in wild strains of TBI-166 demonstrates activity at least equivalent to that of CFZ against intracellular and in low-dose aerosol infection models of acute and chronic murine tuberculosis. Most importantly, TBI-166 causes less skin discoloration than does CFZ despite its higher tissue accumulation. The efficacy of TBI-166, along with its decreased skin pigmentation, warrants further study and potential clinical use.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6496038 | PMC |
http://dx.doi.org/10.1128/AAC.02155-18 | DOI Listing |
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