
ABSTRACT Translocase I inhibitor compounds derived from capuramycin demonstrated rapid bactericidal activity against several different mycobacterial species. SQ641 was the most active of the compounds, with a MIC of 0.12 to 8 μg/ml, a postantibiotic effect of 55 h, and interesting synergistic effects with other antitubercular drugs.
Aminoglycosides, Antitubercular Agents, Humans, Nucleosides, Microbial Sensitivity Tests, Mycobacterium tuberculosis, Mycobacterium avium Complex, Mycobacterium
Aminoglycosides, Antitubercular Agents, Humans, Nucleosides, Microbial Sensitivity Tests, Mycobacterium tuberculosis, Mycobacterium avium Complex, Mycobacterium
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