| Literature DB >> 27503657 |
Boris V Nikonenko1, Albert Kornienko2, Konstantin Majorov3, Pavel Ivanov2, Tatiana Kondratieva3, Maria Korotetskaya3, Alexander S Apt4, Elena Salina5, Valeriya Velezheva6.
Abstract
Among 230 target-synthesized indole-based compounds, seven 3-triazenoindoles showed MICs of 0.2 to 0.5 μg/ml against Mycobacterium tuberculosis strain H37Rv and isoniazid-resistant human isolate CN-40. The TU112 compound was active also against a dormant form of M. tuberculosis Some of these triazenoindoles were active against Mycobacterium avium, with MICs of 0.05 to 0.5 μg/ml. The selectivity indices (SI) for M. tuberculosis and M. avium were significantly higher than 10, making these compounds acceptable for the next testing step.Entities:
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Year: 2016 PMID: 27503657 PMCID: PMC5038256 DOI: 10.1128/AAC.00998-16
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191