Article ID Journal Published Year Pages File Type
10588000 Bioorganic & Medicinal Chemistry Letters 2013 4 Pages PDF
Abstract
The readily available 3H-1,2,4-dithiazol-3-one molecule compound 4n was shown to be potent against the virulent Mycobacterium tuberculosis H37Rv strain by a microdilution method, demonstrating a better safety profile on human normal liver L02 cells than the lead compound HT1171, which was reported as a potent proteasome inhibitor of Mycobacterium bovis var. bacilli Calmette-Guérin (BCG).
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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