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Published on: August 22, 2018
Enantiopure antituberculosis candidates synthesized from (-)-fenchone
Georgi M Dobrikov1, Violeta Valcheva2, Yana Nikolova1
1Institute of Organic Chemistry with Centre of Phytochemistry, Bulgarian Academy of Sciences, Bl. 9, Acad. G. Bonchev Str., Sofia 1113, Bulgaria.
Abstract:
The synthesis of new enantiopure N-acyl compounds derived from (-)-fenchone has been performed. The evaluation of their in vitro activity against Mycobacterium tuberculosis H37Rv showed for most of them moderate activity. The structures bearing sulfonamide functionality have comparable activity to ethambutol and possess low cytotoxicity.
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