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-  2018 

N-[2-(1H-Indol-3-yl)-1-(5-thioxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)ethyl]-4-methylbenzenesulfonamide

DOI: https://doi.org/10.3390/M1008

Keywords: oxadiazole, molecular docking, enoyl reductase (InhA)

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Abstract:

Abstract N-[1-Hydrazinyl-3-(1 H-indol-3-yl)-1-oxopropan-2-yl]-4-methylbenzenesulfonamide ( 1) on cyclization with carbon disulfide in ethanolic potassium hydroxide affords N-[2-(1 H-indol-3-yl)-1-(5-thioxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)ethyl]-4-methylbenzenesulfonamide ( 2) in 84% yield. The structure of compound 2 was supported by mass spectrometry, FT-IR and 1H- and 13C-NMR spectroscopy. To investigate the potential of compound 2 to act as antitubercular agent, it was docked against the enoyl reductase (InhA) enzyme of Mycobacterium tuberculosis. The docking pose and non-covalent interactions gave insights on its plausible inhibitory action. View Full-Tex

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