Please use this identifier to cite or link to this item: http://idr.niser.ac.in:8080/jspui/handle/123456789/1009
Title: Design, Synthesis, and Evaluation of Thiol-Activated Sources of Sulfur Dioxide (SO2) as Antimycobacterial Agents
Authors: Konkimalla, V. Badireenath
Keywords: Amines
Group 16 compounds
Inhibition
Oxides
Thiols
Issue Date: 30-Nov-2011
Publisher: Journal of Medicinal Chemistry
Citation: Malwal, S. R., Sriram, D., Yogeeswari, P., Konkimalla, V. B., & Chakrapani, H. (2012). Design, synthesis, and evaluation of thiol-activated sources of sulfur dioxide (SO₂) as antimycobacterial agents. Journal of Medicinal Chemistry, 55(1), 553–557.
Abstract: Here, 2,4-dinitrophenylsulfonamides with tunable cysteine-activated SO2 release profiles with half-lives of SO2 release varying from 2 to 63 min are reported. N-Benzyl-2,4-dinitrobenzenesulfonamide (6), which is prepared in one step from commercial sources, had a potency (MIC = 0.15 μM) of inhibiting Mycobacterium tuberculosis (Mtb) higher than the clinical agent isoniazid (MIC = 0.37 μM).
URI: https://doi.org/10.1021/jm201023g
http://idr.niser.ac.in:8080/jspui/handle/123456789/1009
Appears in Collections:Journal Papers

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