Please use this identifier to cite or link to this item: http://localhost:80/xmlui/handle/123456789/14760
Title: Synthesis, Bacterial biofilm inhibition and cytotoxicity of new NAlkyl/aralkyl-N-(2,3-dihydro-1,4-benzodioxin-6-yl)-4- nitrobenzenesulfonamides
Authors: Abbasi, Muhammad Athar
Zeb, Aurang
Rehman, Aziz-ur
Siddiqui, Sabahat Zahra
Ali Shah, Syed Adnan
Shahid, Muhammad
Fatima, Hina
Keywords: N-(2,3-Dihydro-1,4-benzodioxin-6-yl)-4-nitrobenzenesulfonamide
alkyl/ aralkyl halides
spectral analysis
biofilm inhibition
antibacterial
cytotoxicity
Issue Date: 6-Jan-2020
Publisher: Karachi: Faculty of Pharmacy & Pharmaceutical Sciences, Karachi
Citation: Abbasi, M. A., Zeb, A., Siddiqui, S. Z., Shah, S. A. A., Shahid, M., & Fatima, H. (2020). Synthesis, Bacterial biofilm inhibition and cytotoxicity of new N-Alkyl/aralkyl-N-(2, 3-dihydro-l, 4-benzodioxin-6-yl)-4-nitrobenzenesulfonamides. Pakistan journal of pharmaceutical sciences, 33(1), 41-48.
Abstract: The current research was commenced by reaction of 1,4-benzodioxane-6-amine (1) with 4- nitrobenzenesulfonyl chloride (2) in the presence of aqueous base under dynamic pH control at 9 to yield N-(2,3-dihydro1,4-benzodioxin-6-yl)-4-nitrobenzenesulfonamide (3) which was further reacted with a series of alkyl/aralkyl halides (4a-i) in polar aprotic solvent using catalytic amount of lithium hydride which acts as base to afford some new Nalkyl/aralkyl-N-(2,3-dihydro-1,4-benzodioxin-6-yl)-4-nitrobenzenesulfonamides (5a-i). The projected structures of all the synthesized derivatives were characterized by contemporary techniques i.e., IR, 1H-NMR and EIMS. The biofilm Inhibitory action of all synthesized molecules was carried out against Escherichia coli and Bacillus subtilis. It was inferred from their results that 5f and 5e exhibited suitable inhibitory action against the biofilms of these bacterial strains. Moreover, their cytotoxicity was also checked and it was concluded that these synthesized molecules displayed docile cytotoxicity.
URI: http://142.54.178.187:9060/xmlui/handle/123456789/14760
ISSN: 1011-601X
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