Synthesis and urease inhibitory potential of benzophenone sulfonamide hybrid in vitro and in silico
作者:Arshia、Farida Begum、Noor Barak Almandil、Muhammad Arif Lodhi、Khalid Mohammed Khan、Abdul Hameed、Shahnaz Perveen
DOI:10.1016/j.bmc.2019.01.043
日期:2019.3
This study deals with the synthesis of benzophenone sulfonamides hybrids (1-31) and screening against urease enzyme in vitro. Studies showed that several synthetic compounds were found to have good urease enzyme inhibitory activity. Compounds 1 (N'-((4'-hydroxyphenyl)(phenyl)methylene)-4 ''-nitrobenzenesulfonohy-drazide), 2 (N'-((4'-hydroxyphenyl)(phenyl)methylene)-3 ''-nitrobenzenesulfonohydrazide), 3 (N'-((4'-hydroxyphenyl)(phenyl)methylene)-4 ''-methoxybenzenesulfonohydrazide), 4 (3 '',5 ''-dichloro-2 ''-hydroxy-N'-((4'-hydroxyphenyl)(phenyl)methylene)benzenesulfonohydrazide), 6 (2 '',4 ''-dichloro-N'-((4'-hydroxyphenyl)(phenyl)methylene)benzenesulfonohydrazide), 8 (5-(dimethylamino)-N'-((4-hydroxyphenyl)(phenyel)methylene)naphthalene-1-sulfono hydrazide), 10 (2 ''-chloro-N'-((4'-hydroxyphenyl)(phenyl)methylene)benzenesulfonohydrazide), 12 (N'-((4'-hydroxyphenyl)(phenyl)methylene)benzenesulfonohydrazide) have found to be potently active having an IC50, value in the range of 3.90-17.99 mu M. These compounds showed superior activity than standard acetohydroxamic acid (IC50 = 29.20 +/- 1.01 mu M). Moreover, in silico studies on most active compounds were also performed to understand the binding interaction of most active compounds with active sites of urease enzyme. Structures of all the synthetic compounds were elucidated by H-1 NMR, C-13 NMR, EI-MS and FAB-MS spectroscopic techniques.
Copper-Catalyzed Nitrogen Loss of Sulfonylhydrazones: A Reductive Strategy for the Synthesis of Sulfones from Carbonyl Compounds
An efficient method for the synthesis of sulfones via nitrogen loss of sulfonyl hydrazones is described. The reaction was performed in the presence of simple copper salt and base by utilization of sulfonyl hydrazones, which were easily prepared from carbonyl compounds. A wide variety of aryl and alkyl sulfones were obtained in moderate to good yields.