Synthesis and biological Evaluation of some new Amide Derivatives of Sulphonamide

H. Pal, Arvind Kumar, Sonu, B. Parveen, S. Praveen
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引用次数: 2

Abstract

A series of substituted amide derivatives of Sulphonamides were synthesized, and their anticonvulsant activity and antimicrobial activity were evaluated which include the MES model and by Cup-plate method. However, further studies need to be carried out to ascertain the precise mechanism of action of anticonvulsant activity of these molecules. The compounds.N-(4-Acetylsulfamoyl-phenyl)-4-(4-chloro-3-methyl-phenyl)-4-oxo-butyramide (HP-1) showed significant anticonvulsant activity. Some compounds show the good antibacterial activity against Escherichia coli. The Compound 4-(4-chloro-3-methyl-phenyl)-4-oxo-N-(4-sulfamoyl-phenyl)-butyramide (HP-2) and 4-(4-Methoxy-phenyl)-4-oxo-N-(4-Sulfomoyl-Phenyl-)butyramide(HP-3) showed significant inhibitory characteristics with stronger antimicrobial activity against MTCC-521 gram(-)ve bacteria.
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磺胺类新酰胺类衍生物的合成及生物学评价
合成了一系列磺胺类取代酰胺衍生物,并采用MES模型和杯盘法对其抗惊厥活性和抗菌活性进行了评价。然而,需要进一步的研究来确定这些分子抗惊厥活性的确切作用机制。化合物n -(4-乙酰氨基甲酰苯基)-4-(4-氯-3-甲基苯基)-4-氧-丁酰胺(HP-1)具有显著的抗惊厥活性。部分化合物对大肠杆菌具有良好的抑菌活性。化合物4-(4-氯-3-甲基苯基)-4-氧- n -(4-磺酰基苯基)-丁酰胺(HP-2)和4-(4-甲氧基苯基)-4-氧- n -(4-磺酰基苯基)丁酰胺(HP-3)对MTCC-521 g (-)ve细菌具有较强的抑菌活性。
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