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首页> 外文期刊>Research journal of pharmacy and technology >Synthesis and Antimicrobial Activity of Some Sulfonamide Derivatives containing various Heterocyclic Moieties
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Synthesis and Antimicrobial Activity of Some Sulfonamide Derivatives containing various Heterocyclic Moieties

机译:含有各种杂环部分的一些磺酰胺衍生物的合成和抗微生物活性

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摘要

A series of new sulfonamide derivatives derived from N-(4-acetylphenyl)-4-methylbenzenesulfonamide bearing different heterocyclic moieties such as 1,3-thiazole, 2-azetidinone and 4- thiazolidinone. The newly synthesized sulfhamide derivatives have been characterized by FTIR, 1H NMR, Mass spectra and elemental analysis. All the synthesized compounds were screened for their antimicrobial activity and compared with reference drug Amoxicillin. Heterocycleshave attracted thepresence of sulphonamide fragments in the attention of chemists because of their important biological properties and their role as pharmacofores [1-5]. Thiazole ring system has been consistently rewarded as alpromising molecule because of its broad spectrum of pharmaceutical activities like antimicrobial and anticancer [6-8]. Furthermore,derivaties containingSchifF base (azomethine) are a species of important compounds in medical chemistry and pharmacological field [9,10]. 2-Azetidinone have been found to be an important moiety in creation of novel medical drugs and they encompass pharmacological activities [11-14]. On the other hand, the 4-thiazolidinone scaffold is very versatile and has featured in a number of medicinal chemistry. They have found uses as antitubercular, antimicrobial and anticancer [13-15]. Tetrazole and their derivatives are found in many of the bioactive heterocyclic compounds that are of great interest due to various biological, and clinical applications [16,17].
机译:一系列新的磺酰胺衍生物衍生自N-(4-乙酰基苯基)-4-甲基苯磺酰胺含有不同的杂环部分,例如1,3-噻唑,2-氮杂萘酮和4-噻唑烷酮。新合成的磺胺胺衍生物的特征在于FTIR,1H NMR,质谱和元素分析。将所有合成的化合物筛选其抗微生物活性并与参考药物阿莫西林相比。由于其重要的生物学性质及其作为药物的作用,杂阳性杂交在化学家的注意力中引起了化学家的注意力[1-5]。由于其抗微生物和抗癌等广泛的药物活性,噻唑环系统一直奖励为醛固分子[6-8]。此外,衍生物含有Chockiff碱(Azomethine)是医学化学和药理学田中的重要化合物[9,10]。已发现2-氮杂萘醌是创造新型医用药物的重要部分,它们包括药理学活动[11-14]。另一方面,4-噻唑烷酮支架是非常通用的,并且在许多药用化学中具有特征。他们发现用途用作抗细胞,抗菌剂和抗癌者[13-15]。在许多生物活性杂环化合物中发现四唑及其衍生物由于各种生物学和临床应用而具有巨大兴趣的生物活性杂环化合物[16,17]。

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