首页> 外文期刊>Beni-Suef University Journal of Basic and Applied Sciences >Synthesis and spectroscopic characterisation of novel bioactive molecule of 3-(2-substituted)-1H-indol-3-yl)-1-(thiophen-2yl)prop-2-en-1-one chalcone derivatives as effective anti-oxidant and anti-microbial agents
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Synthesis and spectroscopic characterisation of novel bioactive molecule of 3-(2-substituted)-1H-indol-3-yl)-1-(thiophen-2yl)prop-2-en-1-one chalcone derivatives as effective anti-oxidant and anti-microbial agents

机译:3-(2-取代)-1H-吲哚-3-基)-1-(噻吩-2基)丙-2-烯-1-酮查尔酮衍生物作为有效抗氧化剂的新型生物活性分子的合成及光谱表征抗菌剂

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The chief purpose of this work was to synthesise and find out the anti-oxidant and anti-microbial activities of novel 3-(2-substituted)-1H-indol-3-yl)-1-(thiophen-2yl)prop-2-en-1-one chalcone derivatives. These derivatives were prepared by performing Claisen–Schmidt condensation reaction of 1-(thiophen-2yl)ethanone and 2 substituted 1H-indole-3-carbaldehyde with constant stirring (approximately for 3 hours) in the presence of ethanol and potassium hydroxide. The newly synthesised compounds' anti-oxidant and anti-microbial activities have been identified by using DPPH radical scavenging assay, zone of inhibition and minimum inhibitory concentration. Most of the prepared compounds had shown excellent anti-oxidant and anti-microbial activities as compared to the standard drugs like Ascorbic acid, Ciprofloxacin and Fluconazole. Among the synthesised compounds, compounds 4e, 4h and 4a showed remarkable activity at low concentration. Therefore, these compounds deserve further research.
机译:这项工作的主要目的是合成并发现新型3-(2-取代)-1H-吲哚-3-基)-1-(噻吩-2基)prop-2的抗氧化和抗菌活性。 -en-1-一个查尔酮衍生物。这些衍生物是在乙醇和氢氧化钾存在下,在持续搅拌(约3小时)的条件下,进行1-(噻吩-2-基)乙酮与2个取代的1H-吲哚-3-甲醛的Claisen-Schmidt缩合反应而制备的。通过DPPH自由基清除法,抑菌圈和最小抑菌浓度鉴定了新合成的化合物的抗氧化和抗菌活性。与标准药物(如抗坏血酸,环丙沙星和氟康唑)相比,大多数制备的化合物均具有出色的抗氧化和抗微生物活性。在合成的化合物中,化合物4e,4h和4a在低浓度下显示出显着的活性。因此,这些化合物值得进一步研究。

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