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首页> 外文期刊>Molecules >Synthesis of Novel Symmetrical 1,4-Disubstituted 1,2,3-Bistriazole Derivatives via 'Click Chemistry' and Their Biological Evaluation
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Synthesis of Novel Symmetrical 1,4-Disubstituted 1,2,3-Bistriazole Derivatives via 'Click Chemistry' and Their Biological Evaluation

机译:通过“点击化学”合成新型对称的1,4-二取代的1,2,3-双三唑对称衍生物及其生物学评价

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摘要

A series of symmetric bis-1,2,3-triazole compounds 2-5(a-f) were synthesized as potential antioxidant agents via click chemistry. Their structures were confirmed by H-1-NMR and C-13-NMR. All of the synthesized compounds were subjected to antioxidant and antimicrobial assays. The antioxidant activity of these compounds (AChE inhibition, DPPH and SOD activities) was evaluated. Compound 2f was found to show the highest AChE inhibition activity of all compounds, while compound 3b showed a strong inhibitory effect on DPPH radical and compound 2a was the most effective of all compounds for SOD activity. All synthesized compounds were found to possess moderate antibacterial activity against the bacteria E. coli and Y. pseudotuberculosis.
机译:通过点击化学合成了一系列对称的双1,2,3-三唑化合物2-5(a-f)作为潜在的抗氧化剂。其结构通过H-1-NMR和C-13-NMR确认。对所有合成的化合物进行抗氧化剂和抗菌测定。评估了这些化合物的抗氧化活性(抑制AChE,DPPH和SOD活性)。发现化合物2f在所有化合物中均显示出最高的AChE抑制活性,而化合物3b对DPPH自由基显示出较强的抑制作用,而化合物2a在所有化合物中对SOD活性最有效。发现所有合成的化合物对细菌大肠杆菌和假结核耶尔森氏菌均具有中等的抗菌活性。

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