Murthy Boddapati S N, Talari Subrahmanyam, Kola A Emmanuel, Chalapaka Bhuvaneswari
Department of Chemistry, Sir C R Reddy Autonomous College, Eluru, India.
Turk J Chem. 2022 Jan 13;46(3):766-776. doi: 10.55730/1300-0527.3366. eCollection 2022.
Ten novel 2-aryl-5-(arylsulfonyl)-1,3,4-oxadiazoles were produced and assessed for their antibacterial and antioxidant activities. Diverse spectroscopic methods like H NMR, C NMR, IR, and LCMS were used for the characterization of the prepared samples and all the data was in good agreement with the anticipated structures. The prepared compounds were screened for their in vitro antibacterial activity against bacterial strains , , (gram-positive), and , , (gram-negative). The antimicrobial screening outcome revealed that the prepared 2-(3,4-dimethylphenyl)-5-tosyl-1,3,4-oxadiazole (), 2-(3-isopropylphenyl)-5-tosyl-1,3,4-oxadiazole (), and 2-(2-ethylphenyl)-5-tosyl-1,3,4-oxadiazole () are most potent among all the examined compounds. Furthermore, the antioxidant activity of the prepared compounds was also investigated by DPPH radical scavenging method and the results showed that some of the compounds were moderately active.
制备了十种新型的2-芳基-5-(芳基磺酰基)-1,3,4-恶二唑,并对其抗菌和抗氧化活性进行了评估。使用了多种光谱方法,如¹H NMR、¹³C NMR、IR和LCMS对制备的样品进行表征,所有数据与预期结构吻合良好。对制备的化合物针对细菌菌株枯草芽孢杆菌、金黄色葡萄球菌、表皮葡萄球菌(革兰氏阳性菌)以及大肠杆菌、铜绿假单胞菌、肺炎克雷伯菌(革兰氏阴性菌)进行了体外抗菌活性筛选。抗菌筛选结果表明,制备的2-(3,4-二甲基苯基)-5-对甲苯磺酰基-1,3,4-恶二唑(化合物4)、2-(3-异丙基苯基)-5-对甲苯磺酰基-1,3,4-恶二唑(化合物5)和2-(2-乙基苯基)-5-对甲苯磺酰基-1,3,4-恶二唑(化合物6)在所有检测化合物中活性最强。此外,还通过DPPH自由基清除法研究了制备化合物的抗氧化活性,结果表明其中一些化合物具有中等活性。