Baseer Muhammad, Ansari Farzana Latif, Ashraf Zaman
Chemistry Department, Quaid-i-azam University, Islamabad, Pakistan.
Pak J Pharm Sci. 2013 Jan;26(1):67-73.
Fourteen new N-acetylated and non-acetylated pyrazoline derivatives were synthesized by reacting chalcones with hydrazine in the presence of absolute ethanol however reaction was carried out in the presence of glacial acetic acid to afford N-acetylated pyrazolines. The chemical structures of the synthesized pyrazolines were confirmed by FTIR, (1)HNMR, (13)CNMR and mass spectroscopic data. The pyrazolines (1-14) were screened for antibacterial activity against ten bacterial strains using seven Gram-positive and three Gram-negative bacteria and antifungal activity against Aspergillus flavus, Aspergillus niger and Aspergillus pterus. Pyrazolines (1-14) found to exhibit good to excellent antimicrobial activities compared to the levofloxacin and fluconazole used as standard drugs.
通过在无水乙醇存在下使查尔酮与肼反应合成了十四种新的N-乙酰化和非乙酰化吡唑啉衍生物,不过反应是在冰醋酸存在下进行的,以得到N-乙酰化吡唑啉。通过傅里叶变换红外光谱(FTIR)、核磁共振氢谱(¹HNMR)、核磁共振碳谱(¹³CNMR)和质谱数据确定了合成的吡唑啉的化学结构。使用七种革兰氏阳性菌和三种革兰氏阴性菌对吡唑啉(1-14)针对十种细菌菌株的抗菌活性以及对黄曲霉、黑曲霉和翼状曲霉的抗真菌活性进行了筛选。与用作标准药物的左氧氟沙星和氟康唑相比,吡唑啉(1-14)表现出良好到优异的抗菌活性。