作者:Muhammad Iqbal、Rubina Iqbal、Muhammad Bilal、Muhammad Akram、Imam Bakhsh Baloch、Musa Kaleem Baloch
DOI:10.14233/ajchem.2014.16959
日期:——
Present study describes the antimicrobial activities of the di- and tri-substituted benzyl monoesters (1-27) derived from succinic anhydride. The monoesters were screened against two fungi (C. albicans and A. niger) and two bacteria (E. coli, P. mirabilis) strains. All the compounds displayed bioactivity against screened microbes. However, the activities were dependent on the nature of the substituents. Zones of inhibition and minimum inhibitory concentrations (MICs) of the monoesters are reported. Chloramphenicol and ketoconazole were used as standard antibacterial and antifungal drugs respectively.
本研究描述了由琥珀酸酐衍生的二取代和三取代苄基单酯(1-27)的抗微生物活性。对两种真菌(白色念珠菌和黑曲霉)以及两种细菌(大肠杆菌和变形杆菌)进行了筛选。所有化合物对筛选出的微生物均展示了生物活性。然而,这些活性依赖于取代基的性质。报告了单酯的抑制圈和最低抑菌浓度(MIC)。氯霉素和酮康唑分别用于对照抗菌和抗真菌药物。