Reddy P Muralidhar, Ho Yen-Peng, Shanker Kanne, Rohini Rondla, Ravinder Vadde
Department of Chemistry, National Dong Hwa University, Hualien, Taiwan.
Eur J Med Chem. 2009 Jun;44(6):2621-5. doi: 10.1016/j.ejmech.2008.09.035. Epub 2008 Oct 7.
A series of novel macrocyclic compounds were synthesized by the condensation of o-phthalaldehyde with aromatic amino alcohols followed by treatment with 1,2-dibromoethane or 1,3-dibromopropane in non-template method. The structural features of the isolated macrocycles have been determined from the microanalytical, IR, (1)H, (13)C NMR and mass spectral studies. Antimicrobial activities of these macrocyclic compounds were tested against the gram-positive (Bacillus subtilis, Staphylococcus aureus) and gram-negative (Escherichia coli, Klebsiella pneumoniae) bacteria and found to exhibit potential antibacterial activity. The macrocycles were also tested in vitro to evaluate their activity against fungi, namely, Aspergillus flavus (A. flavus) and Fusarium species.
通过邻苯二甲醛与芳香族氨基醇缩合,然后在非模板法中用1,2 - 二溴乙烷或1,3 - 二溴丙烷处理,合成了一系列新型大环化合物。通过微量分析、红外光谱、(1)H、(13)C核磁共振和质谱研究确定了分离出的大环化合物的结构特征。测试了这些大环化合物对革兰氏阳性菌(枯草芽孢杆菌、金黄色葡萄球菌)和革兰氏阴性菌(大肠杆菌、肺炎克雷伯菌)的抗菌活性,发现它们具有潜在的抗菌活性。还对这些大环化合物进行了体外测试,以评估它们对真菌的活性,即黄曲霉和镰刀菌属。