Nowakowska Z, Wyrzykiewicz E, Kedzia B
Faculty of Chemistry, Adam Mickiewicz University, Poznań, Poland.
Farmaco. 2001 Apr;56(4):325-9. doi: 10.1016/s0014-827x(01)01072-2.
Syntheses of 11 new N-bromoalkyl substituted bromides of (E)-4-azachalcone and N-o-(m- and p-) halobenzyl substituted halides of (E)-3'-hydroxy-4-azachalcone of antimicrobial activity are reported. Compounds 3d, 3e, 6b, 6c, and 6e reveal good antimicrobial activity against Staphylococcus aureus and Enterococcus faecalis as well as moderate activity against Escherichia coli and Klebsiella pneumoniae.
报道了11种具有抗菌活性的新型N-溴烷基取代的(E)-4-氮杂查耳酮溴化物以及N-o-(间和对)-卤代苄基取代的(E)-3'-羟基-4-氮杂查耳酮卤化物的合成。化合物3d、3e、6b、6c和6e对金黄色葡萄球菌和粪肠球菌显示出良好的抗菌活性,对大肠杆菌和肺炎克雷伯菌也有中等活性。