1,2,4-Triazole-conjugated Fluoroquinolones as Potential Candidates for New Antibacterial Agents

被引:0
作者
Cebeci, Yildiz Uygun [1 ]
Karaoglu, Senguel Alpay [2 ]
机构
[1] Kirklareli Univ, Dept Chem, Kirklareli, Turkiye
[2] Recep Tayyip Erdogan Univ, Dept Biol, Rize, Turkiye
关键词
Fluoroquinolones; hybride molecule; triazole; mannich base; schiff base; antibacterial; MANNICH-BASES; ANTIMICROBIAL EVALUATION; DERIVATIVES; ANTICANCER; SCHIFF; DESIGN; ORGANOCATALYSIS; QUINOLONES; CHEMISTRY; ALDOL;
D O I
10.2174/0115701786270260231215101046
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In this study, synthesis of 1,2,4 triazole-fluoroquinolone hybrid compounds was realized. 7a-d hybrid compound was obtained as a result of mannich reaction with 6a-b triazole compounds norfloxacin and ciprofloxacin. 1H-NMR, 13C-NMR, Mass Spectrometry and Elemental Analysis confirmed the structures of all synthesized compounds. The antimicrobial activities of all compounds were investigated, and it was observed that 7a-d compounds, which are mannich bases, showed excellent activity.
引用
收藏
页码:669 / 676
页数:8
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