Design, synthesis and in vitro antibacterial/antifungal evaluation of novel 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7(1-piperazinyl)quinoline-3-carboxylic acid derivatives

被引:40
|
作者
Yu, Zhiyi [2 ]
Shi, Guanying [1 ]
Sun, Qiu [2 ]
Jin, Hong [3 ]
Teng, Yun [1 ]
Tao, Ke [1 ]
Zhou, Guoping [2 ]
Liu, Wei [2 ]
Wen, Fang [3 ]
Hou, Taiping [1 ]
机构
[1] Sichuan Univ, Key Lab Bioresource & Ecoenvironm, Minist Educ, Coll Life Sci, Chengdu 610064, Sichuan, Peoples R China
[2] Sichuan Univ, W China Sch Pharm, Chengdu 610064, Peoples R China
[3] Sichuan Univ, Key Lab Green Chem & Technol, Minist Educ, Coll Chem, Chengdu 610064, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Norfloxacin; Carboxylic acid amide; Synthesis; Antibacterial activity; Antifungal activity;
D O I
10.1016/j.ejmech.2009.05.028
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7(1-piperazinyl)quinoline-3-carboxylic acid (norfloxacin) derivatives were prepared according to the principle of combinating bioactive substructures and tested for their activities against five plant pathogenic bacteria and three fungi in vitro. The preliminary bioassays indicated that almost all synthesized target compounds retained the antibacterial activities of norfloxacin and had some antifungal activities as carboxylic acid amide compounds. The activities of compounds 1 and 22 against Xanthomonas oryzae were better than norfloxacin and all tested compounds had better antibacterial activities as compared to the agricultural streptomycin sulfate (a commercial bactericide) against X oryzae, Xanthomonas axonopodis and Erwinia aroideae. Additionally, compounds 2 and 20 displayed good antifungal activities against Rhizoctonia solani and their inhibition of growth reached 83% and 94% respectively at the concentration of 200 mg/L (C) 2009 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:4726 / 4733
页数:8
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