首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >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.
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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.

机译:新型1-乙基-6-氟-1,4-二氢-4-氧代-7(1-哌嗪基)喹啉-3-羧酸衍生物的设计,合成及体外抗菌/抗真菌评价。

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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 200mg/L.
机译:根据结合生物活性亚结构的原理,制备了一系列1-乙基-6-氟-1,4-二氢-4-氧代-7(1-哌嗪基)喹啉-3-羧酸(诺氟沙星)衍生物,并对其进行了测试。它们在体外对五种植物病原菌和三种真菌的活性。初步的生物测定结果表明,几乎所有合成的目标化合物都保留了诺氟沙星的抗菌活性,并具有一些作为羧酸酰胺化合物的抗真菌活性。与农用硫酸链霉素硫酸盐(商业杀菌剂)相比,化合物1和22对米生黄单胞菌的活性要好于诺氟沙星,并且所有测试的化合物都具有更好的抗菌活性。此外,化合物2和20对200毫克/升的浓度对茄红枯萎病菌表现出良好的抗真菌活性,它们的生长抑制分别达到83%和94%。

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