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Bioactive Quinic Acid Derivatives from Ageratina adenophora

机译:紫茎泽兰的生物活性奎尼酸衍生物

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摘要

A novel quinic acid derivative, 5-O-trans-o-coumaroylquinic acid methyl ester (>1), together with three known ones, chlorogenic acid methyl ester (>2), macranthoin F (>3) and macranthoin G (>4), were isolated from the aerial parts of the invasive plant Ageratina adenophora (Spreng.). The structure of new compound >1 was elucidated on the basis of extensive spectroscopic analysis, including 1D- and 2D-NMR techniques. Compounds >2–>4 were isolated from plant A. adenophora for the first time. All the compounds showed in vitro antibacterial activity toward five assayed bacterial strains, especially >3 and >4, which showed in vitro antibacterial activity against Salmonella enterica with MIC values of 7.4 and 14.7 μM, respectively. Compound >1 was further found to display in vitro anti-fungal activity against spore germination of Magnaporthe grisea with an IC50 value 542.3 µM. These four compounds were also tested for their antioxidant activity against DPPH (1,1-diphenyl-2-picrylhydrazyl) radical.
机译:一种新颖的奎尼酸衍生物5-O-反式-邻-香豆酰基奎宁酸甲酯(> 1 )和三种已知的绿原酸甲酯(> 2 ),从侵染植物紫茎泽兰(Spreng。)的气生部中分离出macranthoin F(> 3 )和macranthoin G(> 4 )。在广泛的光谱分析(包括1D-NMR和2D-NMR技术)的基础上,阐明了新化合物> 1 的结构。化合物> 2 – > 4 是首次从植物紫茎泽兰中分离出来。所有化合物均对五种测定的细菌菌株具有体外抗菌活性,尤其是> 3 和> 4 ,它们对肠炎沙门氏菌均具有体外抗菌活性,MIC值为7.4和14.7μM。 , 分别。进一步发现化合物> 1 具有体外抗真菌活性,可用于稻瘟病菌的孢子萌发,IC50值为542.3 µM。还测试了这四种化合物对DPPH(1,1-二苯基-2-吡啶并肼基)自由基的抗氧化活性。

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