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新型含吡啶鎓部分吲哚衍生物的合成、抗菌活性及作用机制。

Synthesis, Antibacterial Activity, and Mechanisms of Novel Indole Derivatives Containing Pyridinium Moieties.

机构信息

State Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Research and Development Center for Fine Chemicals, Guizhou University, Huaxi District, Guiyang 550025, China.

出版信息

J Agric Food Chem. 2022 Oct 5;70(39):12341-12354. doi: 10.1021/acs.jafc.2c04213. Epub 2022 Sep 22.

Abstract

The development of effective antibacterial agents equipped with novel action modes and unique skeletons starting from natural compounds serves as an important strategy in the modern pesticide industry. Disclosed here are a series of novel indole derivatives containing pyridinium moieties and their antibacterial activity evaluation against two prevalent phytopathogenic bacteria, pv. () and pv. (). A three-dimensional (3D)-QSAR model was adopted to discover higher activity like title compounds based on the antibacterial activity of the tested compounds. Compound was consequently designed, and it displayed higher antibacterial activity as expected with the half-maximal effective concentration EC values of 1.0 and 1.9 μg/mL for and , respectively, which were better than those of the commercial drug thiodiazole copper (TC) (72.9 and 87.5 μg/mL). Under greenhouse conditions, the results of a rice pot experiment indicated that the protective and curative activities of compound against rice bacterial leaf streak (BLS) and rice bacterial blight (BLB) were 45.0 and 44.0% and 42.0 and 39.3%, respectively, which were better than those of the commercial agent thiodiazole copper (38.0 and 37.9%, 38.6 and 37.0%) as well. Scanning electron microscopy images, defense enzyme activity tests, and proteomic techniques were utilized in a preliminary mechanism study, suggesting that compound shall modulate and interfere with the physiological processes and functions of pathogenic bacteria.

摘要

从天然化合物出发,开发具有新型作用模式和独特骨架的有效抗菌剂,是现代农药行业的重要策略。本文公开了一系列含有吡啶鎓部分的新型吲哚衍生物及其对两种流行的植物病原菌 pv. () 和 pv. () 的抗菌活性评价。采用三维(3D)QSAR 模型,基于所测试化合物的抗菌活性,发现了更高活性的类似标题化合物。因此设计了化合物 ,并期望其具有更高的抗菌活性,其对 和 的半数最大有效浓度 EC 值分别为 1.0 和 1.9 μg/mL,优于商业药物噻二唑铜 (TC)(72.9 和 87.5 μg/mL)。在温室条件下,水稻盆栽试验的结果表明,化合物 对水稻细菌性条斑病(BLS)和水稻细菌性疫病(BLB)的保护和治疗活性分别为 45.0%和 44.0%,以及 42.0%和 39.3%,优于商业药剂噻二唑铜(38.0%和 37.9%,38.6%和 37.0%)。扫描电子显微镜图像、防御酶活性测试和蛋白质组学技术的初步机制研究表明,化合物 可以调节和干扰病原菌的生理过程和功能。

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