首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Evolution from Natural β-Carboline Alkaloids to Obtain 1,2,4,9-tetrahydro-3-thia-9-aza-fluorene Derivatives as Potent Fungicidal Agents against Rhizoctonia solani
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Evolution from Natural β-Carboline Alkaloids to Obtain 1,2,4,9-tetrahydro-3-thia-9-aza-fluorene Derivatives as Potent Fungicidal Agents against Rhizoctonia solani

机译:从天然β-咔啉生物碱到获得1,2,4,9-四氢-3-硫杂-9-氮杂芴衍生物作为抗枯萎病有效杀菌剂的演变

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摘要

Rice sheath blight, caused by Rhizoctonia solani, is a globally important rice disease and the increasing resistance of this pathogen highlights the need for new active compounds against rice sheath blight. In this study, natural β-carboline alkaloids were optimized to obtain a series of 1,2,4,9-tetrahydro-3-thia-9-aza-fluorene derivatives and evaluated for their fungicidal activity and mode of action against R. solani. Of these compounds, 18 exhibited significant in vitro fungicidal activity against R. solani, with an EC50 value of 2.35 μg/mL, and was more active than validamycin A. In vivo bioassay also demonstrated that 18 displayed superior protective and curative activities as compared to validamycin A. Mechanistically, 18 not only induced the loss of mitochondrial membrane potential and accumulation of reactive oxygen species, but also interfered with DNA synthesis. Therefore, compound 18 displayed pronounced in vitro and in vivo fungicidal activity against R. solani and could be used as a potential candidate for the control of rice sheath blight.
机译:由茄状枯萎病引起的稻鞘枯萎病是全球重要的水稻疾病,这种病原体的抗药性不断增强,凸显了对新型活性化合物对稻鞘枯萎病的需求。在这项研究中,天然β-咔啉生物碱进行了优化,以获得一系列的1,2,4,9-四氢-3-thia-9-氮杂芴芴衍生物,并评估了它们的杀真菌活性和对sol。solani的作用方式。 。在这些化合物中, 18 对R. solani表现出显着的体外杀真菌活性,EC50值为2.35μg/ mL,并且比有效霉素A更具活性。体内生物测定法也表明与有效霉素A相比,18 具有更好的保护和治疗作用。 18 在机理上不仅引起线粒体膜电位的丧失和活性氧的积累,还干扰了DNA的合成。因此,化合物 18 表现出明显的对茄红假单胞菌的体外和体内杀真菌活性,可作为控制稻瘟病的潜在候选物。

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