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Synthesis and Biological Activity Evaluation of 1,2,3- Thiadiazole Derivatives as Potential Elicitors with Highly Systemic Acquired Resistance

机译:1,2,3-噻二唑衍生物的合成及其生物活性评估

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Elicitors provide a broad spectrum of systemic acquired resistance by altering the physical and physiological status of the host plants and, therefore, are among the most successful directions in modern pesticide development for plant protection. To develop a novel elicitor with highly systemic acquired resistance, two series of thiazole- and oxadiazole-containing thiadiazole derivatives were rationally designed and synthesized according to the principle of combination of bioactive substructures in this work. Their structures were characterized by ~1H nuclear magnetic resonance (NMR), infrared (IR), high-resolution mass spectrometry (HRMS), or elemental analysis. Their potential systemic acquired resistance as an elicitor was also evaluated; bioassay results indicated that, among the 23 compounds synthesized, three compounds, 10a, 10d, and 12b, displayed better systemic acquired resistance than the positive control, tiadinil, a commercialized 1,2,3-thiadiazole-based elicitor. In addition, three other compounds, 10f, 12c, and 12j, exhibited a certain degree of fungus growth inhibition in vitro or - in vivo. Our results demonstrated that, in combination of bioactive substructures is an interesting exploration for novel pesticide development, thiazole-and oxadiazole-containing thiadiazole derivatives are potential elicitors with good systemic acquired resistance.
机译:诱导剂通过改变寄主植物的生理和生理状况提供广泛的系统获得性抗性,因此,是现代农药开发中用于植物保护的最成功的方向之一。为了开发具有高系统获得性抗药性的新型激发子,在这项工作中,根据生物活性亚结构的组合原理,合理设计和合成了两个系列的含噻唑和恶二唑的噻二唑衍生物。它们的结构通过〜1H核磁共振(NMR),红外(IR),高分辨率质谱(HRMS)或元素分析来表征。还评估了它们作为引发剂的潜在系统性获得性抵抗力;生物测定结果表明,在合成的23种化合物中,三种化合物10a,10d和12b表现出比阳性对照噻菌胺(一种以1,2,3-噻二唑为基础的激发剂)更好的全身获得性抗药性。此外,其他三种化合物10f,12c和12j在体外或体内显示出一定程度的真菌生长抑制作用。我们的结果表明,结合生物活性亚结构是新型农药开发的有趣探索,噻唑和含恶二唑的噻二唑衍生物是具有良好系统获得性耐药性的潜在诱因。

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