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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Design, synthesis, DFT study and antifungal activity of the derivatives of pyrazolecarboxamide containing thiazole or oxazole ring
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Design, synthesis, DFT study and antifungal activity of the derivatives of pyrazolecarboxamide containing thiazole or oxazole ring

机译:含有噻唑或氧唑环的吡唑甲基酰胺衍生物的设计,合成,DFT研究和抗真菌活性

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摘要

Pyrazolecarboxamide fungicides are one of the most important classes of agricultural fungicides, which belong to succinodehydrogenase inhibitors (SDHIS). To discover new pyrazolecarboxamide analogues with broad spectrum and high activity, a class of new compounds of pyrazole carboxamide derivatives containing thiazole or oxazole ring were designed by scaffold hopping and bioisosterism, and 36 pyrazole carboxamide derivatives with antifungal activity were synthesized. Those compounds were evaluated against five phytopathogenic fungi, Gibberella zeae, Phytophythora capsici, Sclerotonia sclerotiorum, Erysiphe graminis and Puccinia sorghi. The results indicated that most of the compounds displayed good fungicidal activities, especially against E. graminis. Theoretical calculations were carried out at the B3LYP/6-31G (d, p) level and the full geometry optimization was carried out using the 6-31G (d, p) basis set, and the frontier orbital energy, atomic net charges, molecular docking were discussed, and the structure-activity relationships were also studied. (C) 2018 Elsevier Masson SAS. All rights reserved.
机译:吡唑烷酰胺杀菌剂是最重要的农业杀菌剂类别之一,属于琥珀酰基氢酶抑制剂(SDHIS)。为了发现具有广谱和高活性的新的吡唑甲基甲酰胺类似物,通过支架跳跃和生物化学蛋白化设计了一类含有噻唑或氧唑环的吡唑甲酰胺衍生物的新化合物,并且合成了具有抗真菌活性的36个吡唑甲酰胺衍生物。这些化合物评估了五种植物疗法真菌,吉伯拉菌,植物植物,嗜酸盐菌,肠杆菌菌,红霉素麦芽糖素和普昔逊甙SORGHI。结果表明,大多数化合物显示出良好的杀真菌活性,特别是对麦片蛋白。在B3LYP / 6-31G(D,P)水平下进行理论计算,并使用6-31g(d,p)基础集进行全几何优化,以及前轨道能量,原子净电荷,分子讨论了对接,还研究了结构 - 活动关系。 (c)2018年Elsevier Masson SAS。版权所有。

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