n -甲氧基吡唑-4-羧基酰胺衍生物:合成、光谱分析、抗真菌活性、硅分子对接、ADMET和DFT研究

IF 2 3区 化学 Q2 CHEMISTRY, ORGANIC
Zi-Ting Luo, Bin Wang, Hong-Ke Wu, Li-Jing Min, Li-Qin Zhang, Xing-Hai Liu
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引用次数: 0

摘要

琥珀酸脱氢酶抑制剂(SDHI)是防治粮食病害的重要杀菌剂。为此,设计并合成了一系列具有n -甲氧基的新型吡唑-4-甲酰胺衍生物。所有目标化合物均通过1H NMR、13C NMR和HRMS进行了表征。x射线衍射进一步证实了化合物3c在三斜体系中结晶,空间群P-1, Z = 2。结果表明,在50 ppm条件下,大部分化合物对菌核菌具有良好的抑菌活性。其中化合物3h的EC50值为7.80 μg/mL,与阳性对照bixafen (EC50值为6.70 μg/mL)相当。此外,本研究还对化合物3h、3k和两种商业化sdis异氟西拉姆和吡氟醚的理化性质、分子对接模拟、ADMET分析和DFT进行了研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

N-Methoxy Pyrazole-4-Carboxamide Derivatives: Synthesis, Spectral Analyses, Antifungal Activity, In Silico Molecular Docking, ADMET, and DFT Studies

N-Methoxy Pyrazole-4-Carboxamide Derivatives: Synthesis, Spectral Analyses, Antifungal Activity, In Silico Molecular Docking, ADMET, and DFT Studies

Succinate dehydrogenase inhibitor (SDHI) is an important fungicide to control grain diseases. For this reason, a series of novel pyrazole-4-carboxamide derivatives with an N-methoxy group were designed and synthesized. All the target compounds were characterized by 1H NMR, 13C NMR, and HRMS. The compound 3c was further confirmed by X-ray diffraction, which crystallized in the triclinic system, space group P-1, Z = 2. The fungicidal activity results indicated that most of these compounds possessed good activity against Sclerotinia sclerotiorum at 50 ppm. Especially, compound 3h exhibited the best activity with the EC50 is 7.80 μg/mL, which is comparable with the positive control bixafen (EC50 = 6.70 μg/mL). Furthermore, the physicochemical properties, molecular docking simulation, ADMET analyses, DFT of compounds 3h, 3k and two commercial SDHIs, isoflucypram and pydiflumetofen, were investigated in this study.

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来源期刊
Journal of Heterocyclic Chemistry
Journal of Heterocyclic Chemistry 化学-有机化学
CiteScore
5.20
自引率
4.20%
发文量
177
审稿时长
3.9 months
期刊介绍: The Journal of Heterocyclic Chemistry is interested in publishing research on all aspects of heterocyclic chemistry, especially development and application of efficient synthetic methodologies and strategies for the synthesis of various heterocyclic compounds. In addition, Journal of Heterocyclic Chemistry promotes research in other areas that contribute to heterocyclic synthesis/application, such as synthesis design, reaction techniques, flow chemistry and continuous processing, multiphase catalysis, green chemistry, catalyst immobilization and recycling.
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