<i>N</i>‐Methoxy Pyrazole‐4‐Carboxamide Derivatives: Synthesis, Spectral Analyses, Antifungal Activity, In Silico Molecular Docking, <scp>ADMET,</scp> and <scp>DFT</scp> Studies

ABSTRACT 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 1 H NMR, 13 C 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 EC 50 is 7.80 μg/mL, which is comparable with the positive control bixafen (EC 50 = 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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Publication Details

Journal
Journal of Heterocyclic Chemistry
Published
2024-10-02
DOI
https://doi.org/10.1002/jhet.4903
Citations
3
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.75

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article

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

Li‐Jing Min, Bin Wang, Liqin Zhang, Xing‐Hai Liu et al.
3 citations
Journal of Heterocyclic Chemistry
Synthesis and biological activity
0.75
article

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

Li‐Jing Min, Bin Wang, Liqin Zhang, Xing‐Hai Liu, Hong‐Ke Wu, Zi‐Ting Luo
article en
3 citations

Abstract

ABSTRACT 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 1 H NMR, 13 C 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 EC 50 is 7.80 μg/mL, which is comparable with the positive control bixafen (EC 50 = 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.

Journal of Heterocyclic ChemistryVol. 61(12)
Huzhou Normal University (CN), Zhejiang University of Technology (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China, Natural Science Foundation of Zhejiang Province
Openalex Percentile: Top 32%
Synthesis and biological activity
0.75
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<i>N</i>‐Methoxy Pyrazole‐4‐Carboxamide Derivatives: Synthesis, Spectral Analyses, Antifungal Activity, In Silico Molecular Docking, <scp>ADMET,</scp> and <scp>DFT</scp> Studies — Li‐Jing Min, Bin Wang, et al. · Journal of Heterocyclic Chemistry (2024) | TGRS Research Map | TGRS