Discovery of NovelIsoxazoline Derivatives ContainingPyrazolamide Fragment as Insecticidal Candidates

Lepidopteran species cause significant harm to agricultural yields and food quality. In this study, a series of innovative isoxazoline derivatives incorporating pyrazolamide moieties were carefully designed and synthesized as potential insecticidal agents. Among these, compound <b>F16</b> demonstrated an LC<sub>50</sub> value of 0.01 mg/L against Plutella xylostella, surpassing that of the lead compound fluxametamide (LC<sub>50</sub> = 0.15 mg/L). Furthermore, <b>F16</b> exhibited broad-spectrum insecticidal activity against Pyrausta nubilalis, Spodoptera frugiperda, Chilo suppressalis, Aphis craccivora, and Sogatella furcifera. Notably, <b>F16</b> possessed low toxicity against Danio rerio, whereas fluxametamide displayed moderate toxicity. Furthermore, molecular docking analysis demonstrated that the potent insecticidal activity of <b>F16</b> is likely mediated by its specific interactions with γ-GABA receptors primarily through the formation of hydrogen bonds with key residues. Density functional theory calculations and molecular electrostatic potentials were also performed to gain insights into the insecticidal behavior of <b>F16</b>. These findings suggest that <b>F16</b> is a promising candidate for further investigation as a novel pesticide.

Publication Details

Journal
Figshare
Published
2025-03-07
DOI
https://doi.org/10.1021/acs.jafc.4c13106.s001
Primary Topic
Insect-Plant Interactions and Control
Type
article
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article

Discovery of NovelIsoxazoline Derivatives ContainingPyrazolamide Fragment as Insecticidal Candidates

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Insect-Plant Interactions and Control
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Discovery of NovelIsoxazoline Derivatives ContainingPyrazolamide Fragment as Insecticidal Candidates

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Abstract

Lepidopteran species cause significant harm to agricultural yields and food quality. In this study, a series of innovative isoxazoline derivatives incorporating pyrazolamide moieties were carefully designed and synthesized as potential insecticidal agents. Among these, compound <b>F16</b> demonstrated an LC<sub>50</sub> value of 0.01 mg/L against Plutella xylostella, surpassing that of the lead compound fluxametamide (LC<sub>50</sub> = 0.15 mg/L). Furthermore, <b>F16</b> exhibited broad-spectrum insecticidal activity against Pyrausta nubilalis, Spodoptera frugiperda, Chilo suppressalis, Aphis craccivora, and Sogatella furcifera. Notably, <b>F16</b> possessed low toxicity against Danio rerio, whereas fluxametamide displayed moderate toxicity. Furthermore, molecular docking analysis demonstrated that the potent insecticidal activity of <b>F16</b> is likely mediated by its specific interactions with γ-GABA receptors primarily through the formation of hydrogen bonds with key residues. Density functional theory calculations and molecular electrostatic potentials were also performed to gain insights into the insecticidal behavior of <b>F16</b>. These findings suggest that <b>F16</b> is a promising candidate for further investigation as a novel pesticide.

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