Natural Biphenyl-Type Neolignans as Resources of Pesticide Candidates: Assembly, Insecticidal Potency, and Cytotoxicity of Honokiol/Magnolol Analogues of Isoxazoline Hybridization via [3 + 2] Dipolar Cycloaddition

IF 6.2 1区 农林科学 Q1 AGRICULTURE, MULTIDISCIPLINARY Journal of Agricultural and Food Chemistry Pub Date : 2025-02-06 DOI:10.1021/acs.jafc.4c09830
Xiao-Yan Zhi, Hong-Cheng Shi, Xin Yuan, Ming-Tao He, Hua-Wei Li, Yan-Qiong Guo, Hui Cao, Chun Yang
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Abstract

Currently, the development of novel pesticides remains a crucial initiative to address the challenges of agricultural pest management. In pursuit of agrochemical candidates derived from plant natural products (NPs), 76 novel isoxazoline-hybridized honokiol/magnolol analogues were assembled via a [3 + 2] dipolar cycloaddition reaction, and their pesticidal potency and cytotoxicity were evaluated. Bioassays revealed that 13 compounds (5d, 6k, 7bd, 7f, 7g, 8df, 13f, 15d, and 16h) exhibited superior larvicidal activity against Plutella xylostella Linnaeus with LC50 values in the range of 1.75–5.87 μg/mL, outperforming the botanical insecticide rotenone (LC50 = 26.7 μg/mL). Particularly, compounds 7c, 8d, and 15d showed over 11-fold higher larvicidal activity against P. xylostella than against rotenone. Meanwhile, compounds 5i, 6g, 7a, and 8a displayed better growth inhibitory effects on Mythimna separata Walker (LC50 = 0.13, 0.25, 0.34, and 0.35 mg/mL, respectively) compared to rotenone (LC50 = 0.53 mg/mL). Further greenhouse potted-plant assays revealed that compounds 8d and 15d showed superior in vivo control efficacy against P. xylostella compared to rotenone and comparable to tolfenpyrad and also demonstrated good protective effects on plants. Toxicity tests disclosed that these potent compounds exhibited moderate cytotoxicity to the human keratinocyte cell line (HaCaT), indicating a considerably favorable safety profile for skin exposure. Structure–activity relationship (SAR) analysis illustrated the importance of the exposed hydroxyls and newly introduced isoxazoline scaffolds in enhancing the insecticidal activity of these compounds. The novel scaffold, excellent insecticidal potency, and good safety profile position these compounds reported herein as promising leads for further pesticide candidates development. Furthermore, the present work offers valuable insights for advancing the NP-inspired agrochemical innovation.

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天然联苯型新木质素作为候选农药资源:[3 + 2]偶极环加成杂交异恶唑啉的厚朴酚/厚朴酚类似物的组装、杀虫效力和细胞毒性
目前,新型农药的开发仍然是解决农业有害生物管理挑战的关键举措。通过[3 + 2]偶极环加成反应,合成了76种新型异恶唑杂交的厚朴酚/厚朴酚类似物,并对它们的杀虫效力和细胞毒性进行了评价。生物测定结果表明,13种化合物(5d、6k、7b-d、7f、7g、8d-f、13f、15d和16h)对小菜蛾的杀幼虫活性较好,LC50值在1.75 ~ 5.87 μg/mL之间,优于植物性杀虫剂鱼藤酮(LC50 = 26.7 μg/mL)。其中化合物7c、8d和15d对小菜蛾的杀虫活性比鱼藤酮高11倍以上。同时,化合物5i、6g、7a和8a比鱼藤酮(LC50 = 0.53 mg/mL)表现出更好的生长抑制作用(LC50分别为0.13、0.25、0.34和0.35 mg/mL)。进一步的温室盆栽试验表明,化合物8d和15d对小菜蛾的体内防治效果优于鱼藤酮,与苯虫吡酯相当,对植物也有良好的保护作用。毒性试验表明,这些强效化合物对人类角化细胞细胞系(HaCaT)表现出中等的细胞毒性,表明皮肤暴露具有相当有利的安全性。构效关系(SAR)分析表明,暴露的羟基和新引入的异恶唑啉支架在提高这些化合物的杀虫活性方面具有重要意义。这种新型支架、优异的杀虫效力和良好的安全性使这些化合物成为进一步开发候选农药的有希望的线索。此外,目前的工作为推进np启发的农化创新提供了有价值的见解。
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来源期刊
Journal of Agricultural and Food Chemistry
Journal of Agricultural and Food Chemistry 农林科学-农业综合
CiteScore
9.90
自引率
8.20%
发文量
1375
审稿时长
2.3 months
期刊介绍: The Journal of Agricultural and Food Chemistry publishes high-quality, cutting edge original research representing complete studies and research advances dealing with the chemistry and biochemistry of agriculture and food. The Journal also encourages papers with chemistry and/or biochemistry as a major component combined with biological/sensory/nutritional/toxicological evaluation related to agriculture and/or food.
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