{"title":"Design, Synthesis and Insecticidal Activity of Novel m-diamide Compounds Containing Sulfur.","authors":"Pengmian Huang, Hualan Yang, Minghui Wu, Liqi Zhou, Zihan Huang, Jiyong Liu","doi":"10.1002/cbdv.202500230","DOIUrl":null,"url":null,"abstract":"<p><p>To find efficient insecticides with novel structures, 16 novel m-diamides compounds containing sulfur were designed and synthesized based on the principle of biologically active factor splicing with cyproflanilide as the lead compound. Preliminary biological assay data showed that some of the target compounds exhibited insecticidal activity above 90% against Mythimna separata at 0.01 mg/L and Aphis craccivora at 100 mg/L, which were better than cyproflanilide. Meanwhile, most compounds still maintain 100% mortality at 1 mg/L for Plutella xylostella. In particular, compounds 5c, 5e, 5f, and 5g revealed excellent activities against Plutella xylostella, Mythimna separata and Aphis craccivora, exhibiting efficient and broad-spectrum insecticidal activity. Additionally, the interaction between the metabolites of cyproflanilide, compound 5g and GABA receptor protein was studied by molecular docking method. The results showed that they could be stably bound to the potential active cavity in the protein to form a protein-ligand complex, thus showing excellent insecticidal activity, which is consistent with the data of excellent insecticidal activity of compounds. This work showed that sulfur-containing compounds might provide certain clues for structure optimization for the development of new insecticides.</p>","PeriodicalId":9878,"journal":{"name":"Chemistry & Biodiversity","volume":" ","pages":"e202500230"},"PeriodicalIF":2.3000,"publicationDate":"2025-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry & Biodiversity","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/cbdv.202500230","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
To find efficient insecticides with novel structures, 16 novel m-diamides compounds containing sulfur were designed and synthesized based on the principle of biologically active factor splicing with cyproflanilide as the lead compound. Preliminary biological assay data showed that some of the target compounds exhibited insecticidal activity above 90% against Mythimna separata at 0.01 mg/L and Aphis craccivora at 100 mg/L, which were better than cyproflanilide. Meanwhile, most compounds still maintain 100% mortality at 1 mg/L for Plutella xylostella. In particular, compounds 5c, 5e, 5f, and 5g revealed excellent activities against Plutella xylostella, Mythimna separata and Aphis craccivora, exhibiting efficient and broad-spectrum insecticidal activity. Additionally, the interaction between the metabolites of cyproflanilide, compound 5g and GABA receptor protein was studied by molecular docking method. The results showed that they could be stably bound to the potential active cavity in the protein to form a protein-ligand complex, thus showing excellent insecticidal activity, which is consistent with the data of excellent insecticidal activity of compounds. This work showed that sulfur-containing compounds might provide certain clues for structure optimization for the development of new insecticides.
期刊介绍:
Chemistry & Biodiversity serves as a high-quality publishing forum covering a wide range of biorelevant topics for a truly international audience. This journal publishes both field-specific and interdisciplinary contributions on all aspects of biologically relevant chemistry research in the form of full-length original papers, short communications, invited reviews, and commentaries. It covers all research fields straddling the border between the chemical and biological sciences, with the ultimate goal of broadening our understanding of how nature works at a molecular level.
Since 2017, Chemistry & Biodiversity is published in an online-only format.