{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,14]],"date-time":"2026-10-14T08:44:18Z","timestamp":1791967458346,"version":"4.3.4"},"reference-count":33,"publisher":"Wiley","license":[{"start":{"date-parts":[[2026,10,14]],"date-time":"2026-10-14T00:00:00Z","timestamp":1791936000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2026,10,14]],"date-time":"2026-10-14T00:00:00Z","timestamp":1791936000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"funder":[{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"publisher","award":["32502551"],"award-info":[{"award-number":["32502551"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["scijournals.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Pest Management Science"],"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>BACKGROUND<\/jats:title>\n                    <jats:p>Lepidopteran pests have developed severe resistance to diamide insecticides, posing a huge challenge to effective pest control, necessitating the development of novel insecticides to achieve the effective comprehensive management of pests. Forty\u2010two novel derivatives bearing substituted benzylamine moieties with chlorantraniliprole (CHL) as the lead compound were precisely design, synthesized, and evaluated for insecticidal activities against three Lepidopteran pests.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>RESULTS<\/jats:title>\n                    <jats:p>\n                      The bioassay results showed that the LC\n                      <jats:sub>50<\/jats:sub>\n                      values of compounds\n                      <jats:bold>A26<\/jats:bold>\n                      and\n                      <jats:bold>A40<\/jats:bold>\n                      against\n                      <jats:italic>Mythimna separata<\/jats:italic>\n                      were 0.080 and 0.163\u2009mg\u2009L\n                      <jats:sup>\u22121<\/jats:sup>\n                      , respectively, comparable to that of CHL (LC\n                      <jats:sub>50<\/jats:sub>\n                      0.124\u2009mg\u2009L\n                      <jats:sup>\u22121<\/jats:sup>\n                      ). For\n                      <jats:italic>Plutella xylostella<\/jats:italic>\n                      , the LC\n                      <jats:sub>50<\/jats:sub>\n                      values of\n                      <jats:bold>A16<\/jats:bold>\n                      and\n                      <jats:bold>A40<\/jats:bold>\n                      were 0.041 and 0.048\u2009mg\u2009L\n                      <jats:sup>\u22121<\/jats:sup>\n                      , respectively, equivalent to that of CHL (LC\n                      <jats:sub>50<\/jats:sub>\n                      0.049\u2009mg\u2009L\n                      <jats:sup>\u22121<\/jats:sup>\n                      ). Additionally, compound\n                      <jats:bold>A40<\/jats:bold>\n                      showed insecticidal activity against\n                      <jats:italic>Spodoptera frugiperda<\/jats:italic>\n                      comparable to that of CHL (LC\n                      <jats:sub>5<\/jats:sub>\n                      0.279 vs 0.174\u2009mg\u2009L\n                      <jats:sup>\u22121<\/jats:sup>\n                      ) and exhibited significantly superior efficacy against the resistant strain (LC\n                      <jats:sub>50<\/jats:sub>\n                      75.83 vs 141.75\u2009mg\u2009L\n                      <jats:sup>\u22121<\/jats:sup>\n                      ). These results indicate that\n                      <jats:bold>A40<\/jats:bold>\n                      exhibits excellent insecticidal efficacy against Lepidopteran pests. Calcium imaging experiments suggested that compound\n                      <jats:bold>A40<\/jats:bold>\n                      targets the insect ryanodine receptors, which was further validated by transcriptome analysis and molecular docking assays.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>CONCLUSIONS<\/jats:title>\n                    <jats:p>This research will provide valuable insights for the development of novel diamide insecticides containing benzylamine scaffolds. \u00a9 2026 Society of Chemical Industry.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/ps.71351","type":"journal-article","created":{"date-parts":[[2026,10,14]],"date-time":"2026-10-14T07:44:56Z","timestamp":1791963896000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Discovery of diamide derivatives bearing a flexible substituted benzylamine moiety as potential ryanodine receptor activator"],"prefix":"10.1002","author":[{"given":"Fengyu","family":"Li","sequence":"first","affiliation":[{"name":"MARA Key Laboratory of Sustainable Crop Production in the Middle Reaches of the Yangtze River (Co\u2010construction by Ministry and Pro vince)\/Hubei Key Laboratory of Waterlogging Disaster and Agricultural Use of Wetland, College of Agriculture Yangtze University  Jingzhou China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jiaying","family":"Duan","sequence":"additional","affiliation":[{"name":"MARA Key Laboratory of Sustainable Crop Production in the Middle Reaches of the Yangtze River (Co\u2010construction by Ministry and Pro vince)\/Hubei Key Laboratory of Waterlogging Disaster and Agricultural Use of Wetland, College of Agriculture Yangtze University  Jingzhou China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hongzhou","family":"Liu","sequence":"additional","affiliation":[{"name":"MARA Key Laboratory of Sustainable Crop Production in the Middle Reaches of the Yangtze River (Co\u2010construction by Ministry and Pro vince)\/Hubei Key Laboratory of Waterlogging Disaster and Agricultural Use of Wetland, College of Agriculture Yangtze University  Jingzhou China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Changxu","family":"Lu","sequence":"additional","affiliation":[{"name":"MARA Key Laboratory of Sustainable Crop Production in the Middle Reaches of the Yangtze River (Co\u2010construction by Ministry and Pro vince)\/Hubei Key Laboratory of Waterlogging Disaster and Agricultural Use of Wetland, College of Agriculture Yangtze University  Jingzhou China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yunqi","family":"Ding","sequence":"additional","affiliation":[{"name":"MARA Key Laboratory of Sustainable Crop Production in the Middle Reaches of the Yangtze River (Co\u2010construction by Ministry and Pro vince)\/Hubei Key Laboratory of Waterlogging Disaster and Agricultural Use of Wetland, College of Agriculture Yangtze University  Jingzhou China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Zhijing","family":"Cao","sequence":"additional","affiliation":[{"name":"MARA Key Laboratory of Sustainable Crop Production in the Middle Reaches of the Yangtze River (Co\u2010construction by Ministry and Pro vince)\/Hubei Key Laboratory of Waterlogging Disaster and Agricultural Use of Wetland, College of Agriculture Yangtze University  Jingzhou China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lixia","family":"Xiong","sequence":"additional","affiliation":[{"name":"State Key Laboratory of Elemento\u2010Organic Chemistry, College of Chemistry Nankai University  Tianjin China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2739-7197","authenticated-orcid":false,"given":"Jinzhou","family":"Ren","sequence":"additional","affiliation":[{"name":"MARA Key Laboratory of Sustainable Crop Production in the Middle Reaches of the Yangtze River (Co\u2010construction by Ministry and Pro vince)\/Hubei Key Laboratory of Waterlogging Disaster and Agricultural Use of Wetland, College of Agriculture Yangtze University  Jingzhou China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Zhihong","family":"Xu","sequence":"additional","affiliation":[{"name":"MARA Key Laboratory of Sustainable Crop Production in the Middle Reaches of the Yangtze River (Co\u2010construction by Ministry and Pro vince)\/Hubei Key Laboratory of Waterlogging Disaster and Agricultural Use of Wetland, College of Agriculture Yangtze University  Jingzhou China"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2026,10,14]]},"reference":[{"key":"e_1_2_8_2_1","doi-asserted-by":"crossref","first-page":"411","DOI":"10.1083\/jcb.127.2.411","article-title":"Cryo\u2010electron microscopy and three\u2010dimensional reconstruction of the calcium release channel\/ryanodine receptor from skeletal muscle","volume":"127","author":"Radermacher M","year":"1994","journal-title":"J Cell Biol"},{"key":"e_1_2_8_3_1","doi-asserted-by":"crossref","first-page":"9485","DOI":"10.1074\/jbc.275.13.9485","article-title":"Three\u2010dimensional structure of ryanodine receptor isoform three in two conformational states as visualized by cryo\u2010electron microscopy","volume":"275","author":"Sharma MR","year":"2000","journal-title":"J Biol Chem"},{"key":"e_1_2_8_4_1","doi-asserted-by":"crossref","first-page":"26","DOI":"10.2174\/1381612827666210902150224","article-title":"Ryanodine receptor as insecticide target","volume":"28","author":"Samurkas A","year":"2022","journal-title":"Curr Pharm Des"},{"key":"e_1_2_8_5_1","doi-asserted-by":"crossref","first-page":"4898","DOI":"10.1016\/j.bmcl.2005.08.034","article-title":"Insecticidal anthranilic diamides: a new class of potent ryanodine receptor activators","volume":"15","author":"Lahm GP","year":"2005","journal-title":"Bioorg Med Chem Lett"},{"key":"e_1_2_8_6_1","doi-asserted-by":"crossref","first-page":"6274","DOI":"10.1016\/j.bmcl.2007.09.012","article-title":"Rynaxypyr: a new insecticidal anthranilic diamide that acts as a potent and selective ryanodine receptor activator","volume":"17","author":"Lahm GP","year":"2007","journal-title":"Bioorg Med Chem Lett"},{"key":"e_1_2_8_7_1","doi-asserted-by":"crossref","first-page":"23916","DOI":"10.1021\/acs.jafc.5c04747","article-title":"Design, synthesis, insecticidal activities, and structure\u2212activity relationship of phenylpyrazole derivatives incorporating 1,2,4\u2010oxadiazole moiety","volume":"73","author":"Du SQ","year":"2025","journal-title":"J Agric Food Chem"},{"key":"e_1_2_8_8_1","doi-asserted-by":"crossref","first-page":"5483","DOI":"10.1021\/jf4012467","article-title":"Synthesis, insecticidal activities, and SAR studies of novel pyridylpyrazole acid derivatives based on amide bridge modification of anthranilic diamide insecticides","volume":"61","author":"Wang BL","year":"2013","journal-title":"J Agric Food Chem"},{"key":"e_1_2_8_9_1","doi-asserted-by":"crossref","first-page":"2827","DOI":"10.1021\/acs.jafc.2c07680","article-title":"Anthranilic diamides containing monofluoroalkene amide linkers as potential insect RyR activators: design, synthesis, bio\u2010evaluation, and computational study","volume":"71","author":"Yang G","year":"2023","journal-title":"J Agric Food Chem"},{"key":"e_1_2_8_10_1","doi-asserted-by":"crossref","first-page":"3074","DOI":"10.1002\/ps.8678","article-title":"Computer\u2010aided design of novel anthranilic diamides containing fluorinated alkoxy groups as potential ryanodine receptor insecticides","volume":"81","author":"Chen Y","year":"2025","journal-title":"Pest Manag Sci"},{"key":"e_1_2_8_11_1","unstructured":"LahmGP Preparation of novel anthranilamides useful for controlling invertebrate pests. WO 2006023783 A1(2006)."},{"key":"e_1_2_8_12_1","unstructured":"HughesKA LahmGP SelbyTPandStevensonTM Cyano anthranilamide insecticides. WO 04067528 A1(2004)."},{"key":"e_1_2_8_13_1","unstructured":"JeanguenatAandO'sullivanAC Anthranilamide derivatives as insecticides. WO 2006061200 A1(2006)."},{"key":"e_1_2_8_14_1","unstructured":"MuehlebachMandCraigGW N\u2010cyanoalkyl anthranilamides as insecticides. WO 2008064891 A1(2006)."},{"key":"e_1_2_8_15_1","unstructured":"KoerberKandPohlmanM Use of cyclaniliprole on cultivated plants. WO 2016146586 A1(2016)."},{"key":"e_1_2_8_16_1","doi-asserted-by":"crossref","first-page":"12203","DOI":"10.1021\/acs.jafc.2c03997","article-title":"Discovery of azo\u2010aminopyrimidines as novel and potent chitinase of Chi\u2010h inhibitors via structure\u2010based virtual screening and rational lead optimization","volume":"70","author":"Dong L","year":"2022","journal-title":"J Agric Food Chem"},{"key":"e_1_2_8_17_1","doi-asserted-by":"crossref","first-page":"16112","DOI":"10.1021\/acs.jafc.4c01033","article-title":"Design, synthesis, bioactivity, and tentative exploration of action mode for benzyl ester\u2010containing derivatives","volume":"72","author":"Yuan QL","year":"2024","journal-title":"J Agric Food Chem"},{"key":"e_1_2_8_18_1","unstructured":"YuchiZG MaRF MaD JiangH ZhangJ LiZMet al. New use of compound. WO 2022007875 A1(2022)."},{"key":"e_1_2_8_19_1","unstructured":"XuLZ ZhangHQ LiHP HuangXSandWangMH Anthranilamide arthropodicide treatment. US 9173400 B2(2015)."},{"key":"e_1_2_8_20_1","doi-asserted-by":"crossref","first-page":"2022","DOI":"10.1002\/ps.6826","article-title":"Design, synthesis and biological activity of diamide compounds based on 3\u2010substituent of the pyrazole ring","volume":"78","author":"Zhang Z","year":"2022","journal-title":"Pest Manag Sci"},{"key":"e_1_2_8_21_1","doi-asserted-by":"crossref","first-page":"5442","DOI":"10.1002\/ps.70649","article-title":"Morpholine ring facilitates antiviral potency of pyrazoline acylhydrazone against TMV: design, synthesis, and mechanistic study","volume":"82","author":"Liao AJ","year":"2026","journal-title":"Pest Manag Sci"},{"key":"e_1_2_8_22_1","article-title":"Design, synthesis, and antiviral activity of novel piperidine\u2010containing pyrazoleamide derivatives","volume":"82","author":"Sun W","year":"2026","journal-title":"Pest Manag Sci"},{"key":"e_1_2_8_23_1","doi-asserted-by":"crossref","first-page":"10453","DOI":"10.1021\/acs.jafc.2c03134","article-title":"Novel fluorinated aniline anthranilic diamides improved insecticidal activity targeting the ryanodine receptor","volume":"70","author":"Ren JZ","year":"2022","journal-title":"J Agric Food Chem"},{"key":"e_1_2_8_24_1","doi-asserted-by":"crossref","DOI":"10.1016\/j.bmcl.2020.127535","article-title":"Synthesis, biological activities, and SAR studies of novel 1\u2010(2\u2010chloro\u20104,5\u2010difluorophenyl)\u20101H\u2010pyrazole derivatives","volume":"30","author":"Zhao YY","year":"2022","journal-title":"Bioorg Med Chem Lett"},{"key":"e_1_2_8_25_1","doi-asserted-by":"crossref","first-page":"15665","DOI":"10.1021\/acs.jafc.2c05738","article-title":"3D\u2010QSAR directed discovery of novel halogenated phenyl 3\u2010trifluoroethoxypyrazole containing ultrahigh active insecticidal anthranilic diamides","volume":"70","author":"Yu ZW","year":"2022","journal-title":"J Agric Food Chem"},{"key":"e_1_2_8_26_1","doi-asserted-by":"crossref","first-page":"455","DOI":"10.1002\/jcc.21334","article-title":"AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading","volume":"31","author":"Trott O","year":"2010","journal-title":"J Comput Chem"},{"key":"e_1_2_8_27_1","doi-asserted-by":"crossref","first-page":"265","DOI":"10.1093\/jee\/18.2.265a","article-title":"A method of computing the effectiveness of an insecticide","volume":"18","author":"Abbott WS","year":"1925","journal-title":"J Econ Entomol"},{"key":"e_1_2_8_28_1","doi-asserted-by":"crossref","first-page":"8072","DOI":"10.1021\/acs.jafc.3c08759","article-title":"Discovery of trisubstituted N\u2010phenylpyrazole containing diamides with improved insecticidal activity","volume":"72","author":"Ren JZ","year":"2024","journal-title":"J Agric Food Chem"},{"key":"e_1_2_8_29_1","doi-asserted-by":"crossref","first-page":"16651","DOI":"10.1021\/acs.jafc.4c03361","article-title":"Chlorantraniliprole resistance in spodoptera frugiperda: resistance monitoring, resistance risk, and resistance mechanisms","volume":"72","author":"Guo ZM","year":"2024","journal-title":"J Agric Food Chem"},{"key":"e_1_2_8_30_1","first-page":"90","article-title":"Response of detoxification and immune genes and of transcriptome expression in Mythimna separata following chlorantraniliprole exposure","volume":"28","author":"Wang JD","year":"2018","journal-title":"Comp Biochem Physiol D: Genomics Proteomics"},{"key":"e_1_2_8_31_1","doi-asserted-by":"crossref","first-page":"20653","DOI":"10.1021\/acs.jafc.5c01306","article-title":"Design, synthesis, and evaluation of novel isoxazoline derivatives as potent GABA receptor modulators","volume":"73","author":"Chen Y","year":"2025","journal-title":"J Agric Food Chem"},{"key":"e_1_2_8_32_1","doi-asserted-by":"crossref","first-page":"6385","DOI":"10.1002\/ps.8979","article-title":"Novel boron\u2010containing anthranilic diamide derivatives: design, synthesis, and exploration of the action mode against lepidopteran insects","volume":"81","author":"Xie WB","year":"2025","journal-title":"Pest Manag Sci"},{"key":"e_1_2_8_33_1","doi-asserted-by":"crossref","first-page":"W450","DOI":"10.1093\/nar\/gkae446","article-title":"ChemFREE: a one\u2010stop comprehensive platform for ecological and environmental risk evaluation of chemicals in one health world","volume":"52","author":"Chen DY","year":"2024","journal-title":"Nucleic Acids Res"},{"key":"e_1_2_8_34_1","doi-asserted-by":"crossref","first-page":"W432","DOI":"10.1093\/nar\/gkae298","article-title":"AdmetSAR3.0: a comprehensive platform for exploration, prediction and optimization of chemical ADMET properties","volume":"52","author":"Gu YX","year":"2024","journal-title":"Nucleic Acids Res"}],"container-title":["Pest Management Science"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/scijournals.onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ps.71351","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/scijournals.onlinelibrary.wiley.com\/doi\/full-xml\/10.1002\/ps.71351","content-type":"application\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/scijournals.onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ps.71351","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,10,14]],"date-time":"2026-10-14T07:45:01Z","timestamp":1791963901000},"score":1,"resource":{"primary":{"URL":"https:\/\/scijournals.onlinelibrary.wiley.com\/doi\/10.1002\/ps.71351"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,10,14]]},"references-count":33,"alternative-id":["10.1002\/ps.71351"],"URL":"https:\/\/doi.org\/10.1002\/ps.71351","archive":["Portico"],"relation":{},"ISSN":["1526-498X","1526-4998"],"issn-type":[{"value":"1526-498X","type":"print"},{"value":"1526-4998","type":"electronic"}],"subject":[],"published":{"date-parts":[[2026,10,14]]},"assertion":[{"value":"2026-05-25","order":0,"name":"received","label":"Received","group":{"name":"publication_history","label":"Publication History"}},{"value":"2026-09-11","order":2,"name":"accepted","label":"Accepted","group":{"name":"publication_history","label":"Publication History"}},{"value":"2026-10-14","order":3,"name":"published","label":"Published","group":{"name":"publication_history","label":"Publication History"}}],"article-number":"ps.71351"}}