Design, Synthesis, and Insecticidal Activity of Novel Isoxazoline Diacylhydrazine Compounds as GABA Receptor Inhibitors
A series of isoxazoline derivatives containing diacylhydrazine moieties were designed and synthesized as potential insecticides. Most of these derivatives exhibited good insecticidal activities against Plutella xylostella, and some compounds exhibited excellent insecticidal activities against Spodop...
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Veröffentlicht in: | Journal of agricultural and food chemistry 2023-05, Vol.71 (17), p.6561-6569 |
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creator | Li, Yahui Zhang, Wenbo Wu, Zengxue Song, Baoan Song, Runjiang |
description | A series of isoxazoline derivatives containing diacylhydrazine moieties were designed and synthesized as potential insecticides. Most of these derivatives exhibited good insecticidal activities against Plutella xylostella, and some compounds exhibited excellent insecticidal activities against Spodoptera frugiperda. Especially, D14 showed outstanding insecticidal activity against P. xylostella (LC50 = 0.37 μg/mL), which was superior to that of ethiprole (LC50 = 2.84 μg/mL) and tebufenozide (LC50 = 15.3 μg/mL) and similar to that of fluxametamide (LC50 = 0.30 μg/mL). Remarkably, the insecticidal activity of D14 against S. frugiperda (LC50 = 1.72 μg/mL) was superior to that of chlorantraniliprole (LC50 = 3.64 μg/mL) and tebufenozide (LC50 = 60.5 μg/mL) but lower than that of fluxametamide (LC50 = 0.14 μg/mL). The results of electrophysiological experiments, molecular docking, and proteomics experiments indicate that compound D14 acts by interfering with the γ-aminobutyric acid receptor to control pests. |
doi_str_mv | 10.1021/acs.jafc.2c08880 |
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Most of these derivatives exhibited good insecticidal activities against Plutella xylostella, and some compounds exhibited excellent insecticidal activities against Spodoptera frugiperda. Especially, D14 showed outstanding insecticidal activity against P. xylostella (LC50 = 0.37 μg/mL), which was superior to that of ethiprole (LC50 = 2.84 μg/mL) and tebufenozide (LC50 = 15.3 μg/mL) and similar to that of fluxametamide (LC50 = 0.30 μg/mL). Remarkably, the insecticidal activity of D14 against S. frugiperda (LC50 = 1.72 μg/mL) was superior to that of chlorantraniliprole (LC50 = 3.64 μg/mL) and tebufenozide (LC50 = 60.5 μg/mL) but lower than that of fluxametamide (LC50 = 0.14 μg/mL). The results of electrophysiological experiments, molecular docking, and proteomics experiments indicate that compound D14 acts by interfering with the γ-aminobutyric acid receptor to control pests.</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/acs.jafc.2c08880</identifier><identifier>PMID: 37075263</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Agricultural and Environmental Chemistry ; Hydrazines - pharmacology ; Insecticides - pharmacology ; Isoxazoles - chemistry ; Isoxazoles - pharmacology ; Molecular Docking Simulation ; Receptors, GABA</subject><ispartof>Journal of agricultural and food chemistry, 2023-05, Vol.71 (17), p.6561-6569</ispartof><rights>2023 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a336t-94b7e07d41ad2a231e8f70124a70380f96e34176311b35f375d5aa2560a0684f3</citedby><cites>FETCH-LOGICAL-a336t-94b7e07d41ad2a231e8f70124a70380f96e34176311b35f375d5aa2560a0684f3</cites><orcidid>0000-0003-2502-778X ; 0000-0001-5721-4227 ; 0000-0002-1980-1751 ; 0000-0003-3629-7259 ; 0000-0002-4237-6167</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.jafc.2c08880$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.jafc.2c08880$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2763,27074,27922,27923,56736,56786</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37075263$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Yahui</creatorcontrib><creatorcontrib>Zhang, Wenbo</creatorcontrib><creatorcontrib>Wu, Zengxue</creatorcontrib><creatorcontrib>Song, Baoan</creatorcontrib><creatorcontrib>Song, Runjiang</creatorcontrib><title>Design, Synthesis, and Insecticidal Activity of Novel Isoxazoline Diacylhydrazine Compounds as GABA Receptor Inhibitors</title><title>Journal of agricultural and food chemistry</title><addtitle>J. Agric. Food Chem</addtitle><description>A series of isoxazoline derivatives containing diacylhydrazine moieties were designed and synthesized as potential insecticides. Most of these derivatives exhibited good insecticidal activities against Plutella xylostella, and some compounds exhibited excellent insecticidal activities against Spodoptera frugiperda. Especially, D14 showed outstanding insecticidal activity against P. xylostella (LC50 = 0.37 μg/mL), which was superior to that of ethiprole (LC50 = 2.84 μg/mL) and tebufenozide (LC50 = 15.3 μg/mL) and similar to that of fluxametamide (LC50 = 0.30 μg/mL). Remarkably, the insecticidal activity of D14 against S. frugiperda (LC50 = 1.72 μg/mL) was superior to that of chlorantraniliprole (LC50 = 3.64 μg/mL) and tebufenozide (LC50 = 60.5 μg/mL) but lower than that of fluxametamide (LC50 = 0.14 μg/mL). The results of electrophysiological experiments, molecular docking, and proteomics experiments indicate that compound D14 acts by interfering with the γ-aminobutyric acid receptor to control pests.</description><subject>Agricultural and Environmental Chemistry</subject><subject>Hydrazines - pharmacology</subject><subject>Insecticides - pharmacology</subject><subject>Isoxazoles - chemistry</subject><subject>Isoxazoles - pharmacology</subject><subject>Molecular Docking Simulation</subject><subject>Receptors, GABA</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM9P2zAYhq2Jae067pwmH3dous92_KPHrjCohEDaxjn66jjUKI27OAHCXz93Ldw4-bX0vK_0PYScMZgx4Ow72jh7wMrOuAVjDHwgYyY5ZJIxc0LGkJjMSMVG5HOMDwBgpIZPZCQ0aMmVGJOncxf9fTOlv4em26QcpxSbkq6a6GznrS-xpouUHn030FDRm_DoarqK4RlfQu0bR8892qHeDGWLL_v_Mmx3oW_KSDHSy8WPBf3lrNt1oU2rG7_2KcUv5GOFdXSnx3dC7n5e_FleZde3l6vl4jpDIVSXzfO1dqDLnGHJkQvmTKWB8Rw1CAPVXDmRM60EY2shK6FlKRG5VICgTF6JCfl22N214W_vYldsfbSurrFxoY8FNyDmSkklEgoH1LYhxtZVxa71W2yHgkGx110k3cVed3HUnSpfj-v9euvKt8Kr3wRMD8D_aujbJh37_t4_vn2LmA</recordid><startdate>20230503</startdate><enddate>20230503</enddate><creator>Li, Yahui</creator><creator>Zhang, Wenbo</creator><creator>Wu, Zengxue</creator><creator>Song, Baoan</creator><creator>Song, Runjiang</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2502-778X</orcidid><orcidid>https://orcid.org/0000-0001-5721-4227</orcidid><orcidid>https://orcid.org/0000-0002-1980-1751</orcidid><orcidid>https://orcid.org/0000-0003-3629-7259</orcidid><orcidid>https://orcid.org/0000-0002-4237-6167</orcidid></search><sort><creationdate>20230503</creationdate><title>Design, Synthesis, and Insecticidal Activity of Novel Isoxazoline Diacylhydrazine Compounds as GABA Receptor Inhibitors</title><author>Li, Yahui ; Zhang, Wenbo ; Wu, Zengxue ; Song, Baoan ; Song, Runjiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a336t-94b7e07d41ad2a231e8f70124a70380f96e34176311b35f375d5aa2560a0684f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Agricultural and Environmental Chemistry</topic><topic>Hydrazines - pharmacology</topic><topic>Insecticides - pharmacology</topic><topic>Isoxazoles - chemistry</topic><topic>Isoxazoles - pharmacology</topic><topic>Molecular Docking Simulation</topic><topic>Receptors, GABA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Yahui</creatorcontrib><creatorcontrib>Zhang, Wenbo</creatorcontrib><creatorcontrib>Wu, Zengxue</creatorcontrib><creatorcontrib>Song, Baoan</creatorcontrib><creatorcontrib>Song, Runjiang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Yahui</au><au>Zhang, Wenbo</au><au>Wu, Zengxue</au><au>Song, Baoan</au><au>Song, Runjiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Design, Synthesis, and Insecticidal Activity of Novel Isoxazoline Diacylhydrazine Compounds as GABA Receptor Inhibitors</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2023-05-03</date><risdate>2023</risdate><volume>71</volume><issue>17</issue><spage>6561</spage><epage>6569</epage><pages>6561-6569</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><abstract>A series of isoxazoline derivatives containing diacylhydrazine moieties were designed and synthesized as potential insecticides. Most of these derivatives exhibited good insecticidal activities against Plutella xylostella, and some compounds exhibited excellent insecticidal activities against Spodoptera frugiperda. Especially, D14 showed outstanding insecticidal activity against P. xylostella (LC50 = 0.37 μg/mL), which was superior to that of ethiprole (LC50 = 2.84 μg/mL) and tebufenozide (LC50 = 15.3 μg/mL) and similar to that of fluxametamide (LC50 = 0.30 μg/mL). Remarkably, the insecticidal activity of D14 against S. frugiperda (LC50 = 1.72 μg/mL) was superior to that of chlorantraniliprole (LC50 = 3.64 μg/mL) and tebufenozide (LC50 = 60.5 μg/mL) but lower than that of fluxametamide (LC50 = 0.14 μg/mL). The results of electrophysiological experiments, molecular docking, and proteomics experiments indicate that compound D14 acts by interfering with the γ-aminobutyric acid receptor to control pests.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>37075263</pmid><doi>10.1021/acs.jafc.2c08880</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-2502-778X</orcidid><orcidid>https://orcid.org/0000-0001-5721-4227</orcidid><orcidid>https://orcid.org/0000-0002-1980-1751</orcidid><orcidid>https://orcid.org/0000-0003-3629-7259</orcidid><orcidid>https://orcid.org/0000-0002-4237-6167</orcidid></addata></record> |
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subjects | Agricultural and Environmental Chemistry Hydrazines - pharmacology Insecticides - pharmacology Isoxazoles - chemistry Isoxazoles - pharmacology Molecular Docking Simulation Receptors, GABA |
title | Design, Synthesis, and Insecticidal Activity of Novel Isoxazoline Diacylhydrazine Compounds as GABA Receptor Inhibitors |
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