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New Analogues of (E)-β-Farnesene with Insecticidal Activity and Binding Affinity to Aphid Odorant-Binding Proteins
(E)-β-Farnesene is a strong and efficient alarm pheromone in most aphid species. However, applications in agriculture are prevented by its relatively high volatility, its susceptibility to oxidation and its complex and expensive synthesis. To develop novel compounds for aphid control, we have design...
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Published in: | Journal of agricultural and food chemistry 2011-03, Vol.59 (6), p.2456-2461 |
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container_end_page | 2461 |
container_issue | 6 |
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container_title | Journal of agricultural and food chemistry |
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creator | Sun, Yufeng Qiao, Huili Ling, Yun Yang, Shaoxiang Rui, Changhui Pelosi, Paolo Yang, Xinling |
description | (E)-β-Farnesene is a strong and efficient alarm pheromone in most aphid species. However, applications in agriculture are prevented by its relatively high volatility, its susceptibility to oxidation and its complex and expensive synthesis. To develop novel compounds for aphid control, we have designed and synthesized analogues of (E)-β-farnesene, containing a pyrazole moiety present in several insecticides. Their structures have been confirmed by 1H NMR, elemental analysis, high-resolution mass spectroscopy and IR. Binding activities to three odorant-binding proteins (OBPs) of the pea aphid Acythosiphon pisum have been evaluated and correlated with their structures with reference to (E)-β-farnesene. Several derivatives were shown both to bind to A. pisum OBPs with a specificity similar to that of (E)-β-farnesene and to have aphicidal activity comparable to that of thiacloprid, a commercial insecticide. The compounds synthesized in this work represent new potential agents for aphid population control and provide guidelines to design analogues of (E)-β-farnesene endowed with both insecticidal and repellent activity for aphids. |
doi_str_mv | 10.1021/jf104712c |
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However, applications in agriculture are prevented by its relatively high volatility, its susceptibility to oxidation and its complex and expensive synthesis. To develop novel compounds for aphid control, we have designed and synthesized analogues of (E)-β-farnesene, containing a pyrazole moiety present in several insecticides. Their structures have been confirmed by 1H NMR, elemental analysis, high-resolution mass spectroscopy and IR. Binding activities to three odorant-binding proteins (OBPs) of the pea aphid Acythosiphon pisum have been evaluated and correlated with their structures with reference to (E)-β-farnesene. Several derivatives were shown both to bind to A. pisum OBPs with a specificity similar to that of (E)-β-farnesene and to have aphicidal activity comparable to that of thiacloprid, a commercial insecticide. The compounds synthesized in this work represent new potential agents for aphid population control and provide guidelines to design analogues of (E)-β-farnesene endowed with both insecticidal and repellent activity for aphids.</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/jf104712c</identifier><identifier>PMID: 21341697</identifier><identifier>CODEN: JAFCAU</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Acyrthosiphon pisum ; alarm pheromones ; Animals ; Aphids - chemistry ; Aphids - drug effects ; binding capacity ; Biological and medical sciences ; Crop and Animal Protection Chemistry ; Food industries ; Fundamental and applied biological sciences. Psychology ; infrared spectroscopy ; Insect Proteins - chemistry ; insecticidal properties ; insecticides ; Insecticides - chemical synthesis ; Insecticides - chemistry ; Insecticides - pharmacology ; mass spectrometry ; nuclear magnetic resonance spectroscopy ; oxidation ; Protein Binding ; proteins ; Receptors, Odorant - chemistry ; Sesquiterpenes - chemical synthesis ; Sesquiterpenes - chemistry ; Sesquiterpenes - pharmacology ; Structure-Activity Relationship</subject><ispartof>Journal of agricultural and food chemistry, 2011-03, Vol.59 (6), p.2456-2461</ispartof><rights>Copyright © 2011 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a368t-98c69ac1e6ac62315af1fab69e4aca384bda602dd917fa73e07349c74c0565503</citedby><cites>FETCH-LOGICAL-a368t-98c69ac1e6ac62315af1fab69e4aca384bda602dd917fa73e07349c74c0565503</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24014073$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21341697$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sun, Yufeng</creatorcontrib><creatorcontrib>Qiao, Huili</creatorcontrib><creatorcontrib>Ling, Yun</creatorcontrib><creatorcontrib>Yang, Shaoxiang</creatorcontrib><creatorcontrib>Rui, Changhui</creatorcontrib><creatorcontrib>Pelosi, Paolo</creatorcontrib><creatorcontrib>Yang, Xinling</creatorcontrib><title>New Analogues of (E)-β-Farnesene with Insecticidal Activity and Binding Affinity to Aphid Odorant-Binding Proteins</title><title>Journal of agricultural and food chemistry</title><addtitle>J. Agric. Food Chem</addtitle><description>(E)-β-Farnesene is a strong and efficient alarm pheromone in most aphid species. However, applications in agriculture are prevented by its relatively high volatility, its susceptibility to oxidation and its complex and expensive synthesis. To develop novel compounds for aphid control, we have designed and synthesized analogues of (E)-β-farnesene, containing a pyrazole moiety present in several insecticides. Their structures have been confirmed by 1H NMR, elemental analysis, high-resolution mass spectroscopy and IR. Binding activities to three odorant-binding proteins (OBPs) of the pea aphid Acythosiphon pisum have been evaluated and correlated with their structures with reference to (E)-β-farnesene. Several derivatives were shown both to bind to A. pisum OBPs with a specificity similar to that of (E)-β-farnesene and to have aphicidal activity comparable to that of thiacloprid, a commercial insecticide. The compounds synthesized in this work represent new potential agents for aphid population control and provide guidelines to design analogues of (E)-β-farnesene endowed with both insecticidal and repellent activity for aphids.</description><subject>Acyrthosiphon pisum</subject><subject>alarm pheromones</subject><subject>Animals</subject><subject>Aphids - chemistry</subject><subject>Aphids - drug effects</subject><subject>binding capacity</subject><subject>Biological and medical sciences</subject><subject>Crop and Animal Protection Chemistry</subject><subject>Food industries</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>infrared spectroscopy</subject><subject>Insect Proteins - chemistry</subject><subject>insecticidal properties</subject><subject>insecticides</subject><subject>Insecticides - chemical synthesis</subject><subject>Insecticides - chemistry</subject><subject>Insecticides - pharmacology</subject><subject>mass spectrometry</subject><subject>nuclear magnetic resonance spectroscopy</subject><subject>oxidation</subject><subject>Protein Binding</subject><subject>proteins</subject><subject>Receptors, Odorant - chemistry</subject><subject>Sesquiterpenes - chemical synthesis</subject><subject>Sesquiterpenes - chemistry</subject><subject>Sesquiterpenes - pharmacology</subject><subject>Structure-Activity Relationship</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNpt0c1uEzEQB3ALgWgoHHgB8AVBDwue9cfuHrdVC5UqigQ9ryb-SB1t7GBvWvW1eBCeCUdJSw892fL8NJr5m5C3wD4Dq-HL0gETDdT6GZmBrFklAdrnZMZKsWqlggPyKuclY6yVDXtJDmrgAlTXzEj-bm9pH3CMi43NNDr66fSo-vunOsMUbLbB0ls_XdPzkK2evPYGR9qX242f7igGQ499MD4saO-cD9vHKdJ-fe0NvTQxYZiqe_Ejxcn6kF-TFw7HbN_sz0NydXb66-RbdXH59fykv6iQq3aqularDjVYhVrVHCQ6cDhXnRWokbdiblCx2pgOGocNt6zhotON0EwqKRk_JB93fdcp_i7bTcPKZ23HEYONmzyUMEQLgndFHu2kTjHnZN2wTn6F6W4ANmwjHh4iLvbdvutmvrLmQd5nWsCHPcCscXQlA-3zfycYiDJqce93zmEccJGKufpZb4uMdZLzR51Q52EZN6n8U35ipH-sPpiq</recordid><startdate>20110323</startdate><enddate>20110323</enddate><creator>Sun, Yufeng</creator><creator>Qiao, Huili</creator><creator>Ling, Yun</creator><creator>Yang, Shaoxiang</creator><creator>Rui, Changhui</creator><creator>Pelosi, Paolo</creator><creator>Yang, Xinling</creator><general>American Chemical Society</general><scope>FBQ</scope><scope>IQODW</scope><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></search><sort><creationdate>20110323</creationdate><title>New Analogues of (E)-β-Farnesene with Insecticidal Activity and Binding Affinity to Aphid Odorant-Binding Proteins</title><author>Sun, Yufeng ; Qiao, Huili ; Ling, Yun ; Yang, Shaoxiang ; Rui, Changhui ; Pelosi, Paolo ; Yang, Xinling</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a368t-98c69ac1e6ac62315af1fab69e4aca384bda602dd917fa73e07349c74c0565503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Acyrthosiphon pisum</topic><topic>alarm pheromones</topic><topic>Animals</topic><topic>Aphids - chemistry</topic><topic>Aphids - drug effects</topic><topic>binding capacity</topic><topic>Biological and medical sciences</topic><topic>Crop and Animal Protection Chemistry</topic><topic>Food industries</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>infrared spectroscopy</topic><topic>Insect Proteins - chemistry</topic><topic>insecticidal properties</topic><topic>insecticides</topic><topic>Insecticides - chemical synthesis</topic><topic>Insecticides - chemistry</topic><topic>Insecticides - pharmacology</topic><topic>mass spectrometry</topic><topic>nuclear magnetic resonance spectroscopy</topic><topic>oxidation</topic><topic>Protein Binding</topic><topic>proteins</topic><topic>Receptors, Odorant - chemistry</topic><topic>Sesquiterpenes - chemical synthesis</topic><topic>Sesquiterpenes - chemistry</topic><topic>Sesquiterpenes - pharmacology</topic><topic>Structure-Activity Relationship</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sun, Yufeng</creatorcontrib><creatorcontrib>Qiao, Huili</creatorcontrib><creatorcontrib>Ling, Yun</creatorcontrib><creatorcontrib>Yang, Shaoxiang</creatorcontrib><creatorcontrib>Rui, Changhui</creatorcontrib><creatorcontrib>Pelosi, Paolo</creatorcontrib><creatorcontrib>Yang, Xinling</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><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>Sun, Yufeng</au><au>Qiao, Huili</au><au>Ling, Yun</au><au>Yang, Shaoxiang</au><au>Rui, Changhui</au><au>Pelosi, Paolo</au><au>Yang, Xinling</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New Analogues of (E)-β-Farnesene with Insecticidal Activity and Binding Affinity to Aphid Odorant-Binding Proteins</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2011-03-23</date><risdate>2011</risdate><volume>59</volume><issue>6</issue><spage>2456</spage><epage>2461</epage><pages>2456-2461</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><abstract>(E)-β-Farnesene is a strong and efficient alarm pheromone in most aphid species. However, applications in agriculture are prevented by its relatively high volatility, its susceptibility to oxidation and its complex and expensive synthesis. To develop novel compounds for aphid control, we have designed and synthesized analogues of (E)-β-farnesene, containing a pyrazole moiety present in several insecticides. Their structures have been confirmed by 1H NMR, elemental analysis, high-resolution mass spectroscopy and IR. Binding activities to three odorant-binding proteins (OBPs) of the pea aphid Acythosiphon pisum have been evaluated and correlated with their structures with reference to (E)-β-farnesene. Several derivatives were shown both to bind to A. pisum OBPs with a specificity similar to that of (E)-β-farnesene and to have aphicidal activity comparable to that of thiacloprid, a commercial insecticide. The compounds synthesized in this work represent new potential agents for aphid population control and provide guidelines to design analogues of (E)-β-farnesene endowed with both insecticidal and repellent activity for aphids.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>21341697</pmid><doi>10.1021/jf104712c</doi><tpages>6</tpages></addata></record> |
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subjects | Acyrthosiphon pisum alarm pheromones Animals Aphids - chemistry Aphids - drug effects binding capacity Biological and medical sciences Crop and Animal Protection Chemistry Food industries Fundamental and applied biological sciences. Psychology infrared spectroscopy Insect Proteins - chemistry insecticidal properties insecticides Insecticides - chemical synthesis Insecticides - chemistry Insecticides - pharmacology mass spectrometry nuclear magnetic resonance spectroscopy oxidation Protein Binding proteins Receptors, Odorant - chemistry Sesquiterpenes - chemical synthesis Sesquiterpenes - chemistry Sesquiterpenes - pharmacology Structure-Activity Relationship |
title | New Analogues of (E)-β-Farnesene with Insecticidal Activity and Binding Affinity to Aphid Odorant-Binding Proteins |
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