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dc.contributor.authorGalisteo Pretel, Alberto
dc.contributor.authorPérez del Pulgar, Helena
dc.contributor.authorFernández Barrero, Alejandro 
dc.contributor.authorQuílez Del Moral, José Francisco 
dc.date.accessioned2020-04-22T06:34:41Z
dc.date.available2020-04-22T06:34:41Z
dc.date.issued2019-08-09
dc.identifier.citationGalisteo Pretel, A.; Pérez del Pulgar, H.; Guerrero de León, E.; López-Pérez, J.L.; Olmeda, A.S.; Gonzalez-Coloma, A.; F. Barrero, A.; Quílez del Moral, J.F. Germacrone Derivatives as new Insecticidal and Acaricidal Compounds: A Structure-Activity Relationship. Molecules 2019, 24, 2898. [doi:10.3390/molecules24162898]es_ES
dc.identifier.urihttp://hdl.handle.net/10481/61450
dc.descriptionThe supplementary material related to this article includes NMR spectra of new compounds is available online at https://www.mdpi.com/1420-3049/24/16/2898/s1.es_ES
dc.description.abstractCurrently, the use of synthetic pesticides is the main method of plant protection applied in agri- and horticulture. However, its excessive use leads to the development of pesticide resistance, a contamination of the environment, toxicity to non-target organisms, and risks for human health. With the ultimate aim of contributing to the develop of a more sustainable pest management, we used the natural product germacrone (compound 1), reported to possess significant insecticidal activity, as starting material for the generation of molecular diversity (2–24). Some of the generated derivatives are natural compounds, such as 1,10-epoxygermacrone (2), 4,5-epoxygermacrone (3), gajutsulactone A (7), germacrol (11), isogermacrone (14), 9-hydroxyeudesma-3,7(11)dien-6-one (19), eudesma-4,7(11),dien-8-one (20), eudesma-3,7(11)-dien-8-one (21) and eudesma-4(15),7(11)-dien-8-one (22). Compounds, 7,11-9,10-diepoxigermacr-4,5-en-8-ol (17), 7,11-epoxieudesma-4,7(11)-dien-8-one (23) and 7,11-epoxieudesma-3,7(11)-dien-8-one (24) are described for the first time. The biocidal activity of most of these compounds was assayed against the tick Hyalomma lusitanicum. The acaricidal effects of compound 24 were four times higher than that of germacrone (1). Compound 2 is an insect antifeedant a thousand times more potent than germacrone against Rhopalosiphum padi, which makes this substance a promising selective antifeedant against this cereal pest.es_ES
dc.description.sponsorshipThis research was funded by Grant CTQ-2015-64049-C3-3-R/CTQ2015-64049-C3-1-R; MINISTERIO DE ECONOMÍA Y COMPETITIVIDAD, Spain (MINECO/FEDER).es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsAtribución 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectNatural productses_ES
dc.subjectOrganic synthesises_ES
dc.subjectBioactive compoundses_ES
dc.subjectInsecticidales_ES
dc.subjectIxodicidales_ES
dc.titleArticle Germacrone Derivatives as new Insecticidal and Acaricidal Compounds: A Structure-Activity Relationshipes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.doi10.3390/molecules24162898


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Atribución 3.0 España
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