Aviso: para depositar documentos, por favor, inicia sesión e identifícate con tu cuenta de correo institucional de la UCM con el botón MI CUENTA UCM. No emplees la opción AUTENTICACIÓN CON CONTRASEÑA
 

Germacrone Derivatives as new Insecticidal and Acaricidal Compounds: A Structure-Activity Relationship

dc.contributor.authorGalisteo Pretel, Alberto
dc.contributor.authorPérez del Pulgar, Helena
dc.contributor.authorGuerrero de León, Estela
dc.contributor.authorLópez-Pérez, José Luis
dc.contributor.authorOlmeda García, Ángeles Sonia
dc.contributor.authorGonzalez-Coloma, Azucena
dc.contributor.authorBarrero, Alejandro
dc.contributor.authorQuílez del Moral, José Francisco
dc.date.accessioned2023-06-17T12:34:26Z
dc.date.available2023-06-17T12:34:26Z
dc.date.issued2019
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.
dc.description.departmentDepto. de Sanidad Animal
dc.description.facultyFac. de Veterinaria
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Economía y Competitividad (MINECO)/FEDER
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/65103
dc.identifier.doi10.3390/molecules24162898
dc.identifier.issn1420-3049
dc.identifier.officialurlhttps://doi.org/10.3390/molecules24162898
dc.identifier.relatedurlhttps://www.mdpi.com/1420-3049/24/16/2898
dc.identifier.urihttps://hdl.handle.net/20.500.14352/12528
dc.issue.number16
dc.journal.titleMolecules
dc.language.isoeng
dc.page.initial2898
dc.publisherMDPI
dc.relation.projectIDCTQ-2015-64049-C3-3-R/CTQ2015-64049-C3-1-R
dc.rightsAtribución 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/es/
dc.subject.keywordnatural products
dc.subject.keywordorganic synthesis
dc.subject.keywordbioactive compounds
dc.subject.keywordinsecticidal
dc.subject.keywordixodicidal
dc.subject.ucmAgricultura
dc.titleGermacrone Derivatives as new Insecticidal and Acaricidal Compounds: A Structure-Activity Relationship
dc.typejournal article
dc.volume.number24
dspace.entity.typePublication
relation.isAuthorOfPublication84902757-399b-4951-8e24-546a901d01ec
relation.isAuthorOfPublication.latestForDiscovery84902757-399b-4951-8e24-546a901d01ec

Download

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
molecules-24-02898.pdf
Size:
2.96 MB
Format:
Adobe Portable Document Format

Collections