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dc.contributor.authorArgandoña, Víctor H.en_US
dc.contributor.authorRovirosa, Juanaen_US
dc.contributor.authorSan Martín, Aurelioen_US
dc.contributor.authorRiquelme, Alejandroen_US
dc.contributor.authorDíaz-Marrero, Ana R.en_US
dc.contributor.authorCueto, Mercedesen_US
dc.contributor.authorDarias, Joséen_US
dc.contributor.authorSantana, Omaren_US
dc.contributor.authorGuadaño-Ferraz, Anaen_US
dc.contributor.authorGonzález-Coloma, Azucena-
dc.date.accessioned2009-05-28T07:14:51Z-
dc.date.available2009-05-28T07:14:51Z-
dc.date.issued2002-10-22en_US
dc.identifier.citationJournal of Agricultural and Food Chemistry 50(24): 7029-7033 (2002)en_US
dc.identifier.issn0021-8561-
dc.identifier.urihttp://hdl.handle.net/10261/13269-
dc.description5 pages, 3 tables, 1 chart.-- PMID: 12428955 [PubMed].-- Printed version published Nov 20, 2002.-
dc.descriptionSupporting information available: Table showing the phytotoxic effects of compounds 11-13 on barley and tomato leaves.-- Available at: http://pubs.acs.org/doi/suppl/10.1021/jf025857p?cookieSet=1-
dc.description.abstractIn this work the antifeedant effects of the halogenated monoterpenes 1−13 were tested against several divergent insect species. These compounds have been isolated from Plocamium cartilagineum (6 was isolated as an acetyl derivative), except for 4, which was isolated from Pantoneura plocamioides. We have also included the semisynthetic derivatives 1a, 2a, and 7. Compounds 1, 1a, 2, 4, 5, 7, 8−10, and 13 were antifeedants against Leptinotarsa decemlineata with varying potencies. The aphids Myzus persicae and Ropalosiphum padi were strongly deterred in the presence of compounds 2, 12, and 13. This effect was correlated with the electronic recording of their probing behavior. Compounds 2 and 12 were toxic to L. decemlineata and had selective cytotoxicity to insect-derived Sf9 cells. None of the tested compounds showed phytotoxic effects. The antifeedant and cytotoxic effects of these compounds were compared with those of the polyhalogenated insecticide γ-hexachlorocyclohexane (lindane).-
dc.description.sponsorshipA.R.D.-M., M.C., O.S., and A.G. acknowledge I3P-CSIC (predoctoral and postdoctoral), AECI (predoctoral), and MEC/Contrato de Reincorporación Fellowships. This work was partially supported by Convenio CSIC-U.Chile and Grants FONDECYT 1990935, Instituto Antártico Chileno (INACH), MCYT-Spain (BQU2001-1505; PPQ2002-02494), and CYTED IV.13.-
dc.format.extent2373 bytes-
dc.format.extent76511 bytes-
dc.format.mimetypetext/plain-
dc.format.mimetypeapplication/pdf-
dc.language.isoengen_US
dc.publisherAmerican Chemical Society-
dc.rightsclosedAccessen_US
dc.subjectHalogenated monoterpenes-
dc.subjectInsect antifeedants-
dc.titleAntifeedant effects of marine halogenated monoterpenesen_US
dc.typeartículoen_US
dc.identifier.doi10.1021/jf025857p-
dc.relation.publisherversionhttp://dx.doi.org/10.1021/jf025857p-
dc.contributor.funderConsejo Superior de Investigaciones Científicas (España)-
dc.contributor.funderMinisterio de Asuntos Exteriores y Cooperación (España)-
dc.contributor.funderMinisterio de Educación y Ciencia (España)-
dc.contributor.funderInstituto Antártico Chileno-
dc.contributor.funderFondo Nacional de Desarrollo Científico y Tecnológico (Chile)-
dc.contributor.funderMinisterio de Ciencia y Tecnología (España)-
dc.contributor.funderPrograma Iberoamericano de Ciencia y Tecnología para el Desarrollo-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003339es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003767es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100002850es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100006280es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeartículo-
item.cerifentitytypePublications-
item.grantfulltextnone-
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