Constituents of two Flourensia species

Autores
Uriburu, María L.; de la Fuente, Juana Rosa; Palermo, Jorge Alejandro; Gil, Roberto Ricardo; Sosa, Virginia Estela
Año de publicación
2004
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The MeOH extract of aerial parts of Flourensia riparia Grisebach (Asteraceae) afforded a sesquiterpene lactone, 4beta-hydroxy-4,10alpha-dimethyl-7alphaH,8alphaH-eudesman-11-ene-8,12-olide, together with septuplinolide, its isomer at positions C-5 and C-10. In addition, known flavonoids, p-hydroxyacetophenone derivatives, carabrone and isoalantolactone were identified. Three known flavonoids and a benzofuran were isolated from Flourensia campestris Wedd.
Fil: Uriburu, María L.. Universidad Nacional de Salta; Argentina
Fil: de la Fuente, Juana Rosa. Universidad Nacional de Salta; Argentina
Fil: Palermo, Jorge Alejandro. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina
Fil: Gil, Roberto Ricardo. University of Carnegie Mellon; Estados Unidos
Fil: Sosa, Virginia Estela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina
Materia
Flourensia Riparia
Flourensia Campestri
Asteraceae
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/41094
Acceder
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network_name_str CONICET Digital (CONICET)
spelling Constituents of two Flourensia speciesUriburu, María L.de la Fuente, Juana RosaPalermo, Jorge AlejandroGil, Roberto RicardoSosa, Virginia EstelaFlourensia RipariaFlourensia CampestriAsteraceaehttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The MeOH extract of aerial parts of Flourensia riparia Grisebach (Asteraceae) afforded a sesquiterpene lactone, 4beta-hydroxy-4,10alpha-dimethyl-7alphaH,8alphaH-eudesman-11-ene-8,12-olide, together with septuplinolide, its isomer at positions C-5 and C-10. In addition, known flavonoids, p-hydroxyacetophenone derivatives, carabrone and isoalantolactone were identified. Three known flavonoids and a benzofuran were isolated from Flourensia campestris Wedd.Fil: Uriburu, María L.. Universidad Nacional de Salta; ArgentinaFil: de la Fuente, Juana Rosa. Universidad Nacional de Salta; ArgentinaFil: Palermo, Jorge Alejandro. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; ArgentinaFil: Gil, Roberto Ricardo. University of Carnegie Mellon; Estados UnidosFil: Sosa, Virginia Estela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; ArgentinaPergamon-Elsevier Science Ltd2004-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/41094Uriburu, María L.; de la Fuente, Juana Rosa; Palermo, Jorge Alejandro; Gil, Roberto Ricardo; Sosa, Virginia Estela; Constituents of two Flourensia species; Pergamon-Elsevier Science Ltd; Phytochemistry; 65; 14; 7-2004; 2039-20430031-9422CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0031942204002225info:eu-repo/semantics/altIdentifier/doi/10.1016/j.phytochem.2004.05.009info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:19:08Zoai:ri.conicet.gov.ar:11336/41094instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-10 13:19:09.129CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Constituents of two Flourensia species
title Constituents of two Flourensia species
spellingShingle Constituents of two Flourensia species
Uriburu, María L.
Flourensia Riparia
Flourensia Campestri
Asteraceae
title_short Constituents of two Flourensia species
title_full Constituents of two Flourensia species
title_fullStr Constituents of two Flourensia species
title_full_unstemmed Constituents of two Flourensia species
title_sort Constituents of two Flourensia species
dc.creator.none.fl_str_mv Uriburu, María L.
de la Fuente, Juana Rosa
Palermo, Jorge Alejandro
Gil, Roberto Ricardo
Sosa, Virginia Estela
author Uriburu, María L.
author_facet Uriburu, María L.
de la Fuente, Juana Rosa
Palermo, Jorge Alejandro
Gil, Roberto Ricardo
Sosa, Virginia Estela
author_role author
author2 de la Fuente, Juana Rosa
Palermo, Jorge Alejandro
Gil, Roberto Ricardo
Sosa, Virginia Estela
author2_role author
author
author
author
dc.subject.none.fl_str_mv Flourensia Riparia
Flourensia Campestri
Asteraceae
topic Flourensia Riparia
Flourensia Campestri
Asteraceae
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The MeOH extract of aerial parts of Flourensia riparia Grisebach (Asteraceae) afforded a sesquiterpene lactone, 4beta-hydroxy-4,10alpha-dimethyl-7alphaH,8alphaH-eudesman-11-ene-8,12-olide, together with septuplinolide, its isomer at positions C-5 and C-10. In addition, known flavonoids, p-hydroxyacetophenone derivatives, carabrone and isoalantolactone were identified. Three known flavonoids and a benzofuran were isolated from Flourensia campestris Wedd.
Fil: Uriburu, María L.. Universidad Nacional de Salta; Argentina
Fil: de la Fuente, Juana Rosa. Universidad Nacional de Salta; Argentina
Fil: Palermo, Jorge Alejandro. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina
Fil: Gil, Roberto Ricardo. University of Carnegie Mellon; Estados Unidos
Fil: Sosa, Virginia Estela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina
description The MeOH extract of aerial parts of Flourensia riparia Grisebach (Asteraceae) afforded a sesquiterpene lactone, 4beta-hydroxy-4,10alpha-dimethyl-7alphaH,8alphaH-eudesman-11-ene-8,12-olide, together with septuplinolide, its isomer at positions C-5 and C-10. In addition, known flavonoids, p-hydroxyacetophenone derivatives, carabrone and isoalantolactone were identified. Three known flavonoids and a benzofuran were isolated from Flourensia campestris Wedd.
publishDate 2004
dc.date.none.fl_str_mv 2004-07
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/41094
Uriburu, María L.; de la Fuente, Juana Rosa; Palermo, Jorge Alejandro; Gil, Roberto Ricardo; Sosa, Virginia Estela; Constituents of two Flourensia species; Pergamon-Elsevier Science Ltd; Phytochemistry; 65; 14; 7-2004; 2039-2043
0031-9422
CONICET Digital
CONICET
url http://hdl.handle.net/11336/41094
identifier_str_mv Uriburu, María L.; de la Fuente, Juana Rosa; Palermo, Jorge Alejandro; Gil, Roberto Ricardo; Sosa, Virginia Estela; Constituents of two Flourensia species; Pergamon-Elsevier Science Ltd; Phytochemistry; 65; 14; 7-2004; 2039-2043
0031-9422
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0031942204002225
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.phytochem.2004.05.009
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Pergamon-Elsevier Science Ltd
publisher.none.fl_str_mv Pergamon-Elsevier Science Ltd
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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score 12.48226

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