Antiprotozoal 6-substituted-5,6-dihydro-alpha-pyrones from Raimondia cf. monoica.

ABSTRACT: Dichloromethane extracts of both the roots and the leaves of Raimondia cf. monoica showed in vitro antiplasmodial and leishmanicidal activities against Plasmodium falciparum and Leishmania panamensis, respectively. Three 6-substituted 5,6-dihydro-2H-pyran-2-ones were isolated. (1) and (2)...

Full description

Autores:
Carmona Pedraza, Doris
Sáez Vega, Jairo Antonio
Granados Niño, Hillmer
Pérez Hernández, Edwin Gregorio
Blair Trujillo, Silvia
Angulo Soto, Alberto
Figadere, Bruno
Tipo de recurso:
Article of investigation
Fecha de publicación:
2003
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/37256
Acceso en línea:
https://hdl.handle.net/10495/37256
Palabra clave:
Annonaceae
Antiprotozoarios
Antiprotozoal Agents
Lactonas
Lactones
Leishmania
Estructura Molecular
Molecular Structure
Hojas de la Planta
Plant Leaves
Raíces de Plantas
Plant Roots
Plasmodium falciparum
Pironas
Pyrones
Malaria
Rights
openAccess
License
http://creativecommons.org/licenses/by-nc/2.5/co/
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repository_id_str
dc.title.spa.fl_str_mv Antiprotozoal 6-substituted-5,6-dihydro-alpha-pyrones from Raimondia cf. monoica.
title Antiprotozoal 6-substituted-5,6-dihydro-alpha-pyrones from Raimondia cf. monoica.
spellingShingle Antiprotozoal 6-substituted-5,6-dihydro-alpha-pyrones from Raimondia cf. monoica.
Annonaceae
Antiprotozoarios
Antiprotozoal Agents
Lactonas
Lactones
Leishmania
Estructura Molecular
Molecular Structure
Hojas de la Planta
Plant Leaves
Raíces de Plantas
Plant Roots
Plasmodium falciparum
Pironas
Pyrones
Malaria
title_short Antiprotozoal 6-substituted-5,6-dihydro-alpha-pyrones from Raimondia cf. monoica.
title_full Antiprotozoal 6-substituted-5,6-dihydro-alpha-pyrones from Raimondia cf. monoica.
title_fullStr Antiprotozoal 6-substituted-5,6-dihydro-alpha-pyrones from Raimondia cf. monoica.
title_full_unstemmed Antiprotozoal 6-substituted-5,6-dihydro-alpha-pyrones from Raimondia cf. monoica.
title_sort Antiprotozoal 6-substituted-5,6-dihydro-alpha-pyrones from Raimondia cf. monoica.
dc.creator.fl_str_mv Carmona Pedraza, Doris
Sáez Vega, Jairo Antonio
Granados Niño, Hillmer
Pérez Hernández, Edwin Gregorio
Blair Trujillo, Silvia
Angulo Soto, Alberto
Figadere, Bruno
dc.contributor.author.none.fl_str_mv Carmona Pedraza, Doris
Sáez Vega, Jairo Antonio
Granados Niño, Hillmer
Pérez Hernández, Edwin Gregorio
Blair Trujillo, Silvia
Angulo Soto, Alberto
Figadere, Bruno
dc.contributor.researchgroup.spa.fl_str_mv Grupo Malaria
Química de Plantas Colombianas
dc.subject.decs.none.fl_str_mv Annonaceae
Antiprotozoarios
Antiprotozoal Agents
Lactonas
Lactones
Leishmania
Estructura Molecular
Molecular Structure
Hojas de la Planta
Plant Leaves
Raíces de Plantas
Plant Roots
Plasmodium falciparum
Pironas
Pyrones
Malaria
topic Annonaceae
Antiprotozoarios
Antiprotozoal Agents
Lactonas
Lactones
Leishmania
Estructura Molecular
Molecular Structure
Hojas de la Planta
Plant Leaves
Raíces de Plantas
Plant Roots
Plasmodium falciparum
Pironas
Pyrones
Malaria
description ABSTRACT: Dichloromethane extracts of both the roots and the leaves of Raimondia cf. monoica showed in vitro antiplasmodial and leishmanicidal activities against Plasmodium falciparum and Leishmania panamensis, respectively. Three 6-substituted 5,6-dihydro-2H-pyran-2-ones were isolated. (1) and (2) were identified as (6S)-(5′-oxohepten-1′E,3′E-dienyl)-5,6-dihydro-2H-pyran-2-one (1) and (6R)-(5′-oxohepten-1′Z,3′E-dienyl)-5,6-dihydro-2H-pyran-2-one (2), respectively. (-)-Argentilactone (3) was also isolated. The structure of the new compound (1) was determined by spectroscopic methods; additional spectroscopic data for (2) are reported for the first time
publishDate 2003
dc.date.issued.none.fl_str_mv 2003
dc.date.accessioned.none.fl_str_mv 2023-11-11T19:45:02Z
dc.date.available.none.fl_str_mv 2023-11-11T19:45:02Z
dc.type.spa.fl_str_mv Artículo de investigación
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
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dc.identifier.citation.spa.fl_str_mv Carmona D, Sáez J, Granados H, Pérez E, Blair S, Angulo A, Figadere B. Antiprotozoal 6-substituted-5,6-dihydro-alpha-pyrones from Raimondia cf. monoica. Nat Prod Res. 2003 Aug;17(4):275-80. doi: 10.1080/1057563031000065062.
dc.identifier.issn.none.fl_str_mv 1478-6419
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/37256
dc.identifier.doi.none.fl_str_mv 10.1080/1057563031000065062
dc.identifier.eissn.none.fl_str_mv 1478-6427
identifier_str_mv Carmona D, Sáez J, Granados H, Pérez E, Blair S, Angulo A, Figadere B. Antiprotozoal 6-substituted-5,6-dihydro-alpha-pyrones from Raimondia cf. monoica. Nat Prod Res. 2003 Aug;17(4):275-80. doi: 10.1080/1057563031000065062.
1478-6419
10.1080/1057563031000065062
1478-6427
url https://hdl.handle.net/10495/37256
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Nat. Prod. Res.
dc.relation.citationendpage.spa.fl_str_mv 280
dc.relation.citationissue.spa.fl_str_mv 4
dc.relation.citationstartpage.spa.fl_str_mv 274
dc.relation.citationvolume.spa.fl_str_mv 17
dc.relation.ispartofjournal.spa.fl_str_mv Natural Product Research
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dc.publisher.spa.fl_str_mv Taylor and Francis
dc.publisher.place.spa.fl_str_mv Abingdon, Reino Unido
institution Universidad de Antioquia
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spelling Carmona Pedraza, DorisSáez Vega, Jairo AntonioGranados Niño, HillmerPérez Hernández, Edwin GregorioBlair Trujillo, SilviaAngulo Soto, AlbertoFigadere, BrunoGrupo MalariaQuímica de Plantas Colombianas2023-11-11T19:45:02Z2023-11-11T19:45:02Z2003Carmona D, Sáez J, Granados H, Pérez E, Blair S, Angulo A, Figadere B. Antiprotozoal 6-substituted-5,6-dihydro-alpha-pyrones from Raimondia cf. monoica. Nat Prod Res. 2003 Aug;17(4):275-80. doi: 10.1080/1057563031000065062.1478-6419https://hdl.handle.net/10495/3725610.1080/10575630310000650621478-6427ABSTRACT: Dichloromethane extracts of both the roots and the leaves of Raimondia cf. monoica showed in vitro antiplasmodial and leishmanicidal activities against Plasmodium falciparum and Leishmania panamensis, respectively. Three 6-substituted 5,6-dihydro-2H-pyran-2-ones were isolated. (1) and (2) were identified as (6S)-(5′-oxohepten-1′E,3′E-dienyl)-5,6-dihydro-2H-pyran-2-one (1) and (6R)-(5′-oxohepten-1′Z,3′E-dienyl)-5,6-dihydro-2H-pyran-2-one (2), respectively. (-)-Argentilactone (3) was also isolated. The structure of the new compound (1) was determined by spectroscopic methods; additional spectroscopic data for (2) are reported for the first timeUniversidad de Antioquia. Vicerrectoría de investigación. 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