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)...
- 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/
| id |
UDEA2_c45e868360466956be750c0ddcb059c2 |
|---|---|
| oai_identifier_str |
oai:bibliotecadigital.udea.edu.co:10495/37256 |
| network_acronym_str |
UDEA2 |
| network_name_str |
Repositorio UdeA |
| 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 |
| dc.type.redcol.spa.fl_str_mv |
https://purl.org/redcol/resource_type/ART |
| dc.type.coarversion.spa.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
| dc.type.driver.spa.fl_str_mv |
info:eu-repo/semantics/article |
| dc.type.version.spa.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
| format |
http://purl.org/coar/resource_type/c_2df8fbb1 |
| status_str |
publishedVersion |
| 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 |
| dc.rights.uri.*.fl_str_mv |
http://creativecommons.org/licenses/by-nc/2.5/co/ |
| dc.rights.uri.spa.fl_str_mv |
https://creativecommons.org/licenses/by-nc/4.0/ |
| dc.rights.accessrights.spa.fl_str_mv |
info:eu-repo/semantics/openAccess |
| dc.rights.coar.spa.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
| rights_invalid_str_mv |
http://creativecommons.org/licenses/by-nc/2.5/co/ https://creativecommons.org/licenses/by-nc/4.0/ http://purl.org/coar/access_right/c_abf2 |
| eu_rights_str_mv |
openAccess |
| dc.format.extent.spa.fl_str_mv |
7 |
| dc.format.mimetype.spa.fl_str_mv |
application/pdf |
| dc.publisher.spa.fl_str_mv |
Taylor and Francis |
| dc.publisher.place.spa.fl_str_mv |
Abingdon, Reino Unido |
| institution |
Universidad de Antioquia |
| bitstream.url.fl_str_mv |
https://bibliotecadigital.udea.edu.co/bitstreams/980ecdbb-28d8-481d-bbad-7d12c1d4e565/download https://bibliotecadigital.udea.edu.co/bitstreams/d23a459e-3048-4694-b46c-c55584f2339c/download https://bibliotecadigital.udea.edu.co/bitstreams/4abef66f-2a72-45b1-903d-b90f37510280/download https://bibliotecadigital.udea.edu.co/bitstreams/118bb288-417f-4437-9630-86f4603561e8/download https://bibliotecadigital.udea.edu.co/bitstreams/d0a98309-e297-4812-9b6c-22cae76cdd4a/download |
| bitstream.checksum.fl_str_mv |
c0c92b0ffc8b7d22d9cf56754a416a76 8a4605be74aa9ea9d79846c1fba20a33 240a96988dbc5ef2a17fbe90052ab5cb a30e914d11eb654bf0799f8b9e8e1f81 c83fd4e37bc8489556eed3de29e835cb |
| bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 MD5 MD5 |
| repository.name.fl_str_mv |
Repositorio Institucional de la Universidad de Antioquia |
| repository.mail.fl_str_mv |
aplicacionbibliotecadigitalbiblioteca@udea.edu.co |
| _version_ |
1851052428308250624 |
| 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. Comité para el Desarrollo de la Investigación - CODICOL0007524COL00153297application/pdfengTaylor and FrancisAbingdon, Reino Unidohttp://creativecommons.org/licenses/by-nc/2.5/co/https://creativecommons.org/licenses/by-nc/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Antiprotozoal 6-substituted-5,6-dihydro-alpha-pyrones from Raimondia cf. monoica.Artículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionAnnonaceaeAntiprotozoariosAntiprotozoal AgentsLactonasLactonesLeishmaniaEstructura MolecularMolecular StructureHojas de la PlantaPlant LeavesRaíces de PlantasPlant RootsPlasmodium falciparumPironasPyronesMalariaNat. Prod. Res.280427417Natural Product ResearchRoR:03bp5hc83PublicationCC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8933https://bibliotecadigital.udea.edu.co/bitstreams/980ecdbb-28d8-481d-bbad-7d12c1d4e565/downloadc0c92b0ffc8b7d22d9cf56754a416a76MD52falseAnonymousREADLICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://bibliotecadigital.udea.edu.co/bitstreams/d23a459e-3048-4694-b46c-c55584f2339c/download8a4605be74aa9ea9d79846c1fba20a33MD53falseAnonymousREADORIGINALCarmonaDoris_2010_AntiprotozoalRaimondiaCFMonoica.pdfCarmonaDoris_2010_AntiprotozoalRaimondiaCFMonoica.pdfArtículo de investigaciónapplication/pdf302279https://bibliotecadigital.udea.edu.co/bitstreams/4abef66f-2a72-45b1-903d-b90f37510280/download240a96988dbc5ef2a17fbe90052ab5cbMD51trueAnonymousREADTEXTCarmonaDoris_2010_AntiprotozoalRaimondiaCFMonoica.pdf.txtCarmonaDoris_2010_AntiprotozoalRaimondiaCFMonoica.pdf.txtExtracted texttext/plain18176https://bibliotecadigital.udea.edu.co/bitstreams/118bb288-417f-4437-9630-86f4603561e8/downloada30e914d11eb654bf0799f8b9e8e1f81MD54falseAnonymousREADTHUMBNAILCarmonaDoris_2010_AntiprotozoalRaimondiaCFMonoica.pdf.jpgCarmonaDoris_2010_AntiprotozoalRaimondiaCFMonoica.pdf.jpgGenerated Thumbnailimage/jpeg9660https://bibliotecadigital.udea.edu.co/bitstreams/d0a98309-e297-4812-9b6c-22cae76cdd4a/downloadc83fd4e37bc8489556eed3de29e835cbMD55falseAnonymousREAD10495/37256oai:bibliotecadigital.udea.edu.co:10495/372562025-03-26 22:11:51.114http://creativecommons.org/licenses/by-nc/2.5/co/open.accesshttps://bibliotecadigital.udea.edu.coRepositorio Institucional de la Universidad de Antioquiaaplicacionbibliotecadigitalbiblioteca@udea.edu.coTk9URTogUExBQ0UgWU9VUiBPV04gTElDRU5TRSBIRVJFClRoaXMgc2FtcGxlIGxpY2Vuc2UgaXMgcHJvdmlkZWQgZm9yIGluZm9ybWF0aW9uYWwgcHVycG9zZXMgb25seS4KCk5PTi1FWENMVVNJVkUgRElTVFJJQlVUSU9OIExJQ0VOU0UKCkJ5IHNpZ25pbmcgYW5kIHN1Ym1pdHRpbmcgdGhpcyBsaWNlbnNlLCB5b3UgKHRoZSBhdXRob3Iocykgb3IgY29weXJpZ2h0Cm93bmVyKSBncmFudHMgdG8gRFNwYWNlIFVuaXZlcnNpdHkgKERTVSkgdGhlIG5vbi1leGNsdXNpdmUgcmlnaHQgdG8gcmVwcm9kdWNlLAp0cmFuc2xhdGUgKGFzIGRlZmluZWQgYmVsb3cpLCBhbmQvb3IgZGlzdHJpYnV0ZSB5b3VyIHN1Ym1pc3Npb24gKGluY2x1ZGluZwp0aGUgYWJzdHJhY3QpIHdvcmxkd2lkZSBpbiBwcmludCBhbmQgZWxlY3Ryb25pYyBmb3JtYXQgYW5kIGluIGFueSBtZWRpdW0sCmluY2x1ZGluZyBidXQgbm90IGxpbWl0ZWQgdG8gYXVkaW8gb3IgdmlkZW8uCgpZb3UgYWdyZWUgdGhhdCBEU1UgbWF5LCB3aXRob3V0IGNoYW5naW5nIHRoZSBjb250ZW50LCB0cmFuc2xhdGUgdGhlCnN1Ym1pc3Npb24gdG8gYW55IG1lZGl1bSBvciBmb3JtYXQgZm9yIHRoZSBwdXJwb3NlIG9mIHByZXNlcnZhdGlvbi4KCllvdSBhbHNvIGFncmVlIHRoYXQgRFNVIG1heSBrZWVwIG1vcmUgdGhhbiBvbmUgY29weSBvZiB0aGlzIHN1Ym1pc3Npb24gZm9yCnB1cnBvc2VzIG9mIHNlY3VyaXR5LCBiYWNrLXVwIGFuZCBwcmVzZXJ2YXRpb24uCgpZb3UgcmVwcmVzZW50IHRoYXQgdGhlIHN1Ym1pc3Npb24gaXMgeW91ciBvcmlnaW5hbCB3b3JrLCBhbmQgdGhhdCB5b3UgaGF2ZQp0aGUgcmlnaHQgdG8gZ3JhbnQgdGhlIHJpZ2h0cyBjb250YWluZWQgaW4gdGhpcyBsaWNlbnNlLiBZb3UgYWxzbyByZXByZXNlbnQKdGhhdCB5b3VyIHN1Ym1pc3Npb24gZG9lcyBub3QsIHRvIHRoZSBiZXN0IG9mIHlvdXIga25vd2xlZGdlLCBpbmZyaW5nZSB1cG9uCmFueW9uZSdzIGNvcHlyaWdodC4KCklmIHRoZSBzdWJtaXNzaW9uIGNvbnRhaW5zIG1hdGVyaWFsIGZvciB3aGljaCB5b3UgZG8gbm90IGhvbGQgY29weXJpZ2h0LAp5b3UgcmVwcmVzZW50IHRoYXQgeW91IGhhdmUgb2J0YWluZWQgdGhlIHVucmVzdHJpY3RlZCBwZXJtaXNzaW9uIG9mIHRoZQpjb3B5cmlnaHQgb3duZXIgdG8gZ3JhbnQgRFNVIHRoZSByaWdodHMgcmVxdWlyZWQgYnkgdGhpcyBsaWNlbnNlLCBhbmQgdGhhdApzdWNoIHRoaXJkLXBhcnR5IG93bmVkIG1hdGVyaWFsIGlzIGNsZWFybHkgaWRlbnRpZmllZCBhbmQgYWNrbm93bGVkZ2VkCndpdGhpbiB0aGUgdGV4dCBvciBjb250ZW50IG9mIHRoZSBzdWJtaXNzaW9uLgoKSUYgVEhFIFNVQk1JU1NJT04gSVMgQkFTRUQgVVBPTiBXT1JLIFRIQVQgSEFTIEJFRU4gU1BPTlNPUkVEIE9SIFNVUFBPUlRFRApCWSBBTiBBR0VOQ1kgT1IgT1JHQU5JWkFUSU9OIE9USEVSIFRIQU4gRFNVLCBZT1UgUkVQUkVTRU5UIFRIQVQgWU9VIEhBVkUKRlVMRklMTEVEIEFOWSBSSUdIVCBPRiBSRVZJRVcgT1IgT1RIRVIgT0JMSUdBVElPTlMgUkVRVUlSRUQgQlkgU1VDSApDT05UUkFDVCBPUiBBR1JFRU1FTlQuCgpEU1Ugd2lsbCBjbGVhcmx5IGlkZW50aWZ5IHlvdXIgbmFtZShzKSBhcyB0aGUgYXV0aG9yKHMpIG9yIG93bmVyKHMpIG9mIHRoZQpzdWJtaXNzaW9uLCBhbmQgd2lsbCBub3QgbWFrZSBhbnkgYWx0ZXJhdGlvbiwgb3RoZXIgdGhhbiBhcyBhbGxvd2VkIGJ5IHRoaXMKbGljZW5zZSwgdG8geW91ciBzdWJtaXNzaW9uLgo= |
