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dc.contributor.authorCastaño Gil, Yenni Marcela-
dc.contributor.authorCardona Galeano, Wilson-
dc.contributor.authorQuiñones Fletcher, Winston-
dc.contributor.authorRobledo Restrepo, Sara María-
dc.contributor.authorEcheverrí López, Luis Fernando-
dc.date.accessioned2021-11-01T18:45:00Z-
dc.date.available2021-11-01T18:45:00Z-
dc.date.issued2009-
dc.identifier.citationCastaño, M., Cardona, W., Quiñones, W., Robledo, S., & Echeverri, F. (2009). Leishmanicidal Activity of Aliphatic and Aromatic Lactones: Correlation Structure-Activity. Molecules, 14(7), 2491–2500. Retrieved from http://dx.doi.org/10.3390/molecules14072491spa
dc.identifier.urihttp://hdl.handle.net/10495/23676-
dc.description.abstractABSTRACT: Several aliphatic and aromatic lactones and two dimers were synthesized using the sequence: allylation - esterification - metathesis. These compounds were active in vitro against intracellular amastigotes of Leishmania panamensis. The structure-activity relationship showed the importance of the aliphatic side chain to enhance the biological activity and to obtain lower cytotoxicity. It was also observed that a decrease in the size of the lactone ring increases the selectivity index.spa
dc.format.extent10spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherMDPIspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/co/*
dc.titleLeishmanicidal Activity of Aliphatic and Aromatic Lactones : Correlation Structure-Activityspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupPrograma de Estudio y Control de Enfermedades Tropicales (PECET)spa
dc.publisher.groupQuímica de Plantas Colombianasspa
dc.publisher.groupQuímica Orgánica de Productos Naturalesspa
dc.identifier.doi10.3390/molecules14072491-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1420-3049-
oaire.citationtitleMoleculesspa
oaire.citationstartpage2491spa
oaire.citationendpage2500spa
oaire.citationvolume14spa
oaire.citationissue7spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by/4.0/spa
dc.publisher.placeBasilea, Suizaspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsFonética-
dc.subject.decsPhonetics-
dc.subject.decsAntiparasitarios-
dc.subject.decsAntiparasitic Agents-
dc.subject.agrovocLactones-
dc.subject.agrovocLactonas-
dc.subject.agrovocLeishmaniosis-
dc.subject.agrovocLeishmaniosis-
dc.subject.proposalMetátesisspa
dc.subject.agrovocurihttp://aims.fao.org/aos/agrovoc/c_4145-
dc.subject.agrovocurihttp://aims.fao.org/aos/agrovoc/c_35197-
dc.subject.lcshurihttp://id.loc.gov/authorities/subjects/sh85084301-
dc.description.researchgroupidCOL0015339spa
dc.description.researchgroupidCOL0015099spa
dc.description.researchgroupidCOL0015329spa
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D000977-
dc.relation.ispartofjournalabbrevMoleculesspa
Aparece en las colecciones: Artículos de Revista en Ciencias Exactas y Naturales

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