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dc.contributor.authorUpegui Zapata, Yulieth Alexandra-
dc.contributor.authorGil Romero, Juan Fernando-
dc.contributor.authorQuiñones Fletcher, Winston-
dc.contributor.authorTorres, Fernando-
dc.contributor.authorEscobar Peláez, Gustavo-
dc.contributor.authorRobledo Restrepo, Sara María-
dc.contributor.authorEcheverri López, Luis Fernando-
dc.date.accessioned2021-11-02T13:24:53Z-
dc.date.available2021-11-02T13:24:53Z-
dc.date.issued2014-
dc.identifier.citationUpegui, Y., Gil, J., Quiñones, W., Torres, F., Escobar, G., Robledo, S., & Echeverri, F. (2014). Preparation of Rotenone Derivatives and in Vitro Analysis of Their Antimalarial, Antileishmanial and Selective Cytotoxic Activities. Molecules, 19(11), 18911–18922. Retrieved from http://dx.doi.org/10.3390/molecules191118911spa
dc.identifier.issn1420-3049-
dc.identifier.urihttp://hdl.handle.net/10495/23682-
dc.description.abstractABSTRACT: Six derivatives of the known biopesticide rotenone were prepared by several chemical transformations. Rotenone and its derivatives showed differential in vitro antiparasitic activity and selective cytotoxicity. In general, compounds were more active against Plasmodium falciparum than Leishmania panamensis. Rotenone had an EC50 of 19.0 µM against P. falciparum, and 127.2 µM against L. panamensis. Although chemical transformation does not improve its biological profile against P. falciparum, three of its derivatives showed a significant level of action within an adequate range of activity with EC50 values < 50.0 µM. This antiplasmodial activity was not due to red blood cell hemolysis, since LC50 was >>400 µM. On the other hand, all derivatives displayed a non-specific cytotoxicity on several cell lines and primary human cell cultures.spa
dc.format.extent12spa
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.titlePreparation of Rotenone Derivatives and in Vitro Analysis of Their Antimalarial, Antileishmanial and Selective Cytotoxic Activitiesspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupPrograma de Estudio y Control de Enfermedades Tropicales (PECET)spa
dc.publisher.groupQuímica Orgánica de Productos Naturalesspa
dc.identifier.doi10.3390/molecules191118911-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
oaire.citationtitleMoleculesspa
oaire.citationstartpage18911spa
oaire.citationendpage18922spa
oaire.citationvolume19spa
oaire.citationissue11spa
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.decsAntiparasitarios-
dc.subject.decsAntiparasitic Agents-
dc.subject.agrovocRotenona-
dc.subject.agrovocRotenone-
dc.subject.agrovocCitotoxicidad-
dc.subject.agrovocCytotoxicity-
dc.subject.proposalTransformaciones químicasspa
dc.subject.agrovocurihttp://aims.fao.org/aos/agrovoc/c_6665-
dc.subject.agrovocurihttp://aims.fao.org/aos/agrovoc/c_34251-
dc.description.researchgroupidCOL0015339spa
dc.description.researchgroupidCOL0015099spa
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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