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dc.creatorElías Rodríguez, María del Pilares
dc.creatorMoreno Clavijo, Elenaes
dc.creatorCarrión Jiménez, Sebastiánes
dc.creatorCarmona Asenjo, Ana Teresaes
dc.creatorMoreno Vargas, Antonio Josées
dc.creatorCaffa, I.es
dc.creatorMontecucco, F.es
dc.creatorCea, M.es
dc.creatorNencioni, A.es
dc.creatorRobina Ramírez, Inmaculadaes
dc.date.accessioned2020-06-02T10:21:15Z
dc.date.available2020-06-02T10:21:15Z
dc.date.issued2014
dc.identifier.citationElías Rodríguez, M.d.P., Moreno Clavijo, E., Carrión Jiménez, S., Carmona Asenjo, A.T., Moreno Vargas, A.J., Caffa, I.,...,Robina Ramírez, I. (2014). Synthesis and cancer growth inhibitory activities of 2-fatty-alkylated pyrrolidine-3,4-diol derivatives. Arkivoc, 3, 197-214.
dc.identifier.issn1551-7012 (impreso)es
dc.identifier.issn1551-7004 (electrónico)es
dc.identifier.urihttps://hdl.handle.net/11441/97346
dc.description.abstractA series of new amphiphilic pyrrolidines containing dodecyl and oleyl apolar side chains were prepared and evaluated for their ability to inhibit the growth of pancreatic ductal adenocarcinoma cells in vitro. The new compounds are shown to exhibit anticancer activity at concentrations in the μM range.es
dc.formatapplication/pdfes
dc.format.extent18 p.es
dc.language.isoenges
dc.publisherArkat USAes
dc.relation.ispartofArkivoc, 3, 197-214.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAmphiphilic compoundses
dc.subjectPyrrolidineses
dc.subjectIminoalditolses
dc.subjectPancreatic canceres
dc.titleSynthesis and cancer growth inhibitory activities of 2-fatty-alkylated pyrrolidine-3,4-diol derivativeses
dc.typeinfo:eu-repo/semantics/articlees
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessrightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Química orgánicaes
dc.relation.publisherversionhttp://dx.doi.org/10.3998/ark.5550190.p008.492es
dc.identifier.doi10.3998/ark.5550190.p008.492es
dc.journaltitleArkivoces
dc.publication.issue3es
dc.publication.initialPage197es
dc.publication.endPage214es

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