dc.contributor.author | Matesanz García, Ana Isabel | |
dc.contributor.author | Jimenez-Faraco, Eva | |
dc.contributor.author | Ruiz, María C. | |
dc.contributor.author | Balsa, Lucia M. | |
dc.contributor.author | Navarro-Ranninger, Carmen | |
dc.contributor.author | León, Ignacio E. | |
dc.contributor.author | Gómez Quiroga, Adoración | |
dc.contributor.other | UAM. Departamento de Química Inorgánica | es_ES |
dc.date.accessioned | 2018-04-23T16:08:25Z | |
dc.date.available | 2018-04-23T16:08:25Z | |
dc.date.issued | 2018-01-01 | |
dc.identifier.citation | Inorganic Chemistry Frontiers 5.1 (2018): 73-83 | en_US |
dc.identifier.issn | 2052-1553 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10486/681764 | |
dc.description.abstract | Two Pd(ii) and Pt(ii) complexes with two pyrrol-2-carbaldehyde N-p-chlorophenylthiosemicarbazone ligands are designed and characterized showing mononuclear structures. An important pharmacological property for both compounds is the high selectivity for tumor cells and a lack of activity in healthy cells. The Pd(ii) compound shows a higher antitumor activity and selectivity than the Pt(ii) compound. Both complexes present a variety of biological interactions: with DNA models (pBR322 and CT DNA), proteins (lysozyme and RNase) and other biological targets like proteosome. Our results show that the Pd(ii) complex is a more interesting candidate for potential anticancer therapies than the Pt(ii) complex, and we provide new insight into the design and synthesis of palladium compounds as potential antitumor agents. | en_US |
dc.description.sponsorship | This work was supported by the following grants for the Spanish MINECO: SAF-2012-34424, CTQ2015-68779R and CTQ2015-70371-REDT | en_US |
dc.format.extent | 11 pag. | es_ES |
dc.format.mimetype | application/pdf | en |
dc.language.iso | eng | en |
dc.publisher | Royal of Society of Chemistry | en_US |
dc.relation.ispartof | Inorganic Chemistry Frontiers | en_US |
dc.rights | © 2017 The Royal Society of Chemistry | en_US |
dc.subject.other | Mononuclear structures | en_US |
dc.subject.other | Tumor cells | en_US |
dc.subject.other | Antitumor activity | en_US |
dc.subject.other | Pd(II) complex | en_US |
dc.subject.other | Potential anticancer therapies | en_US |
dc.title | Mononuclear Pd(II) and Pt(II) complexes with an α-N-heterocyclic thiosemicarbazone: Cytotoxicity, solution behaviour and interaction: Versus proven models from biological media | en_US |
dc.type | article | en |
dc.subject.eciencia | Química | es_ES |
dc.date.embargoend | 2019-01-01 | |
dc.relation.publisherversion | http://doi.org/10.1039/C7QI00446J | es_ES |
dc.identifier.doi | 10.1039/C7QI00446J | es_ES |
dc.identifier.publicationfirstpage | 73 | es_ES |
dc.identifier.publicationissue | 1 | es_ES |
dc.identifier.publicationlastpage | 83 | es_ES |
dc.identifier.publicationvolume | 5 | es_ES |
dc.relation.projectID | Gobierno de España. SAF-2012-34424 | es_ES |
dc.relation.projectID | Gobierno de España. CTQ2015-68779R | es_ES |
dc.relation.projectID | Gobierno de España. CTQ2015-70371-REDT | es_ES |
dc.type.version | info:eu-repo/semantics/acceptedVersion | en |
dc.rights.accessRights | openAccess | en |
dc.facultadUAM | Facultad de Ciencias | |