Ru(II)–thyminate complexes : new metallodrug candidates against tumor cells.

dc.contributor.authorCorrea, Rodrigo de Souza
dc.contributor.authorFreire, Vitória
dc.contributor.authorBarbosa, Marília Imaculada Frazão
dc.contributor.authorBezerra, Daniel Pereira
dc.contributor.authorBomfim, Larissa Mendes
dc.contributor.authorMoreira, Diogo Rodrigo de Magalhães
dc.contributor.authorSoares, Milena Botelho Pereira
dc.contributor.authorEllena, Javier Alcides
dc.contributor.authorBatista, Alzir Azevedo
dc.date.accessioned2019-05-08T15:41:41Z
dc.date.available2019-05-08T15:41:41Z
dc.date.issued2018
dc.description.abstractHerein, we used thymine (HThy) as a ligand to form two new ruthenium(II) complexes with formula [Ru(PPh3)2(Thy)(bipy)]PF6 (1) and [Ru(Thy)(bipy)(dppb)]PF6 (2). The complexes were characterized by spectroscopic, spectrometric and X-ray crystallography analyses. Complexes 1 and 2 can interact with ctDNA presenting binding constants, Kb, of 0.4 and 1.2 × 103 M−1, respectively. Their cytotoxic activities towards tumor cell lines (B16-F10, HepG2, K562 and HL-60) and non-tumor cells (PBMCs) were evaluated using the Alamar blue assay. Complex 1 exhibits high cytotoxicity against tumor cells, showing IC50 values of 0.01 and 1.81 μM against the HL-60 and HepG2 cell lines, respectively. Therefore, compound 1 can be considered as a promising antitumor metallodrug.pt_BR
dc.identifier.citationCORREA, R. de S. et al. Ru(II)–thyminate complexes : new metallodrug candidates against tumor cells. New Journal of Chemistry, v. 42, p. 6794--6802, 2018. Disponível em: <https://pubs.rsc.org/en/content/articlelanding/2018/nj/c7nj04368f#!divAbstract>. Acesso em: 7 mar. 2019.pt_BR
dc.identifier.doihttp://doi.org/10.1039/c7nj04368fpt_BR
dc.identifier.issn1369-9261
dc.identifier.urihttp://www.repositorio.ufop.br/handle/123456789/11226
dc.identifier.uri2https://pubs.rsc.org/en/content/articlelanding/2018/NJ/C7NJ04368F#!divAbstractpt_BR
dc.language.isoen_USpt_BR
dc.rightsrestritopt_BR
dc.titleRu(II)–thyminate complexes : new metallodrug candidates against tumor cells.pt_BR
dc.typeArtigo publicado em periodicopt_BR
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