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dc.contributor.authorFrança, Paulo H. B.-
dc.contributor.authorSilva-Júnior, Edeildo F. da-
dc.contributor.authorAquino, Pedro G. V.-
dc.contributor.authorSantana, Antônio E. G.-
dc.contributor.authorFerro, Jamylle N. S.-
dc.contributor.authorBarreto, Emiliano de Oliveira-
dc.contributor.authorPessoa, Cláudia do Ó-
dc.contributor.authorMeira, Assuero Silva-
dc.contributor.authorAquino, Thiago M. de-
dc.contributor.authorAlexandre-Moreira, Magna S.-
dc.contributor.authorSchmitt, Martine-
dc.contributor.authorAraújo-Júnior, João X. de-
dc.date.accessioned2016-07-18T13:16:51Z-
dc.date.available2016-07-18T13:16:51Z-
dc.date.issued2016-03-
dc.identifier.citationFRANÇA, P. H. B. et al. Preliminary in vitro evaluation of the anti-proliferative activity of guanylhydrazone derivatives. Acta Pharmaceutica, Zagreb, v. 66, n. 1, p. 129–137, mar. 2016.pt_BR
dc.identifier.issnOn-line 1846-9558-
dc.identifier.urihttp://www.repositorio.ufc.br/handle/riufc/18430-
dc.description.abstractGuanylhydrazones have shown promising antitumor activity in preclinical tumor models in several studies. In this study, we aimed at evaluating the cytotoxic effect of a series of synthetic guanylhydrazones. Different human tumor cell lines, by including HCT-8 (colon carcinoma), MDA-MB-435 (melanoma) and SF-295 (glioblastoma) were continuous exposed to guanylhydrazone derivatives for 72 hours and growth inhibition of tumor cell lines and macrophages J774 was measured using tetrazolium salt (MTT) assay. Compounds 7, 11, 16 and 17 showed strong cytotoxic activity with IC50 values lower than 10 μmol L−1 against four tumor cell lines. Among them, 7 was less toxic to non-tumor cells. Finally, obtained data suggest that guanylhydrazones may be regarded as potential lead compounds for the design of novel anticancer agents.pt_BR
dc.language.isoenpt_BR
dc.publisherActa Pharmaceuticapt_BR
dc.subjectNeoplasias do Colopt_BR
dc.subjectGlioblastomapt_BR
dc.titlePreliminary in vitro evaluation of the anti-proliferative activity of guanylhydrazone derivativespt_BR
dc.typeArtigo de Periódicopt_BR
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