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p-Cymene Complexes of Ruthenium(II) as Antitumor Agents

In this work, the cytotoxic behavior of six ruthenium(II) complexes of stoichiometry [(η(6)-p-cymene)RuCl(2)L] (I-VI), L = 4-cyanopyridine (I), 2-aminophenol (II), 4-aminophenol (III), pyridazine (IV), and [(η(6)-p-cymene)RuClL(2)]PF(6); L = cyanopyridine (V), L = 2-aminophenol(VI) towards three cel...

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Detalles Bibliográficos
Autores principales: Pujante-Galián, María Angeles, Pérez, Sergio A., Montalbán, Mercedes G., Carissimi, Guzmán, Fuster, Marta G., Víllora, Gloria, García, Gabriel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7662397/
https://www.ncbi.nlm.nih.gov/pubmed/33142775
http://dx.doi.org/10.3390/molecules25215063
Descripción
Sumario:In this work, the cytotoxic behavior of six ruthenium(II) complexes of stoichiometry [(η(6)-p-cymene)RuCl(2)L] (I-VI), L = 4-cyanopyridine (I), 2-aminophenol (II), 4-aminophenol (III), pyridazine (IV), and [(η(6)-p-cymene)RuClL(2)]PF(6); L = cyanopyridine (V), L = 2-aminophenol(VI) towards three cell lines was studied. Two of them, HeLa and MCF-7, are human carcinogenic cells from cervical carcinoma and human breast cancer, respectively. A comparison with healthy cells was carried out with BGM cells which are monkey epithelial cells of renal origin. The behavior of complex II exhibits selectivity towards healthy cells, which is a promising feature for use in cancer treatment since it might reduce the side effects of most current therapies.