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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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 |
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. |
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