Anticancer activity of new organo-ruthenium, rhodium and iridium complexes containing the 2-(pyridine-2-yl)thiazole N,N-chelating ligand

نویسندگان

  • Michaël Gras
  • Bruno Therrien
  • Georg Süss-Fink
  • Angela Casini
  • Fabio Edafe
  • Paul J. Dyson
چکیده

The dinuclear dichloro complexes [(g-arene)2Ru2(l-Cl)2Cl2] and [(g-C5Me5)2M2(l-Cl)2Cl2] react with 2-(pyridine-2-yl)thiazole (pyTz) to afford the cationic complexes [(g-arene)Ru(pyTz)Cl] (arene = C6H6 1, p-PrC6H4Me 2 or C6Me6 3) and [(g-C5Me5)M(pyTz)Cl] (M = Rh 4 or Ir 5), isolated as the chloride salts. The reaction of 2 and 3with SnCl2 leads to the dinuclear heterometallic trichlorostannyl derivatives [(gp-PrC6H4Me)Ru(pyTz)(SnCl3)] (6) and [(g-C6Me6)Ru(pyTz)(SnCl3)] (7), respectively, also isolated as the chloride salts. The molecular structures of 4, 5 and 7 have been established by single-crystal X-ray structure analyses of the corresponding hexafluorophosphate salts. The in vitro anticancer activities of the metal complexes on human ovarian cancer cell lines A2780 and A2780cisR (cisplatin-resistant), as well as their interactions with plasmid DNA and the model protein ubiquitin, have been investigated.

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تاریخ انتشار 2010