Data from: Ruthenium(II) complexes of curcumin and β-diketone derivatives: Effect of structural modifications on their cytotoxicity

Ruthenium(II) complexes (Ru1 - Ru3) with the general formula
[Ru(O-O)(PPh3)2(bipy)]PF6, bearing two triphenylphosphine (PPh3),
bipyridine (bipy), and a series of natural and synthetic β-diketones (O,O)
ligands where synthesized and characterized using various analytical
techniques. The interaction between the complexes and calf thymus DNA
(CT-DNA) was investigated, and demonstrated a weak interaction. The
cytotoxicity of the complexes was investigated against breast cancer cells
(MDA-MB-231 and MCF-7), lung cancer cells (A549), cisplatin-resistant
ovarian cancer cells (A2780cis), as well as non-tumor lung (MRC-5) and
non-tumor breast (MCF-10A) cell lines. All complexes exhibited cytotoxic
activity against all the cell lines studied, with IC50 values ranging from
0.39 to 13 µM. Notably, the three complexes demonstrated selectivity
against the A2780cis cell line, with IC50 ranging from 0.39 to 0.82 µM.
Among them, Ru2 exhibited the highest cytotoxicity, with an IC50 value of
0.39 µM. Consequently, this new class of complexes shows good selectivity
towards cisplatin-resistant ovarian cancer cells, and it is promising for
further investigation as anticancer agents.