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. 2008 Dec 16;14(3):439–448. doi: 10.1007/s00775-008-0460-x

Table 2.

Concentration that induces 50% growth inhibition of cells compared with untreated cells (IC50) (μM) of the [Ru(apy)(tpy)L2 n](2−n)+ complexes (1a, 1b, 1c) and their dinuclear analogue [Ru(apy)(tpy)]2[μ-H2N(CH2)6NH2](ClO4)4 (1f) after a 5-day treatment with selected cell lines

Compound tested A498 EVSA-T H226 IGROV M19 MEL MCF7 WIDR
[Ru(apy)(tpy)Cl](ClO4) (1a) >96 7 17 >96 25 13 66
[Ru(apy)(tpy)(H2O)](ClO4)2·2H2O (1b) >81 6 17 44 26 18 50
[Ru(apy)(tpy)(CH3CN)] (ClO4)2 (1c) >82 6 26 78 30 21 73
[Ru(azpy)(tpy)Cl]Cl·5H2O (1d) 39 11 34 65 15 30 51
[Ru(apy)(tpy)]2[μ-H2 N(CH2)6NH2] (ClO4)4 (1f) >40 17 28 >40 33 >40 >40
α-[Ru(azpy)2Cl2] 0.3 0.1 0.5 0.3 0.1 0.3 0.3
Cisplatin 2 1 2 0.2 3 2 2

α-[Ru(azpy)2Cl2] and cisplatin have been included as reference compounds