Chiral platinum(II) metallointercalators with potent in vitro cytotoxic activity

Four platinum(II) metallointercalating complexes of 1,10-phenanthroline (phen) with the chiral ancillary ligands trans-R,R- and trans-S,S-1,2-diaminocyclohexane (R,R- and S,S-dach, respectively), and N,N'-dimethyl-R,R- and N,N'-dimethyl-S,S-1,2-diaminocyclohexane (Me-2-R,R-dach and Me,-S,S-dach, respectively) have been synthesised and characterised. The crystal structure of [Pt(Me-2-S,S-dach)(phen)](ClO4)(2)center dot 1.5 H2O (C20H26Cl2N4O9.5Pt) has been determined; orthorhombic, space group P2(1)2(1)2(1)(No. 19), a=23.194(8), b=25.131(9), c=8.522(3)A. In vitro cytotoxic assays (IC50) in the human bladder cancer cell fine 5637 and in the murine leukemia L1210 cell line revealed that [Pt(S,S-dach)-(phen)](ClO4)(2)(0.091 and 0.13 mu m, respectively) and[Pt(R,R-dach)(phen)](ClO4)(2) (0.54 and 1.50 mu m, respectively) were more cytotoxic than cisplatin (0.31 and 0.50 mu m, respectively) and considerably more cytotoxic than their methylated counterparts, [Pt(Me-2-R,R-dach)(phen)](ClO4)(2) and [Pt(Me-2-S,S-dach)(phen)]ClO4)(2) (both > 1 23 mu m). Chiral discrimination for [Pt(S,S-dach)(phen)](ClO4)(2) over its R,R-enantiomer was observed in all 13 cancer cell lines investigated. Moreover, [Pt(S,S-dach)(phen)](ClO4)(2) was more active than cisplatin in oil cell lines tested and shows only partial cross-resistance to cisplatin in two cisplatin resistant cell lines.