Journal
CHEMMEDCHEM
Volume 5, Issue 7, Pages 1123-1133Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cmdc.201000129
Keywords
apoptosis; cell selectivity; cytotoxicity polypyridyl ligands; rhodium
Categories
Funding
- Deutsche Forschungsgemeinschaft (DFG)
- Kind-Philipp Foundation of the Stifterverband fur die Deutsche Wissenschaft
Ask authors/readers for more resources
Half-sandwich rhodium(III) polypyridyl (pp) complexes with the metal atom capped by the facial crown thiaether 14,7-trithiacyclononane [9]aneS(3) represent a promising class of apoptosis-inducing potent,cytostatic agents. The necrotic damage caused by the complexes is negligible., In vitro cytotoxicity assays with the human cancer cell lines MCF-7 and HT 29 and immortalized HEK-293 cells indicate that the dicationic kappa(2)N-(imino) complexes [([9]aneS(3))RhCl(pp)](2+) are much more active than monocationic complexes [([9]aneS(3))RhCl(2)(L)(+) (L=imidazole, CH(3)CN). Whereas the kappa(2)N(amino) complex [([9]aneS(3))RhCl(piperazine)](2+) is inactive, replacing piperazine with the structurally analogous x'S (thiaether) ligand 1,4-dithiane restores cytotoxicity as evidenced by IC(50) values in the range 8.1-11.6 mu m. Spectroscopic (CD, UV/Vis, NOESY) and viscosity measurements indicate that the active dppz complex 8 (IC(50) values: 4.7-8.9 mu m) exhibits strong intercalative binding towards DNA whereas the even more potent bipyrimidine complex 9 (IC(50) values: 0.6-1.9 mu m) causes no alteration of the duplex B conformation. Weaker intercalative binding is observed for the dpq complex 7. A comparative annexin V-propidium iodide binding assay with lymphoma (BJAB) cells and healthy leukocytes demonstrates that the cytotoxic activity of complex 8 and particularly complex 9 is highly selective towards the malignant cells.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available