Synthesis of cycloruthenated compounds as potential anticancer agents
Leyva, Lida, Sirlin, Claude, Rubio, Laura, Franco, Cecilia, Le Lagadec, Ronan, Spencer, John, Bischoff, Pierre, Gaiddon, Christian, Loeffler, Jean-Philippe and Pfeffer, Michel (2007) Synthesis of cycloruthenated compounds as potential anticancer agents. European Journal of Inorganic Chemistry, 2007 (19). pp. 3055-3066. ISSN 1434-1948 (doi:10.1002/ejic.200601149)Full text not available from this repository.
A library of 19 cycloruthenated derivatives is constructed by making use of the well-known cyclometalation reaction. Their geometries are modified in a straightforward manner by addition of either mono- or bidentate ligands, such as bipyridine, phenanthroline, 1,2-bis(diphenylphosphanyl)ethane, dimethylphenylphosphane, triphenylphosphane, and 1,3,5-triaza-7-phosphatricyclo[126.96.36.199]decane (PTA) ligands, to cationic cycloruthenated centers. The antitumor properties of the compounds thus obtained are investigated in order to compare them with recently reported ruthenium complexes and cisplatin. IC50 values against mammalian cells (A-172, HCT-116, and RDM-4) are determined for the library compounds and some of them, such as those derived from orthoruthenated phenylpyridine and a bidentate N,N ligand, display activity of the same order of magnitude as cisplatin.
|Uncontrolled Keywords:||bioinorganic chemistry, ruthenium, metallacycles, antitumor agents|
|Subjects:||Q Science > QD Chemistry|
R Medicine > RM Therapeutics. Pharmacology
|School / Department / Research Groups:||School of Science|
School of Science > Department of Pharmaceutical, Chemical & Environmental Sciences
|Last Modified:||01 Apr 2011 16:18|
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