Coordination Chemistry of the Antitumor Metallocene Molybdocene Dichloride with Biological Ligands

Jenny B. Waern, Margaret M. Harding*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

49 Citations (Scopus)

Abstract

The relative affinity of molybdocene dichloride (Cp2MoCl 2) for the thiol, amino, carboxylate, phosphate(O) and heterocyclic(N) donor ligands present in amino acids and nucleotides, has been studied in aqueous solutions at pH 2-7, using 1H, 13C and 31P NMR spectroscopy. Molybdocene dichloride forms the highly water soluble, air-stable complexes Cp2Mo(Cys)2 and Cp 2Mo(GS)2 with cysteine and glutathione respectively, via coordination of the deprotonated thiol groups. While coordination to the imidazole nitrogen in histidine was observed, no evidence for coordination of the amino or carboxylate groups in the amino acids cysteine, histidine, alanine or lysine to Cp2MoCl2 was detected. Competition experiments with dAMP, ribose monophosphate and histidine showed preferential coordination to the cysteine thiol over the phosphate(O) and heterocyclic(N) groups. Cp2Mo(Cys)2 is stable in the presence of excess dAMP or ribose monophosphate and Cys displaces coordinated histidine, dAMP or ribose monophosphate to give Cp2Mo(Cys)2. These results provide further evidence against interaction with DNA as the key interaction that is related to the antitumor activity of molybdocene dichloride. The implications of these results for the biological activity of the antitumor metallocene and the likely species formed in vivo are discussed.

Original languageEnglish
Pages (from-to)206-213
Number of pages8
JournalInorganic Chemistry
Volume43
Issue number1
DOIs
Publication statusPublished - 12 Jan 2004
Externally publishedYes

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