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Platinum carboxylato-pendant-arm macrocycles: structure, redox properties and anti-cancer potential.

Abstract
In an attempt to generate new platinum compounds that may be effective in the treatment of cancer, as well as having a lower toxicity than traditional platins and being orally viable, we are studing the synthesis and reactivity of platinum complexes of tetraazamacrocycles bearing carboxylato pendant arms. We have synthesized adducts of meso- and rac-5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane-1,7-diacetic acid (L(1)H(2)). The meso-Pt(II)L(1) complex is unstable with respect to disproportionation, forming platinum metal and [meso-Pt(IV)L(1)](2+). The rac-isomer shows less tendency to disproportionate. Cyclic voltammetry suggests that the rac-Pt(II)L(1) complex undergoes two one-electron oxidations. Using bis-triazacyclononanenickel(III), [Ni(III)(tacn)(2)](3+) as an outer-sphere oxidant, the self-exchange rate for the [Pt(II/III)L](0/+) couple has been estimated at 0.034 M(-1) s(-1).
AuthorsR I Haines, D R Hutchings, T M McCormack
JournalJournal of inorganic biochemistry (J Inorg Biochem) Vol. 85 Issue 1 Pg. 1-7 (May 2001) ISSN: 0162-0134 [Print] United States
PMID11377689 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • Platinum Compounds
Topics
  • Antineoplastic Agents (chemistry)
  • Oxidation-Reduction
  • Platinum Compounds (chemistry)
  • Structure-Activity Relationship

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