Catalysis of regioselective reduction of NAD+ by ruthenium(II) arene complexes under biologically relevant conditions

J Biol Inorg Chem. 2006 Jun;11(4):483-8. doi: 10.1007/s00775-006-0098-5. Epub 2006 Apr 8.

Abstract

Ruthenium(II) arene anticancer complexes [(eta6-arene)Ru(en)Cl]PF6 (arene is hexamethylbenzene, p-cymene, indan; en is ethylenediamine) can catalyse regioselective reduction of NAD+ by formate in water to form 1,4-NADH, at pD 7.2, 37 degrees C, and in the presence of air. The catalytic activity is markedly dependent on the arene, with the hexamethylbenzene (hmb) complex showing the highest activity. For [(eta 6-hmb)Ru(en)Cl]PF6, the rate of reaction is independent of NAD+ concentration and shows saturation kinetics with respect to formate concentration. A Km value of 58 mM and a turnover frequency at saturation of 1.46 h(-1) were observed. Removal of chloride and performing the reaction under argon led to higher reaction rates. Lung cancer cells (A549) were found to be remarkably tolerant to formate even at millimolar concentrations. The possibility of using ruthenium arene complexes coadministered with formate as catalytic drugs is discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / pharmacology
  • Benzene Derivatives / chemistry*
  • Benzene Derivatives / pharmacology
  • Catalysis
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Dose-Response Relationship, Drug
  • Humans
  • Magnetic Resonance Spectroscopy
  • Models, Molecular
  • NAD / chemistry*
  • NAD / physiology
  • Organometallic Compounds / chemistry
  • Organometallic Compounds / pharmacology
  • Oxidation-Reduction
  • Ruthenium / chemistry*
  • Ruthenium / pharmacology
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • Benzene Derivatives
  • Organometallic Compounds
  • NAD
  • Ruthenium
  • hexamethylbenzene