"Self-activating" chemical nuclease: ferrocenyl cyclen Cu(II) complexes act as efficient DNA cleavage reagents in the absence of reductant

Eur J Med Chem. 2009 Apr;44(4):1768-72. doi: 10.1016/j.ejmech.2008.03.029. Epub 2008 Apr 4.

Abstract

The interactions of cyclen Cu(II) complexes functionalized by ferrocenyl group with plasmid DNA indicated that these complexes have high cleavage efficiency via an oxidative mechanism in the absence of any reductant or oxidant.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Copper / chemistry*
  • DNA / metabolism*
  • DNA Cleavage / drug effects*
  • Ferrous Compounds / chemistry*
  • Indicators and Reagents / chemical synthesis
  • Indicators and Reagents / chemistry
  • Indicators and Reagents / metabolism
  • Indicators and Reagents / pharmacology
  • Ligands
  • Metallocenes
  • Organometallic Compounds / chemical synthesis
  • Organometallic Compounds / chemistry
  • Organometallic Compounds / metabolism*
  • Organometallic Compounds / pharmacology*
  • Reducing Agents / metabolism

Substances

  • Ferrous Compounds
  • Indicators and Reagents
  • Ligands
  • Metallocenes
  • Organometallic Compounds
  • Reducing Agents
  • Copper
  • DNA
  • ferrocene