A new phenanthroline-oxazine ligand: synthesis, coordination chemistry and atypical DNA binding interaction

Chem Commun (Camb). 2013 Mar 21;49(23):2341-3. doi: 10.1039/c3cc38710k.

Abstract

1,10-Phenanthroline-5,6-dione and l-tyrosine methyl ester react to form phenanthroline-oxazine (PDT) from which [Cu(PDT)(2)](ClO(4))(2) and [Ag(PDT)(2)]ClO(4)·2MeOH are obtained. Binding to calf-thymus DNA by Ag(I) and Cu(II) PDT complexes exceed bis-1,10-phenanthroline analogues and the minor groove binding drugs, pentamidine and netropsin. Furthermore, unlike the artificial metallonuclease, [Cu(phen)(2)](2+), the [Cu(PDT)(2)](2+) complex does not cleave DNA in the presence of added reductant indicating unique interaction with DNA.

MeSH terms

  • Animals
  • Binding Sites
  • Cattle
  • Coordination Complexes / chemistry
  • Copper / chemistry
  • DNA / chemistry*
  • DNA / metabolism
  • Ligands
  • Molecular Conformation
  • Netropsin / chemistry
  • Oxazines / chemistry*
  • Oxidation-Reduction
  • Pentamidine / chemistry
  • Phenanthrolines / chemistry*
  • Silver / chemistry

Substances

  • Coordination Complexes
  • Ligands
  • Oxazines
  • Phenanthrolines
  • Silver
  • Netropsin
  • Pentamidine
  • Copper
  • DNA
  • calf thymus DNA
  • 1,10-phenanthroline