Aryl ethynyl anthraquinones: a useful platform for targeting telomeric G-quadruplex structures

Org Biomol Chem. 2014 Jun 14;12(22):3744-54. doi: 10.1039/c4ob00220b. Epub 2014 May 1.

Abstract

Aryl ethynyl anthraquinones have been synthesized by Sonogashira cross-coupling and evaluated as telomeric G-quadruplex ligands, by the FRET melting assay, circular dichroism, the DNA synthesis arrest assay and molecular docking. Both the binding properties and G-quadruplex vs. duplex selectivity are controlled by the structures of the aryl ethynyl moieties.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anthraquinones / chemistry*
  • Circular Dichroism
  • DNA / chemistry
  • Fluorescence
  • G-Quadruplexes*
  • Ligands
  • Models, Molecular
  • Taq Polymerase / metabolism
  • Telomere / chemistry*
  • Transition Temperature

Substances

  • Anthraquinones
  • Ligands
  • DNA
  • Taq Polymerase