Novel dinucleoside 5',5'-triphosphate cap analogues. Synthesis and affinity for murine translation factor eIF4E

Nucleosides Nucleotides Nucleic Acids. 2005;24(5-7):629-33. doi: 10.1081/ncn-200060103.

Abstract

Chemical synthesis of a series of novel dinucleoside cap analogues, m7GpppN, where N is formycin A, 3'-O-methylguanosine, 9-beta-D-arabinofuranosyladenine, and isoguanosine, has been performed using our new methodology. The key reactions of pyrophosphate bonds formation were achieved in anhydrous dimethylformamide solutions employing the catalytic properties of zinc salts. Structures of the new cap analogues were confirmed by 1H NMR and 31p NMR spectra. The binding affinity of the new cap analogues for murine eIF4E(28-217) were determined spectroscopically showing the highest association constant for the analogue that contains formycin A.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine
  • Animals
  • Dose-Response Relationship, Drug
  • Eukaryotic Initiation Factor-4E / chemistry*
  • Eukaryotic Initiation Factor-4E / genetics*
  • Formycins / chemistry
  • Guanosine / chemistry
  • Kinetics
  • Magnetic Resonance Spectroscopy
  • Mice
  • Models, Chemical
  • Nucleosides / chemistry*
  • Nucleotides / chemistry
  • Protein Binding
  • RNA Cap Analogs*
  • Spectrophotometry
  • Thermodynamics
  • Vidarabine / chemistry

Substances

  • Eukaryotic Initiation Factor-4E
  • Formycins
  • Nucleosides
  • Nucleotides
  • RNA Cap Analogs
  • Guanosine
  • isoguanosine
  • formycin
  • Vidarabine
  • Adenosine