Synthesis and characterization of a novel ester-based nucleoamino acid for the assembly of aromatic nucleopeptides for biomedical applications

Int J Pharm. 2011 Aug 30;415(1-2):206-10. doi: 10.1016/j.ijpharm.2011.06.007. Epub 2011 Jun 13.

Abstract

In this work, we report a technological approach to a novel Fmoc-protected nucleoamino acid, based on l-tyrosine, carrying the DNA nucleobase on the hydroxyl group by means of an ester bond, suitable for the solid-phase synthesis of novel aromatic nucleopeptides of potential interest in biomedicine. After ESI-MS and NMR characterization this building block was used for the assembly of a thymine-functionalized tetrapeptide, composed of nucleobase-containing and underivatized l-tyrosine moieties alternated in the backbone.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / chemical synthesis
  • Amino Acids / chemistry
  • Amino Acids, Aromatic / chemical synthesis*
  • Amino Acids, Aromatic / chemistry
  • Chromatography, Liquid
  • Esters
  • Fluorenes / chemical synthesis
  • Fluorenes / chemistry
  • Molecular Conformation
  • Nuclear Magnetic Resonance, Biomolecular
  • Oligopeptides / chemical synthesis*
  • Oligopeptides / chemistry
  • Peptide Nucleic Acids / chemical synthesis*
  • Peptide Nucleic Acids / chemistry
  • Spectrometry, Mass, Electrospray Ionization
  • Tyrosine / chemistry

Substances

  • Amino Acids
  • Amino Acids, Aromatic
  • Esters
  • Fluorenes
  • N(alpha)-fluorenylmethyloxycarbonylamino acids
  • Oligopeptides
  • Peptide Nucleic Acids
  • Tyrosine