Synthesis of novel cyclic NGR/RGD peptide analogs via on resin click chemistry

Bioorg Med Chem Lett. 2010 Dec 15;20(24):7337-40. doi: 10.1016/j.bmcl.2010.10.064. Epub 2010 Oct 21.

Abstract

Targeted drug deliveries as well as high resolution imaging of cancerous tissues and organs via specific cancer cell markers have become important in chemotherapeutic interventions of cancer treatment. Short peptides such as RGD and NGR are showing promising results for targeted drug delivery and in vivo imaging. We have applied on resin Huisgen's 1,3-dipolar cycloaddition to synthesize new cyclic RGD and NGR peptide analogs. Preliminary binding assays of these new analogs by fluorescence polarization indicates specific binding to purified CD13 (Aminopeptidase N) and cell lysates from MCF-7 and SKOV-3 cancer cell lines.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • CD13 Antigens / chemistry
  • CD13 Antigens / metabolism
  • Cell Line, Tumor
  • Click Chemistry
  • Cyclization
  • Drug Carriers / chemistry
  • Fluorescence Polarization
  • Humans
  • Peptides, Cyclic / administration & dosage
  • Peptides, Cyclic / chemical synthesis*
  • Peptides, Cyclic / chemistry
  • Protein Binding
  • Resins, Synthetic / chemistry*

Substances

  • Drug Carriers
  • Peptides, Cyclic
  • Resins, Synthetic
  • cyclic arginine-glycine-aspartic acid peptide
  • CD13 Antigens