New synthetic route for RGD tripeptide

Prep Biochem Biotechnol. 2006;36(3):243-52. doi: 10.1080/10826060600716661.

Abstract

A new route was employed to synthesize RGD. First, Gly-Asp dipeptide was synthesized by a novel chemical method in two steps, including chloroacetylation of L-aspartic acid and ammonolysis of chloroacetyl L-aspartic acid. Second, Nalpha-Z- L-Arginine was reacted with Gly-Asp to synthesize RGD by the N-carboxyanhydride method. Less protected amino acids were used in this synthesis. This method possessed advantages of low cost, simplicity, and rapidity with a reasonable yield of 62% calculated from arginine. In addition, compared with the above method, a conventional solid phase method was also used to synthesize RGD, the yield was 75% calculated from the first amino acid anchored to resin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatography, High Pressure Liquid
  • Molecular Structure
  • Oligopeptides / chemical synthesis*
  • Oligopeptides / chemistry

Substances

  • Oligopeptides
  • arginyl-glycyl-aspartic acid