Chemical Approaches to Define the Structure-Activity Relationship of Heparin-like Glycosaminoglycans

This publication has 173 references indexed in Scilit:

• Synthesis of Glycosaminoglycan Oligosaccharides − An Unexpected Inhibitory Effect of a Remote N‐Acetyl Group upon Trichloroacetimidate‐Mediated Couplings
  European Journal of Organic Chemistry, 2004
• Efficient Preparation of Three Building Blocks for the Synthesis of Heparan Sulfate Fragments: Towards the Combinatorial Synthesis of Oligosaccharides from Hypervariable Regions
  European Journal of Organic Chemistry, 2003
• Chemical Contributions to Understanding Heparin Activity: Synthesis of Related Sulfated Oligosaccharides
  European Journal of Organic Chemistry, 2003
• Order out of complexity – protein structures that interact with heparin
  Current Opinion in Structural Biology, 2001
• Experimental Proof for the Structure of a Thrombin-Inhibiting Heparin Molecule
  Chemistry – A European Journal, 2001
• Glycosaminoglycans Can Influence Fibroblast Growth Factor-2 Mitogenicity without Significant Growth Factor Binding
  Biochemical and Biophysical Research Communications, 1997
• 1H and 13C NMR spectral assignments of the major sequences of twelve systematically modified heparin derivatives
  Carbohydrate Research, 1996
• Distinct Role of 2-O-, N-, and 6-O-Sulfate Groups of Heparin in the Formation of the Ternary Complex with Basic Fibroblast Growth Factor and Soluble FGF Receptor-1
  Biochemical and Biophysical Research Communications, 1994
• Biologically active heparin-like fragments with a “non-glycosamino”glycan structure. Part 1: a pentasaccharide containing a 3-O-methyl iduronic acid unit.
  Bioorganic & Medicinal Chemistry Letters, 1992
• A new, highly potent, heparin-like pentasaccharide fragment containing a glucose residue instead of a glucosamine
  Bioorganic & Medicinal Chemistry Letters, 1991