Structure‐Activity Relationships of Synthetic Heparin Fragments
- 1 June 1989
- journal article
- Published by Wiley in Annals of the New York Academy of Sciences
- Vol. 556 (1) , 489-491
- https://doi.org/10.1111/j.1749-6632.1989.tb22546.x
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Synthesis of a potent antithrombin activating pentasaccharide: A new heparin-like fragment containing two 3-O-sulphated glucosaminesTetrahedron Letters, 1988
- Conformational analysis of synthetic heparin‐like oligosaccharides containing α‐L‐idopyranosyluronic acidRecueil des Travaux Chimiques des Pays-Bas, 1987
- Synthesis of an analogue of the antithrombin binding region of heparin containing α‐L‐idopyranoseRecueil des Travaux Chimiques des Pays-Bas, 1987
- Synthesis and conformational analysis of an analogue of the antithrombin-binding region of heparin: The role of the carboxylate function of α-L-idopyranuronateRecueil des Travaux Chimiques des Pays-Bas, 1987
- Synthesis of an antithrombin binding heparin-like pentasaccharide lacking 6-0 sulphate at its reducing end.Tetrahedron Letters, 1986
- Evidence for conformational equilibrium of the sulfated L-iduronate residue in heparin and in synthetic heparin mono- and oligo-saccharides: NMR and force-field studiesJournal of the American Chemical Society, 1986
- Synthesis of a Pentasaccharide Corresponding to the Antithrombin III Binding Fragment of HeparinJournal of Carbohydrate Chemistry, 1985
- Total synthesis of a heparin pentasaccharide fragment having high affinity for antithrombin IIICarbohydrate Research, 1984
- STRUCTURAL STUDIES ON A BIOLOGICALLY ACTIVE HEXASACCHARIDE OBTAINED FROM HEPARINAnnals of the New York Academy of Sciences, 1981
- Assay of heparin in plasma using a chromogenic substrate for activated factor XThrombosis Research, 1976