Synthesis of a potent antithrombin activating pentasaccharide: A new heparin-like fragment containing two 3-O-sulphated glucosamines
- 31 December 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (7) , 803-806
- https://doi.org/10.1016/s0040-4039(00)80214-2
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Conformational analysis of synthetic heparin‐like oligosaccharides containing α‐L‐idopyranosyluronic acidRecueil 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
- Synthesis of a heparin pentasaccharide fragment with a high affinity for antithrombin III employing cellobiose as a key starting materialTetrahedron 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
- Structure-activity relationship in heparin: A synthetic pentasaccharide with high affinity for antithrombin III and eliciting high anti-factor Xa activityBiochemical and Biophysical Research Communications, 1983
- Further characterization of the antithrombin-binding sequence in heparinCarbohydrate Research, 1982
- 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