Adverse effects of alkali and acid on the anticoagulant potency of heparin, evaluated with methyl 2-deoxy-2-sulf- amino-α-d-glucopyranoside 3-sulfate as a model compound
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference14 articles.
1. Novel regio- and stereoselective modifications of heparin in alkaline solution. Nuclear magnetic resonance spectroscopic evidence
2. Importance for Blood Anticoagulant Activity of a 2-Sulfate Grou on L-Iduronic Acid Residues in Heparin
3. Base-catalyzed conversion of the a-l-iduronic acid 2-sulfate unit of heparin into a unit of a-l-galacturonic acid, and related reactions
4. Structure of the antithrombin-binding site in heparin.
5. Evidence for a 3-O-sulfated D-glucosamine residue in the antithrombin-binding sequence of heparin.
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1. Quantitative analysis of the major linkage region tetrasaccharides in heparin;Carbohydrate Polymers;2017-02
2. Electrochemical sensor for heparin based on a poly(thionine) modified glassy carbon electrode;Microchimica Acta;2009-10-27
3. Voltammetric study on the interaction of heparin with toluidine blue, and its analytical application;Microchimica Acta;2006-07-28
4. Investigation on the binding site in heparin by spectrophotometry;Talanta;1999-05
5. A Mathematical Model for Interaction of Spectroscopic Probe with Polysaccharides;Spectroscopy Letters;1998-10
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