Feasible synthesis and biological properties of six ‘non-glycosamino’ glycan analogues of the antithrombin III binding heparin pentasaccharide-Reference-Cited by-同舟云学术

Feasible synthesis and biological properties of six ‘non-glycosamino’ glycan analogues of the antithrombin III binding heparin pentasaccharide

Published:1994-11 Issue:11 Volume:2 Page:1267-1280
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Westerduin P.,van Boeckel C.A.A.,Basten J.E.M.,Broekhoven M.A.,Lucas H.,Rood A.,van der Heijden H.,van Amsterdam R.G.M.,van Dinther T.G.,Meuleman D.G.,Visser A.,Vogel G.M.T.,Damm J.B.L.,Overklift G.T.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference47 articles.

1. Structure and Biological Activity of Heparin

2. Hemorrhagic doses of heparin and other glycosaminoglycans induce a platelet defect

3. Antithrombotic and bleeding effects of glycosaminoglycans with different degrees of sulphation

4. Lack of Relationship Between Enhanced Bleeding Induced by Heparin and Other Sulfated Polysaccharides and Enhanced Catalysis of Thrombin Inhibition

Cited by 80 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis of a Heparinoid Pentasaccharide Containing l-Guluronic Acid Instead of l-Iduronic Acid with Preserved Anticoagulant Activity;The Journal of Organic Chemistry;2022-11-21

2. Using NMR to Dissect the Chemical Space and O-Sulfation Effects within the O- and S-Glycoside Analogues of Heparan Sulfate;ACS Omega;2022-07-08

3. Chemical synthesis and pharmacological properties of heparin pentasaccharide analogues;European Journal of Medicinal Chemistry;2022-04

4. An Efficient Modular One-Pot Synthesis of Heparin-Based Anticoagulant Idraparinux;Journal of the American Chemical Society;2019-06-03

5. Design, synthesis, and biomedical applications of synthetic sulphated polysaccharides;Chemical Society Reviews;2019