Synthesis of Conformationally Lockedl-Iduronic Acid Derivatives: Direct Evidence for a Critical Role of the Skew-Boat2S0 Conformer in the Activation of Antithrombin by Heparin-Reference-Cited by-同舟云学术

Synthesis of Conformationally Lockedl-Iduronic Acid Derivatives: Direct Evidence for a Critical Role of the Skew-Boat2S0 Conformer in the Activation of Antithrombin by Heparin

Published:2001-11-19 Issue:22 Volume:7 Page:4821-4834
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Das Sanjoy K.,Mallet Jean-Maurice,Esnault Jacques,Driguez Pierre-Alexandre,Duchaussoy Philippe,Sizun Philippe,Herault Jean-Pascal,Herbert Jean-Marc,Petitou Maurice,Sinaÿ Pierre

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Reference70 articles.

1. Conformational flexibility: a new concept for explaining binding and biological properties of iduronic acid-containing glycosaminoglycans

2. Heparin is essential for the storage of specific granule proteases in mast cells

3. Abnormal mast cells in mice deficient in a heparin-synthesizing enzyme

4. A Novel Role for 3-O-Sulfated Heparan Sulfate in Herpes Simplex Virus 1 Entry

5. Fibroblast growth factor receptor signalling is dictated by specific heparan sulphate saccharides

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