202649-52-3Relevant academic research and scientific papers
Pentasaccharides processes for their preparation and pharmaceutical compositions containing them
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Page column 8, (2008/06/13)
Pentasaccharides in acidic form and their pharmaceutically acceptable salts, the anionic form thereof having the formula: wherein: R represents hydrogen or an —SO3?, (C1-C3)alkyl or (C2-C3)
Synthesis of conformationally locked L-iduronic acid derivatives: Direct evidence for a critical role of the skew-boat 2S0 conformer in the activation of antithrombin by heparin
Das, Sanjoy K.,Mallet, Jean-Maurice,Esnault, Jacques,Driguez, Pierre-Alexandre,Duchaussoy, Philippe,Sizun, Philippe,Herault, Jean-Pascal,Herbert, Jean-Marc,Petitou, Maurice,Sinay, Pierre
, p. 4821 - 4834 (2007/10/03)
We have used organic synthesis to understand the role of L-iduronic acid conformational flexibility in the activation of antithrombin by heparin. Among known synthetic analogues of the genuine pentasaccharidic sequence representing the antithrombin bindin
Synthesis of conformationally locked carbohydrates: A skew-boat conformation of L-iduronic acid governs the antithrombotic activity of heparin
Das, Sanjoy K.,Mallet, Jean-Maurice,Esnault, Jacques,Driguez, Pierre-Alexandre,Duchaussoy, Philippe,Sizun, Philippe,Herault, Jean-Pascal,Herbert, Jean-Marc,Petitou, Maurice,Sinay, Pierre
, p. 1670 - 1673 (2007/10/03)
Conformational flexibility of L-iduronic acid is a key feature of this typical component of heparin. Three pentasaccharides have now been synthesized, which are analogues of the active site of heparin and in which the single L-iduronic acid is conformatio
