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Heparin-like compounds, their production and use for inhibiting arterial thrombus due to vascular injury and intervention

机译:肝素样化合物,其生产以及用于抑制由于血管损伤和干预引起的动脉血栓的用途

摘要

The present invention is related to heparin-like compounds characterized by their capacity of inhibiting collagen-induced platelet aggregation in flowing whole blood and their use for prophylactic treatment of arterial thrombosis associated with vascular or microvascular injury and interventions. Said properties are related to a high coupling density of negatively charged heparin or heparin-like glycosaminoglycan molecules, present in multiple heparin or heparin-like glycosaminoglycans as well as in proteoglycans containing said multiple heparin or heparin-like glycosaminoglycans or lower-molecular-weight heparin or heparin-like glycosaminoglycans connected directly or through spacer/linker molecules to globular core molecules. Heparin-like compounds, with said properties are obtainable from mammalian mast cells, by tissue extraction or cell cultivation. The heparin-like compounds of the present invention can also be produced by synthetical, semisynthetical and/or biotechnological methods and they are useful for manufacturing preparations, means and devices for local or topical application in prophylactic treatment of arterial thrombosis and its sequelae.
机译:本发明涉及肝素样化合物,其特征在于其在流动的全血中抑制胶原蛋白诱导的血小板凝集的能力,以及其在与血管或微血管损伤有关的动脉血栓形成的预防性治疗和干预中的用途。所述性质与存在于多种肝素或类肝素糖胺聚糖中以及含有所述多种肝素或类肝素糖胺聚糖或低分子量肝素的蛋白聚糖中的带负电荷的肝素或类肝素糖胺聚糖分子的高偶联密度有关。或肝素样糖胺聚糖直接或通过间隔子/连接子分子连接至球状核心分子。具有所述性质的肝素样化合物可通过组织提取或细胞培养从哺乳动物肥大细胞获得。本发明的肝素样化合物也可以通过合成,半合成和/或生物技术方法生产,并且它们可用于制备用于预防或治疗动脉血栓形成及其后遗症的局部,局部应用的制剂,手段和装置。

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