凝血酶
水蛭素
直接凝血酶抑制剂的发现与发展
化学
凝结
凝血酶生成
抗凝血酶
IC50型
生物化学
血栓调节蛋白
生物物理学
药理学
作者
Dagmar Prasa,L Svendsen,Jörg Stürzebecher
出处
期刊:Thrombosis and Haemostasis
[Georg Thieme Verlag KG]
日期:1997-01-01
卷期号:77 (03): 498-503
被引量:39
标识
DOI:10.1055/s-0038-1655996
摘要
Summary In a thrombin generation test with continuous registration of thrombin activity in plasma we studied the ability of a variety of thrombin inhibitors of different type and mechanism of action to influence the activity of thrombin after activation of the coagulation system. Depending on the inhibitor, the peak of thrombin activity is delayed and/or reduced. By blocking the active site of generated thrombin inhibitors cause a concentration dependent reduction of the thrombin peak and inhibit feed-back reactions of thrombin resulting in a delay of thrombin generation. Highly potent synthetic active-site directed inhibitors (Ki ≤ 20 nM) reduce the thrombin activity formed in plasma after extrinsic or intrinsic activation with the same efficiency (IC50 0.1 - 0.6 μM) as hirudin. The delay and reduction of thrombin generation by inhibitors of the anion-binding exosite 1 of thrombin is only attributed to an inhibition of feed-back reactions of thrombin. For a 50% reduction of thrombin activity in plasma by this type of inhibitors relatively high concentrations were determined.
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