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Direct thrombin inhibitors in cardiovascular medicine.
Author(s) -
Jeffrey Lefkovits,
Eric J. Topol
Publication year - 1994
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/01.cir.90.3.1522
Subject(s) - thrombin , discovery and development of direct thrombin inhibitors , medicine , antithrombins , heparin , coagulation , coagulation cascade , pharmacology , ximelagatran , direct thrombin inhibitor , warfarin , anticoagulant , cardiology , platelet , dabigatran , atrial fibrillation
Currently used antithrombotics such as heparin have a number of potential limitations that may be overcome by the new class of agents that directly inhibit thrombin. These agents variously block the active catalytic and/or the anion binding exosites of the thrombin molecule and are potent and specific inhibitors of thrombin's many biological actions, as demonstrated by in vitro and animal models of thrombosis. Preliminary data indicate that the direct antithrombins are safe and efficacious in humans, and their use in acute coronary syndromes and coronary angioplasty in place of heparin has yielded promising early results. Phase III trials in these clinical settings are currently under way. Newer antithrombotics that inhibit thrombin generation and thrombin activity at various strategic points within the coagulation cascade are also in the early stages of development.

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