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Pathway Description
Argatroban Mechanism of Action Action Pathway
Homo sapiens
Drug Action Pathway
Argatroban is a selective thrombin inhibitor that binds reversibly to the catalytic site and anion-binding exosite inhibiting the cleavage of fibrinogen into fibrin. Unlike bivalirudin, argatroban is not a synthetic peptide but a derivative of L-arginine. Argatroban is used to treat heparin-induced thrombocytopenia as well as to prevent thrombosis. It is used in patients that are undergoing percutaneous coronary intervention or who have a risk in acute coronary syndromes caused by unstable angina or non-ST segment elevation. Thrombin is an important proteinase as it cleaves fibrinogen into fibrin monomers which help form the thrombus that forms the clot at the site of vascular injury. Because Argatroban inhibits thrombin, clotting cannot form which is ideal for heart surgeries and some heart conditions. Argatroban should be monitored as it inhibits clotting so other injuries won't clot and it also can cause blood stagnation. Monitoring changes in hematocrit and blood pressure is extremely important when taking this drug. It is normally administered intravenously so that it is delivered to the site of action right away and can be controlled more easily.
References
Argatroban Mechanism of Action Pathway References
Jennings LK, Saucedo JF: Antiplatelet and anticoagulant agents: key differences in mechanisms of action, clinical application, and therapeutic benefit in patients with non-ST-segment-elevation acute coronary syndromes. Curr Opin Cardiol. 2008 Jul;23(4):302-8. doi: 10.1097/HCO.0b013e3283021ad9.
Pubmed: 18520712
Walker CP, Royston D: Thrombin generation and its inhibition: a review of the scientific basis and mechanism of action of anticoagulant therapies. Br J Anaesth. 2002 Jun;88(6):848-63. doi: 10.1093/bja/88.6.848.
Pubmed: 12173205
Laine M, Lemesle G, Dabry T, Panagides V, Peyrol M, Paganelli F, Bonello L: Bivalirudin during percutaneous coronary intervention in acute coronary syndromes. Expert Opin Pharmacother. 2019 Feb;20(3):295-304. doi: 10.1080/14656566.2018.1551361. Epub 2018 Dec 4.
Pubmed: 30513232
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