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Ticlopidine is a thienopyridine P2Y12 receptor antagonist.1 It inhibits aggregation of human platelets induced by collagen, arachidonic acid (Item No. 90010), and ADP (Item No. 16778; IC50s = 75, 600, and 1,300 μM, respectively).2 It also inhibits ADP-induced aggregation of rat platelets and decreases thrombus weight in vivo in a rat model of arterio-venous shunt thrombosis when administered at a dose of 100 mg/kg.3 Ticlopidine (300 mg/kg) inhibits healing of acetic acid-induced gastric ulcers in rats.4 Formulations containing ticlopidine have been used in the prevention of thrombotic stroke.
WARNING This product is not for human or veterinary use.
1. Platelet P2Y12 receptor inhibition by thienopyridines: Status and future. Expert Opin. Investig. Drugs 18(9), 1317-1332 (2009).
2. The mechanisms of action of ticlopidine. Thromb. Res. Suppl. 4, 59-67 (1983).
3. The in vivo pharmacological profile of CS-
4. Platelets modulate gastric ulcer healing: Role of endostatin and vascular endothelial growth factor release. Proc. Natl. Acad. Sci. USA 98(11), 6470-6475 (2001).