Ticlopidine hydrochloride

• 产品号: S1984
• CAS号: 53885-35-1
• 分子式: C14H15Cl2NS
• 分子量: 300.2466
• 保 存: -20°C

产品别名

• 标题: Ticlopidine hydrochloride
• IUPAC标准名: 5-[(2-chlorophenyl)methyl]-4H,5H,6H,7H-thieno[3,2-c]pyridine hydrochloride
• IUPAC传统名: ticlopidine hydrochloride

产品登记号

• CAS号: 53885-35-1

产品性质

• 作用靶点: P2X(7) receptor
• 成盐信息: hydrochloride
• 保存条件: -20°C

产品详细信息

详细说明 (English)

Biological Activity:
Ticlopidine hydrochloride is a hydrochloride salt form of ticlopidine which is a selective P2Y12 receptor antagonist. Ticlopidine hydrochloride inhibits ADP-induced platelet aggregation and exhibits antithrombotic activity following oral administration in vivo. Ticlopidine hydrochloride produces time- and dose-dependent inhibition of both platelet aggregation and release of platelet granule constituents as well as prolongation of bleeding time. Ticlopidine hydrochloride interferes with platelet membrane function by preventing platelet-fibrinogen binding and subsequent platelet-platelet interactions. Ticlopidine hydrochloride is rapidly absorbed with peak levels (Tmax) occurring about 2 after dose. Ticlopidine hydrochloride is greater than 80% absorbed. Administration after meals results in a 20% increase in the AUC. Ticlopidine hydrochloride is 98% bound to plasma proteins. Ticlopidine hydrochloride is metabolized extensively by the liver. Only trace amounts of ticlopidine are detected in urine. [1]References on Ticlopidine HCl[1] Arterioscler Thromb Vasc Biol., 2008 Mar, 28(3):s33-8

参考文献

• Michelson AD. Arterioscler Thromb Vasc Biol. 2008 Mar;28(3):s33-8.