Ticlopidine hydrochloride is a selective P2Y12 receptor antagonist. Ticlopidine hydrochloride inhibits ADP-induced platelet aggregation and displays antithrombotic activity following oral administration in vivo.
| Molecular Weight | 300.25 |
| Formula | C14H14ClNS.HCl |
| CAS Number | 53885-35-1 |
| Solubility (25°C) | Soluble in Methanol |
| Storage |
Powder -20°C 3 years ; 4°C 2 years In solvent -80°C 6 months ; -20°C 1 month |
| Species | Mouse | Rat | Rabbit | Guinea pig | Hamster | Dog |
| Weight (kg) | 0.02 | 0.15 | 1.8 | 0.4 | 0.08 | 10 |
| Body Surface Area (m2) | 0.007 | 0.025 | 0.15 | 0.05 | 0.02 | 0.5 |
| Km factor | 3 | 6 | 12 | 8 | 5 | 20 |
| Animal A (mg/kg) = Animal B (mg/kg) multiplied by | Animal B Km |
| Animal A Km |
For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.
[1] Stephen D Wiviott, et al. Prasugrel
[2] R Macko. Ticlopidine hydrochloride and prevention of stroke
[3] J F Rothrock, et al. Ticlopidine hydrochloride use and threatened stroke
[4] M K Ito, et al. Ticlopidine: a new platelet aggregation inhibitor
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