Prasugrel hydrochloride is a platelet inhibitor with IC50 value of 1.8 μM.
Prasugrel Hydrochloride is an inhibitor of P2Y12. Prasugrel Hydrochloride irreversibly binds to P2Y12 receptors and inhibits platelets. This chemical is a novel third-generation thienopyridine. Prasugrel hydrochloride showed greater platelet inhibition and decreased incidence of ischemic events when compared to clopidogrel.
动物 A (mg/kg) = 动物 B (mg/kg)×动物 B的Km系数/动物 A的Km系数 | |
例如,已知某工具药用于小鼠的剂量为88 mg/kg , 则用于大鼠的剂量换算方法:将88 mg/kg 乘以小鼠的Km系数(3),再除以大鼠的Km系数(6),得到该药物用于大鼠的等效剂量44 mg/kg。
[1] Sugidachi A, et al. The greater in vivo antiplatelet effects of prasugrel as compared to clopidogrel reflect more efficient generation of its active metabolite with similar antiplatelet activity to that of clopidogrel's active metabolite. J Thromb Haemost. 2007 Jul;5(7):1545-51. Epub 2007 Apr 19.
[2] Baker WL, et al. Role of prasugrel, a novel P2Y(12) receptor antagonist, in the management of acute coronary syndromes. Am J Cardiovasc Drugs. 2009;9(4):213-29.
分子式 C20H21ClFNO3S |
分子量 409.9 |
CAS号 389574-19-0 |
储存方式 -20 ℃长期冷藏储存。冰袋运输 |
溶剂(常温) |
DMSO 49 mg/mL |
Water <1 mg/mL |
Ethanol 11 mg/mL |
体内溶解度
注:以上所有数据均来自公开文献,并不保证对所有实验均有效,数据仅供参考。
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