产品描述
Prasugrel Maleic acid is an orally active and potent P2Y12 receptor antagonist and inhibits ADP-induced platelet aggregation. Prasugrel Maleic acid is a thienopyridine and prodrug. Prasugrel Maleic acid also inhibits platelet function.
体外活性
Prasugrel hydrochloride is an inactive prodrug that requires metabolic processing in vivo to generate the active antiplatelet metabolite. Prasugrel Maleic acid is rapidly absorbed from the gut. Prasugrel Maleic acid active metabolite inhibits in vitro platelet aggregation induced by adenosine ADP (10μM) (IC50: 1.8 μM), in rat platelets. Prasugrel Maleic acid acts faster and is significantly more effective than Clopidogrel in vivo. After oral administration of standard-loading doses of 60 mg, maximum plasma levels of the active metabolite are achieved within 1 h, effective, maximum inhibition of platelet aggregation at 1-2 h[1][2].
Cas No.
389574-20-3
分子式
C24H24FNO7S
分子量
489.51
别名
PCR 4099 (Maleic acid);马来酸普拉格雷;Prasugrel (Maleic acid)
储存和溶解度
(< 1 mg/ml refers to the product slightly soluble or insoluble )
Powder: -20°C for 3 years
In solvent: -80°C for 2 years