| 货号 | 规格 | 价格 | 上海 | 北京 | 珠海 | 重庆 | 武汉 | 购买数量 |
|---|---|---|---|---|---|---|---|---|
S65101-5mg买3赠1 |
99.80% | ￥40.00 |
>10 | - | - | - | - |
|
S65101-25mg买3赠1 |
99.80% | ￥89.00 |
>10 | - | - | - | - |
|
S65101-100mg买3赠1 |
99.80% | ￥235.00 |
>10 | - | 2 | - | - |
|
S65101-250mg买3赠1 |
99.80% | ￥398.00 |
>10 | - | - | - | - |
|
S65101-500mg买3赠1 |
99.80% | ￥680.00 |
>10 | - | - | - | - |
|
| 体内研究： | In rat platelets, Prasugrel hydrochloride active metabolite inhibits in vitro platelet aggregation induced by adenosine ADP (10μM) with an IC50 value of 1.8 μM. Prasugrel hydrochloride acts faster and is significantly more potent than Clopidogrel in vivo. Prasugrel hydrochloride is an inactive prodrug that requires metabolic processing in vivo to generate the active antiplatelet metabolite. Prasugrel hydrochloride is rapidly absorbed from the gut. 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. |
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| 保存条件： | RT | ||||||||||||||||||||
| 配置溶液浓度参考： |
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| 注意： | 部分产品我司仅能提供部分信息，我司不保证所提供信息的权威性，仅供客户参考交流研究之用。 |
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