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Prasugrel
| 品牌 | 厂商性质 | 产地 | 货期 |
|---|---|---|---|
| 阿拉丁 | 生产商 | 上海 | 现货 |
产品参数
| 货号 | CAS号 | 操作 |
|---|---|---|
| P125739-100mg | 150322-43-3 | 询价 |
| P125739-1g | 150322-43-3 | 询价 |
| P125739-500mg | 150322-43-3 | 询价 |
| P125739-5g | 150322-43-3 | 询价 |
产品介绍
- 分子式 C20H20FNO3S
- 分子量373.44
- Beilstein号
- EC号 MFCD09954140
- MDL号 MFCD09954140
- PubChem编号
属性
| 敏感性 | 对热敏感 |
| 溶解性 | Soluble in water (30 mg/ml at 25 °C), DMSO (<1 mg/ml at 25 °C), and ethanol (7 mg/ml at 25 °C). |
| 存贮条件 | 储存温度2-8℃ |
描述
| 应用 | An ADP receptor inhibitor |
| 产品介绍 | Is a member of the thienopyridine class of ADP receptor inhibitors |
| 备注 | A novel platelet inhibitor |
| 生化机理 | Prasugrel is a member of the thienopyridine class of ADP receptor inhibitors. These agents reduce the aggregation ("clumping") of platelets by irreversibly binding to P2Y12 receptors. Prasugrel is a novel platelet inhibitor used for the reduction of thrombotic cardiovascular events (including stent thrombosis) in patients with acute coronary syndrome who are to be managed with PCI. Prasugrel reduces the aggregation ("clumping") of platelets by irreversibly binding to P2Y12 receptors. In rat platelets, prasugrel AM inhibited in vitro platelet aggregation induced by ADP (10 μm) with an IC50 value of 1.8 μm. From Wikipedia |
| 别名 | 普拉格雷;5-[2-环丙基-1-(2-氟苯基)-2-氧乙基]-4,5,6,7-四氢噻吩并[3,2-c]吡啶-2-基羧酸酯;CS 747;LY640315;5-[2-Cyclopropyl-1-(2-fluorophenyl)-2-oxoethyl]-4,5,6,7-tetrahydrothieno[3,2-c]pyridin-2-yl Acetate |
Prasugrel信息由上海阿拉丁生化科技股份有限公司为您提供，如您想了解更多关于Prasugrel报价、型号、参数等信息，欢迎来电或留言咨询。
注：该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案，不可用于临床诊断或治疗等相关用途