| Bioactivity | Prasugrel chloride impurity is a catp impurity of Prasugrel, exacted from patent US20130345428A1, line 0053. Prasugrel is an orally active and potent P2Y12 receptor antagonist, and inhibits ADP-induced platelet aggregation[1][2]. |
| Name | Prasugrel chloride impurity |
| CAS | 1056459-37-0 |
| Formula | C20H21ClFNO3S |
| Molar Mass | 409.90 |
| Transport | Room temperature in continental US; may vary elsewhere. |
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
| Reference | [1]. Hiroyuki Miyata, et al. Method for production of prasugrel hydrochloride having high purity. US20130345428A1. [2]. 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. |
Prasugrel chloride impurity
CAS: 1056459-37-0 F: C20H21ClFNO3S W: 409.90
Prasugrel chloride impurity is a catp impurity of Prasugrel, exacted from patent US20130345428A1, line 0053. Prasugrel i
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