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My Cart> Small Molecule Compounds > Inhibitors & Antagonists & Agonists > GPCR & G Protein > Prasugrel HydrochlorideCAS：389574-19-0
Molecular Formula：C20H21ClFNO3S
Molecular Weight：409.9
Storage：Powder:2-8℃，2 years;Insolvent(Mother Liquid):-20℃，6 months;-80℃，1 year
Purity：≥98%
Appearance：Light yellow to yellow Solid
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| CAS | 389574-19-0 |
| Name | Prasugrel Hydrochloride |
| Molecular Formula | C20H21ClFNO3S |
| Molecular Weight | 409.9 |
| Solubility | Soluble in DMSO(Need ultrasonic) |
| Purity | ≥98% |
| Appearance | Light yellow to yellow Solid |
| Storage | Powder:2-8℃，2 years;Insolvent(Mother Liquid):-20℃，6 months;-80℃，1 year |
| MDL | MFCD11867705 |
| SMILES | CC(=O)OC1=CC2=C(S1)CCN(C2)C(C3=CC=CC=C3F)C(=O)C4CC4.Cl |
| InChIKey | JALHGCPDPSNJNY-UHFFFAOYSA-N |
| InChI | InChI=1S/C20H20FNO3S.ClH/c1-12(23)25-18-10-14-11-22(9-8-17(14)26-18)19(20(24)13-6-7-13)15-4-2-3-5-16(15)21;/h2-5，10，13，19H，6-9，11H2，1H3;1H |
| PubChem CID | 10158453 |
| Target Point | P2Y Receptor |
| Passage | GPCR & G Protein |
| Background | It is a potent P2Y12 receptor antagonist that inhibits ADP-induced platelet aggregation. |
| Biological Activity | Prasugrel Hydrochloride 是一种噻唑衍生物，是一种口服活性的 P2Y12 受体拮抗剂，也是一种血小板聚集抑制剂，可抑制 ADP 诱导的血小板聚集。[1-2] |
| Data Literature Source | [1]. Ogawa T，et al. Effects of prasugrel，a novel P2Y(12) inhibitor，in rat models of cerebral and peripheral artery occlusive diseases. Eur J Pharmacol. 2009 Jun 10;612(1-3):29-34. [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. |
| Unit | Bottle |
| Specification | 10mg 25mg |
Remark：These protocols are for reference only. Solarbio does not independently validate these methods.
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