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PRASUGREL (C005B-313509)

Catalog No.
C005B-313509
Manufacturer No.
SML0331-10MG
Manufacturer Name
Sigma-Aldrich
Quantity
10
Unit of Measure
MG

Biochem/physiol Actions Prasugrel is a platelet inhibitor that reduces the aggregation of platelets by irreversible binding to P2Y12 receptors. Prasugrel interacts in an irreversible manner with the residues Cys97 and Cys175 of the human

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Biochem/physiol Actions

Prasugrel is a platelet inhibitor that reduces the aggregation of platelets by irreversible binding to P2Y12 receptors. Prasugrel interacts in an irreversible manner with the residues Cys97 and Cys175 of the human P2Y12-receptor.

Prasugrel is a thienopyridine prodrug and is considered to be more potent than clopidogrel. It shows a faster generation and also reduces thrombotic events. Prasugrel is less dependent on the CYP (cytochrome P450) enzymes for its conversion to active metabolite.

Features and Benefits

This compound is featured on the P2 Receptors: P2Y G-Protein Family page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

UPC:
42311524
Condition:
New
HazmatClass:
No
MPN:
SML0331-10MG
CAS:
150322-43-3

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