1127252-92-9

Prasugrel-d<sub>5</sub> Chemical Structure
1127252-92-9

Chemical Structure

Prasugrel-d5

Synonym(s): PCR 4099-d5

  • CAS No.: 1127252-92-9
  • Formula:C20H15D5FNO3S
  • Molecular Weight:378.47

IUPAC Name: 5-(2-(cyclopropyl-d5)-1-(2-fluorophenyl)-2-oxoethyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridin-2-yl acetate

InChIKey: DTGLZDAWLRGWQN-GEXSZOTCSA-N

SMILES: FC1=CC=CC=C1C(N2CCC3=C(C=C(OC(C)=O)S3)C2)C(C4([2H])C([2H])([2H])C4([2H])[2H])=O

Biological Activity: Prasugrel-d5 is deuterium labeled Prasugrel. Prasugrel (PCR 4099), a thienopyridine and prodrug, inhibits platelet function. Prasugrel is an orally active and potent P2Y12 receptor antagonist, and inhibits ADP-induced platelet aggregation[1].

Cat. No. Product Name Purity Description Pricing
HY-15284S
Prasugrel-d5 Prasugrel-d5 is deuterium labeled Prasugrel. Prasugrel (PCR 4099), a thienopyridine and prodrug, inhibits platelet function. Prasugrel is an orally active and potent P2Y12 receptor antagonist, and inhibits ADP-induced platelet aggregation.
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HY-15284AR
Prasugrel hydrochloride (Standard) ≥98% Prasugrel (hydrochloride) (Standard) is the analytical standard of Prasugrel (hydrochloride). This product is intended for research and analytical applications. Prasugrel hydrochloride (PCR 4099 hydrochloride), a thienopyridine and proagent, inhibits platelet function. Prasugrel hydrochloride is an orally active and potent P2Y12 receptor antagonist, and inhibits ADP-induced platelet aggregation.
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HY-15284A
Prasugrel hydrochloride 98.49% Prasugrel hydrochloride (PCR 4099 hydrochloride), a thienopyridine and proagent, inhibits platelet function. Prasugrel hydrochloride is an orally active and potent P2Y12 receptor antagonist, and inhibits ADP-induced platelet aggregation.
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