[CAS NO. 389574-19-0]  Prasugrelhydrochloride

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PRODUCTS SPECIFICATIONS [389574-19-0]

Catalog
HY-15284A
Brand
MCE
CAS
389574-19-0

DESCRIPTION [389574-19-0]

Overview

MDLMFCD11867705
Molecular Weight409.90
Molecular FormulaC20H21ClFNO3S
SMILESFC1=CC=CC=C1C(C(C2CC2)=O)N3CCC4=C(C3)C=C(S4)OC(C)=O.Cl

For research use only. We do not sell to patients.

Summary

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


IC50 & Target

P2Y12 receptor [1]


In Vivo

In rat platelets, Prasugrel hydrochloride active metabolite inhibits in vitro platelet aggregation induced by adenosine ADP (10μM) with an IC 50 value of 1.8 μM [2] .
Prasugrel hydrochloride acts faster and is significantly more potent than Clopidogrel in vivo. Prasugrel hydrochloride is an inactive prodrug that requires metabolic processing in vivo to generate the active antiplatelet metabolite. Prasugrel hydrochloride is rapidly absorbed from the gut. After oral administration of standard-loading doses of 60 mg, maximum plasma levels of the active metabolite are achieved within 1 h, effective, maximum inhibition of platelet aggregation at 1-2 h [1] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.


Clinical Trial

NCT Number Sponsor Condition Start Date Phase
NCT01700322 Johannes Gutenberg University Mainz
Coronary Artery Disease
August 2012 Phase 4
NCT03454841 Collegium Medicum w Bydgoszczy
Acute Myocardial Infarction
February 26, 2018
NCT01135667 Lene Holmvang|Rigshospitalet, Denmark
Coronary Artery Disease|Percutaneous Coronary Intervention|Acute Coronary Syndromes
September 2010 Phase 4

Appearance

Solid


Shipping

Room temperature in continental US; may vary elsewhere.


Storage

4°C, sealed storage, away from moisture and light

* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)


Solvent & Solubility

In Vitro:

DMSO : 41.67 mg/mL ( 101.66 mM ; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.4396 mL 12.1981 mL 24.3962 mL
5 mM 0.4879 mL 2.4396 mL 4.8792 mL
10 mM 0.2440 mL 1.2198 mL 2.4396 mL
* Please refer to the solubility information to select the appropriate solvent.
In Vivo:
  • 1.

    Add each solvent one by one: 10% DMSO >> 40% PEG300 >> 5% Tween-80 >> 45% saline

    Solubility: ≥ 2.08 mg/mL (5.07 mM); Clear solution

  • 2.

    Add each solvent one by one: 10% DMSO >> 90% (20% SBE-β-CD in saline)

    Solubility: ≥ 2.08 mg/mL (5.07 mM); Clear solution

  • 3.

    Add each solvent one by one: 10% DMSO >> 90% corn oil

    Solubility: ≥ 2.08 mg/mL (5.07 mM); Clear solution

* All of the co-solvents are available by MCE.


Synonyms

Ethanone, 2-[2-(acetyloxy)-6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl]-1-cyclopropyl-2-(2-fluorophenyl)-, hydrochloride (1:1)
Ethanone, 2-[2-(acetyloxy)-6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl]-1-cyclopropyl-2-(2-fluorophenyl)-, hydrochloride
Prasugrel hydrochloride
2-Acetoxy-5-(α-cyclopropylcarbonyl-2-fluorobenzyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride
Prasu Doc
Efient
Effient