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Prasugrel

Prasugrel Structure
CAS No.
150322-43-3
Chemical Name:
Prasugrel
Synonyms
Effient;Prasugrel base;Efient;CS-1997;Prasita;Ly640315;Ly 640315;Prasugrel;Ly-640315;prasugren
CBNumber:
CB01463424
Molecular Formula:
C20H20FNO3S
Molecular Weight:
373.44
MOL File:
150322-43-3.mol
Modify Date:
2024/5/22 13:49:24

Prasugrel Properties

Melting point 120.0 to 124.0 °C
Boiling point 493.5±45.0 °C(Predicted)
Density 1.347
storage temp. 2-8°C
solubility DMSO: >5mg/mL (warmed at 60 °C)
pka 3.65±0.20(Predicted)
form powder
color white to beige
InChIKey DTGLZDAWLRGWQN-UHFFFAOYSA-N
CAS DataBase Reference 150322-43-3(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Safety Statements  24/25
WGK Germany  3
HS Code  29349990

Prasugrel price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) SML0331 Prasugrel ≥98% (HPLC) 150322-43-3 10MG ₹11268.83 2022-06-14 Buy
Sigma-Aldrich(India) SML0331 Prasugrel ≥98% (HPLC) 150322-43-3 50MG ₹45010.35 2022-06-14 Buy
TCI Chemicals (India) P2040 Prasugrel 150322-43-3 200MG ₹7700 2022-05-26 Buy
Product number Packaging Price Buy
SML0331 10MG ₹11268.83 Buy
SML0331 50MG ₹45010.35 Buy
P2040 200MG ₹7700 Buy

Prasugrel Chemical Properties,Uses,Production

Description

Prasugrel is a third-generation thienopyridine that has been developed and launched for the prevention of atherothrombotic events in patients with ACS or following PCI. While the second-generation agent clopidogrel was an improvement over the first-generation ticlopidine, which suffered from gastrointestinal adverse effects and the risk of neutropenia with prolonged use, its delayed onset of action and considerable interpatient variability prompted the search for the next-generation thienopyridine. The mechanism of action of these platelet inhibitors involves initial biological activation to a sulfhydryl metabolite that irreversibly binds to the P2γ12 receptor on platelets via disulfide formation, thereby preventing platelet activation and aggregation by the endogenous agonist adenosine diphosphate (ADP). The advantage of prasugrel over its predecessors is its more efficient and consistent absorption and rapid conversion to its active metabolite. Co-administration of thienopyridines with acetylsalicylic acid (aspirin), an inhibitor of the synthesis of the platelet aggregation mediator thromboxane A2, is an effective antiplatelet strategy and joins antagonists of glycoprotein IIb/IIIa, which target the final step in platelet aggregation, in the medical arsenal combating atherothrombotic events.

Uses

Prasugrel is a platelet inhibitor that reduces aggregation of platelets by being a P2Y12(ADP receptor) inhibitor.

Clinical Use

Prasugrel is a platelet inhibitor developed by Daiichi Sankyo Co. and is marketed in the United States in cooperation with Eli Lilly and Company for acute coronary syndromes planned for percutaneous coronary intervention (PCI). Prasugrel was approved for use in Europe in February 2009, and is currently available in the UK. In the U.S. prasugrel is also approved for the reduction of thrombotic cardiovascular events, including stent thrombosis, in patients with acute coronary syndrome who are to be managed with PCI. Prasugrel is a member of the thienopyridine class of ADP receptor inhibitors, and irreversibly binds to P2Y12 receptors.

Side effects

In addition to the hemorrhagic side effect, other serious adverse events included AF, bradycardia, leucopenia, severe thrombocytopenia, angiodema, anemia, and abnormal hepatic function with hypertension, headache, back pain, dyspnea, nausea, dizziness, and diarrhea as less severe complaints. Prasugrel is contraindicated in patients with active pathological bleeding, such as peptic ulcers or intracranial hemorrhage, and in patients with a history of prior transient ischemic attack or stroke. In addition, in patients 75 years old, <60 kg, or likely to undergo urgent coronary artery bypass graft surgery, the risk may not outweigh the benefit. When possible, prasugrel treatment should be discontinued at least 7 days prior to any surgery. While warfarin and non-steroidal antiinflammatory drugs (NSAIDS) may increase the risk of bleeding with coadministration of prasugrel, no drug interactions are anticipated with concomitant use of drugs that are inducers or inhibitors of the cytochrome P450 enzymes. Prasugrel may also be administered with aspirin (75-325 mg per day), heparin, GP IIb/IIIa inhibitors, statins, digoxin, and drugs that elevate gastric pH, including PPIs and H2 blockers.

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Prasugrel Spectrum

Prasugrel 2-[2-(Acetyloxy)-6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl]-1-cyclopropyl-2-(2-fluorophenyl)ethanone Ethanone, 2-(2-(acetyloxy)-6,7-dihydrothieno(3,2-C)pyridin-5(4H)-yl)-1-cyclopropyl-2-(2-fluorophenyl)- Ly 640315 Ly640315 Ly-640315 Unii-34K66tbt99 5-(2-cyclopropyl-1-(2-fluorophenyl)-2-oxoethyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridin-2-yl acetate prasugrel, 2-[2-(Acetyloxy)-6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl]-1-cyclopropyl-2-(2-fluorophenyl)ethanone Prasugrel(Effient) Prasugrel  5-[(1S)-2-cyclopropyl-1-(2-fluorophenyl)-2-oxoethyl]-4H,5H,6H,7H-thieno[3,2-c]pyridin-2-yl acetate Prasugrel(CS-747) 2-Acetoxy-5-(a-cyclopropylcarbonyl-2-flurobenzyl)-4,5,6,7-tetrahydrothieno [3,2-c]pyridine CS-1997 EFFIENT; EFIENT; PRASITA Prasita prasugren Prasugrel> Prasugrel USP/EP/BP Prasugrel (PCR 4099 Prasugrel impurities1177 PrasugrelQ: What is Prasugrel Q: What is the CAS Number of Prasugrel Q: What is the storage condition of Prasugrel TIANFU-CHEM---Prasugrel Efient Prasugrel base Effient Plague Ray 150322-43-3 LUVOX