Defluoro Prasugrel Hydrochloride

Product Name Defluoro Prasugrel Hydrochloride
Alternate Names Prasugrel Impurities, Impurities of Prasugrel
CAT No. CS-T-14782
CAS No. 1391053-53-4
Category Impurities
Stock IN-Stock
Mol. Wt. 391.91 g/mol
Mol. For. C₂₀H₂₂ClNO₃S
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Prasugrel
Therapeutic Anti-Thrombotics
Smileys CC(=O)OC1=CC2=C(S1)CCN(C2)C(C3=CC=CC=C3)C(=O)C4CC4.Cl
Canonical Smiles CC(=O)OC1=CC2=C(S1)CCN(C2)C(C3=CC=CC=C3)C(=O)C4CC4.Cl
InchIKey DMTWJXFEUBBGRR-UHFFFAOYSA-N
Inchl InChI=1S/C20H21NO3S.ClH/c1-13(22)24-18-11-16-12-21(10-9-17(16)25-18)19(20(23)15-7-8-15)14-5-3-2-4-6-14;/h2-6,11,15,19H,7-10,12H2,1H3;1H
IUPAC [5-(2-cyclopropyl-2-oxo-1-phenylethyl)-6,7-dihydro-4H-thieno[3,2-c]pyridin-2-yl] acetate;hydrochloride
Controlled No
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Defluoro Prasugrel Hydrochloride is a potent antiplatelet agent that inhibits platelet activation and aggregation. It is primarily used for the prevention of thrombotic events in patients with acute coronary syndrome who undergo a percutaneous coronary intervention (PCI) procedure. Defluoro Prasugrel Hydrochloride is a prodrug that requires hepatic metabolism to convert it into its active metabolite. Once activated, it irreversibly binds to the P2Y12 receptor on platelets, inhibiting their activation and subsequent aggregation. Defluoro Prasugrel Hydrochloride is administered orally as a tablet and is rapidly absorbed, reaching peak plasma concentrations within 30 minutes of ingestion. The drug has a half-life of approximately 7 hours and is primarily eliminated through the feces. The most common side effects associated with Defluoro Prasugrel Hydrochloride include bleeding, including gastrointestinal bleeding and bruising. Chemically, Defluoro Prasugrel Hydrochloride is an odorless, white to off-white powder that is freely soluble in water and methanol. Its chemical formula is C20H20FNO3S•HCl and its molecular weight is 409.9 g/mol. Defluoro Prasugrel Hydrochloride is a member of the thienopyridine class of antiplatelet agents and is structurally similar to clopidogrel and ticlopidine. However, it is more potent and has a faster onset of action compared to these agents.

Related Compounds

m-Fluoro Prasugrel Hydrochloride | Prasugrel Impurity of KSM-ll | Descyclopropyl-2-oxopropyl Prasugrel | Di-Acetyl Prasugrel HCl Impurity | Prasugrel Carboxyenone impurity | Prasugrel Impurity F | Prasugrel Endo iminium impurity | Prasugrel Impurity 39 | Prasugrel Impurity 25 | PRASUGREL 3-FLUORO IMPURITY | Prasugrel Impurity 29 | PRASUGREL 4-FLUORO IMPURITY | Prasugrel Hydroxy Thiolactone | Prasugrel EP Impurity F trifluoroacetate alt | Prasugrel cyclopropyl open ring impurity-1 | Prasugrel Impurity 19 | Prasugrel Impurity 4 | Desacetyl hydroxy prasugrel impurity | p-Fluoro Prasugrel Hydrochloride | Prasugrel Bromo Opened Ring Impurity | Bromo Prasugrel | Prasugrel Impurity 26 | Prasugrel Impurity 27 | Prasugrel cyclopropyl open ring impurity-2 |

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