Description
A reversible antagonist of P2Y12 (Ki = 23 nM); inhibits platelet aggregation in an hPRP assay (IC50 = 2.81 nM); inhibits thrombosis in a mouse model of vascular injury induced by FeCl3 at 60 mg/kg
Formal name: 5-chloro-N-[[[4-[6-fluoro-1,4-dihydro-7-(methylamino)-2,4-dioxo-3(2H)-quinazolinyl]phenyl]amino]carbonyl]-2-thiophenesulfonamide
Synonyms: PRT060128|PRT128
Molecular weight: 523.9
CAS: 936500-94-6
Purity: ≥98%
Formulation: A solid
Product Type|Biochemicals|Receptor Pharmacology|Antagonists||Research Area|Cardiovascular System|Blood|Coagulation & Hemostasis||Research Area|Cardiovascular System|Blood|Thrombosis