Darexaban (YM150) is a potent, selective and orally active factor Xa (FXa) inhibitor with an IC 50 of 54.6 nM. Darexaban shows high selectivity against other related serine proteases, such as trypsin, thrombin , and kallikrein. Darexaban has anticoagulant and antithrombotic effects . In Vitro Darexaban is an oral direct factor Xa (FXa) inhibitor that is rapidly and extensively metabolized into its glucuronide conjugate (YM-222714) post-administration. Darexaban competitively and selectively inhibits human FXa, and also inhibits the prothrombin activation induced by prothrombinase complex or whole blood clot with similar potency to free FXa. MCE has not independently confirmed the accuracy of these methods. They are for reference only. In Vivo In mice, Darexaban inhibits FXa activity in plasma with an ED 50 value of 24.8 mg/kg. Darexaban prolonges prothrombin time (PT) at 3 mg/kg. In a pulmonary thromboembolism (PE) mouse model, Darexaban dose-dependently reduces the mortality rate, significantly so at 10 mg/kg. In a FeCl3-induced venous thrombosis (VT) mouse model, Darexaban (0.3-10 mg/kg) dose-dependently decreases the thrombus protein content, significantly so at doses of 3 mg/kg or higher. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid
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Darexaban
CAS number：365462-23-3 molecular formula：C27H30N4O4
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| Chinese alias | 达雷沙班 | ||
| English alias | BS-46688 | DTXSID101030146 | KF322K101S | AKOS040751402 | Tanexaban [INN] | N-[2-HYDROXY-6-(4-METHOXYBENZAMIDO)PHENYL]-4-(4-METHYL-1,4-DIAZEPAN-1-YL)BENZAMIDE | AT18264 | DAREXABAN [WHO-DD] | UNII-KF322K101S | Tanexaban | N-(3-Hydroxy-2-(4-(4-methyl-1,4-d | ||
| CAS number | 365462-23-3 | molecular formula | C27H30N4O4 |
| molecular weight | 474.6 g/mol | Exact mass | ≥99% |
| PSA | 94.100 Ų | logp | 3.5 |
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