Betrixaban (PRT054021) hydrochloride is a highly potent, selective, and orally efficaciousfactor Xa(fXa) inhibitor with anIC₅₀of 1.5 nM. Betrixaban hydrochloride shows antithrombotic effect^[1][3].

IC₅₀: 1.5 nM (fXa)^[1]
K_i: 0.117 nM (fXa), 1.8 μM (hERG)^[1]

Betrixaban (PRT054021) shows IC₅₀of 8.9 μM in patch clamp hERG assays^[1].
Betrixaban shows an IC₅₀and a K_iof 6.3 μM and 3.5 μM for the plasma kallikrein, respectively^[1].
Betrixaban (hERG K_i1.8 μM) exhibits significantly lower hERG activity than all the others (hERG K_i?0.5 μM)^[1].
Betrixaban (5-25 ng/mL) inhibits thrombin generation^[3].

Betrixaban (0.5 mg/kg, i.v.; 2.5 mg/kg, p.o.) has bioavailability of 51.6% in dog^[1].
Betrixaban (0.75 mg/kg, i.v.; 7.5 mg/kg, p.o.) has bioavailability of 58.7% in monkey^[1].
Betrixaban mediated whole-blood INR increase is reversed by r-Antidote. After i.v. infusion for 30 min, the total plasma concentrations of Betrixaban is 0.2±0.01 μM, and the percentages of unbound inhibitor is 40%±7.2%. After administration of r-Antidote, the total plasma concentration increased to 2.0±0.4 μM, and the percentage of unbound inhibitor declined to 0.3%±0.1%^[2].
Betrixaban (3 mg/kg) shows nearly comparable inhibition of thrombus mass to enoxaparin 1.6 mg/kg (76% vs 96% inhibition) in the rabbit abdominal vena cava model of clot accretion on cotton threads^[3].
Betrixaban (19.1 mg/kg) is at least as effective at maintaining patency as enoxaparin 7.6 mg/kg and clopidogrel 3 mg/kg/d (90% vs 70% vs 80% patency, respectively) in the ferric chloride injury model of rodent carotid artery^[3].

488.37

C₂₃H₂₃Cl₂N₅O₃

2099719-47-6

贝曲西班盐酸盐

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