CAS NO: | 503612-47-3 |
生物活性 | Apixaban (BMS-562247-01) is a highly selective, reversible and orally active inhibitor ofFactor XawithKiof 0.08 nM and 0.17 nM in human and rabbit, respectively[1]. Apixaban is in development for the prevention and treatment of various thromboembolic diseases[2]. | ||||||||||||||||
IC50& Target | IC50: 0.08 nM (Human Factor Xa), 0.17 nM (Rabbit Factor Xa) | ||||||||||||||||
体外研究 (In Vitro) | Apixaban (BMS-562247-01) prolongs the clotting times of normal human plasma with the concentrations (EC2x) of 3.6 μM, 0.37 μM, 7.4 μM, and 0.4 μM, which are required respectively to double the prothrombin time (PT), modified prothrombin time (mPT), activated partial thromboplastin time (APTT) and HepTest. Besides, Apixaban shows the highest potency in human and rabbit plasma, but less potency in rat and dog plasma in both the PT and APTT assays[2]. | ||||||||||||||||
体内研究 (In Vivo) | Apixaban (BMS-562247-01) shows the excellent pharmacokinetics with very low clearance (Cl: 0.02 L/kg/h), and low volume of distribution (Vdss: 0.2 L/kg) in the dogs. Besides, Apixaban also exhibits a moderate half-life (T1/2: 5.8 hours) and good oral bioavailability (F: 58%)[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 459.50 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C25H25N5O4 | ||||||||||||||||
CAS 号 | 503612-47-3 | ||||||||||||||||
中文名称 | 阿哌沙班 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 50 mg/mL(108.81 mM;Need ultrasonic) H2O :< 0.1 mg/mL(insoluble) 配制储备液
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