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405940-76-3

CAS 405940-76-3
分子式 C24H21ClF4N8O2
分子量 564.923
MOL 文件 405940-76-3.mol
405940-76-3 結(jié)構(gòu)式 405940-76-3 結(jié)構(gòu)式

常見(jiàn)問(wèn)題列表

生物活性
Razaxaban hydrochloride (BMS 561389 hydrochloride) 是一種高效,選擇性和口服活性的 factor Xa 抑制劑,Ki 為 0.19 nM。Razaxaban hydrochloride 對(duì) factor Xa 的選擇性優(yōu)于其他相關(guān)絲氨酸蛋白酶 (> 5000 倍)。Razaxaban hydrochloride 也是一種有效的凝血酶抑制劑,Ki 為 540 nM。Razaxaban hydrochloride 具有很強(qiáng)的抗血栓形成活性。
靶點(diǎn)

Ki: 0.19 nM (Factor Xa); 540 nM (Thrombin)

體外研究

Razaxaban (compound 11d) shows good Caco-2 permeability.
The anticoagulant activity of Razaxaban (compound 11d) is evaluated in the in vitro human plasma activated partial thromboplastin time (aPTT) and human prothrombin time (PT) assays. Razaxaban shows a doubling of aPTT and PT at 6.1 μM and 2.1 μM, respectively. The human and rabbit plasma protein binding are found to be 90.5% and 93.4%, respectively, using equilibrium dialysis. Razaxaban is found to have similar affinity in the rabbit factor Xa assay with a K i of 0.16 nM.

體內(nèi)研究

Razaxaban (Compound 11d; 0.21-9.4 mg/kg/hour; intravenous injection) inhibits thrombus formation in a dose-dependent manner with an ID 50 of 1.6 μmol/kg/h in the rabbit arterio-venous shunt thrombosis model.

Animal Model: Rabbit arterio-venous shunt thrombosis model
Dosage: 0.21 mg/kg/hour, 0.7 mg/kg/hour, 2.1 mg/kg/hour, 9.4 mg/kg/hour
Administration: Intravenous injection
Result: Inhibited thrombus formation in a dose-dependent manner with an ID 50 of 1.6 μmol/kg/h.
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