Edoxaban 依度沙班; DU-176,99.59%

产品编号:Bellancom-10264| CAS NO:480449-70-5| 分子式:C24H30ClN7O4S| 分子量:548.06

Edoxaban(DU-176)是口服的FXa抑制剂,临床开发用于中风预防。

本网站销售的所有产品仅用于工业应用或者科学研究等非医疗目的,不可用于人类或动物的临床诊断或者治疗,非药用,非食用,

货号 包装 价格 库存与货期 购买量 操作
Bellancom-10264
500.00 杭州 北京(现货)
Bellancom-10264
700.00 杭州 北京(现货)
Bellancom-10264
1300.00 杭州 北京(现货)
Bellancom-10264
1800.00 杭州 北京(现货)

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Edoxaban 依度沙班; DU-176

产品介绍 Edoxaban (DU-176b) 是一种具有口服活性、高效、选择性和直接的 Factor Xa (FXa) 抑制剂,对人游离 FXa 和凝血酶原酶的 Ki 值分别为 0.561 nM 和 2.98 nM。Edoxaban 的选择性是其他凝血蛋白酶的 10000 倍以上。Edoxaban 可用于预防血栓栓塞性疾病的研究。
生物活性

Edoxaban (DU-176b) is an orally active, highly potent, selective, and direct Factor Xa (FXa) inhibitor with Ki values of 0.561 and 2.98 nM for free human FXa and prothrombinase. Edoxaban exhibits more than 10,000-fold selectivity over other coagulation proteases. Edoxaban can be used in preventing thromboembolic disease research.

体外研究

Edoxaban (1, 1 and 5 minutes respectively) prolongs PT,TT and APTT of human plasma in a concentration-dependent manner.
Edoxaban inhibits thrombin-induced platelet aggregation, with an IC50 of 2.90 µM.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay

Cell Line: Human, rat, cynomolgus monkey and rabbit plasma; Human platelet
Concentration:
Incubation Time: 1 and 5 minutes
Result: Antithrombin.
体内研究
(In Vivo)

Edoxaban (0.5, 2.5 and 12.5 mg/kg; p.o.; once) significantly and dose-dependently reduces the thrombus formation and prolongs PT.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male Slc: Wistar rats (210-240 g); Male New Zealand White rabbits(2.5-3.5 kg) (Both are venous stasis thrombosis model).
Dosage: 0.5, 2.5 and 12.5 mg/kg
Administration: Oral administration; once
Result: Inhibited exogenous FXa activity.
Antithrombotic.
体内研究

Edoxaban (0.5, 2.5 and 12.5 mg/kg; p.o.; once) significantly and dose-dependently reduces the thrombus formation and prolongs PT.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male Slc: Wistar rats (210-240 g); Male New Zealand White rabbits(2.5-3.5 kg) (Both are venous stasis thrombosis model).
Dosage: 0.5, 2.5 and 12.5 mg/kg
Administration: Oral administration; once
Result: Inhibited exogenous FXa activity.
Antithrombotic.
体内研究

Edoxaban (0.5, 2.5 and 12.5 mg/kg; p.o.; once) significantly and dose-dependently reduces the thrombus formation and prolongs PT.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male Slc: Wistar rats (210-240 g); Male New Zealand White rabbits(2.5-3.5 kg) (Both are venous stasis thrombosis model).
Dosage: 0.5, 2.5 and 12.5 mg/kg
Administration: Oral administration; once
Result: Inhibited exogenous FXa activity.
Antithrombotic.
性状Solid
溶解性数据
In Vitro: 

DMSO : 10 mg/mL (18.25 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 1.8246 mL 9.1231 mL 18.2462 mL
5 mM 0.3649 mL 1.8246 mL 3.6492 mL
10 mM 0.1825 mL 0.9123 mL 1.8246 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
参考文献

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