PSB-0739,98.67%

产品编号:Bellancom-108660| CAS NO:1052087-90-7| 分子式:C26H17N3Na2O8S2| 分子量:609.54

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-108660
1300.00 杭州 北京(现货)
Bellancom-108660
2100.00 杭州 北京(现货)
Bellancom-108660
4500.00 杭州 北京(现货)
Bellancom-108660
7600.00 杭州 北京(现货)
Bellancom-108660
12000.00 杭州 北京(现货)

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PSB-0739

产品介绍 PSB-0739 是一种高亲和力、竞争性、非选择性的血小板 P2Y12 受体拮抗剂,Ki 值为 24.9 nM。P2Y12 受体在血小板聚集中起着至关重要的作用。PSB-0739 具有抗血栓作用。
生物活性

PSB-0739 is a high-affinity potent, competitive, nonselective platelet P2Y12 receptor antagonist with a Ki values of 24.9 nM. The P2Y12 receptor plays a crucial role in platelet aggregation. Antithrombotic effect.

体外研究

PSB-0739 is a potent competitive non-nucleotide antagonist at the human P2Y12 receptor with a pA2 value of 9.8.
PSB-0739 inhibits ADP-evoked Ca2+ responses with an EC50 of 5.4±1.8 μM and causes a rightward parallel shift in the ADP concentration–response curve in THP-1 cells.

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

Cell Viability Assay

Cell Line: THP-1 monocytic cell line
Concentration: 10 nM, 100 nM, 1 μM, 10 μM
Incubation Time:
Result: Attenuated ADP-evoked responses (IC50=5.4±1.8 μM).
体内研究
(In Vivo)

PSB-0739 (0.01-0.3 mg/kg, intrathecally) has dose-dependent and significant antihyperalgesic effect in low doses. The minimal effective dose (mED) is 0.1 mg/kg[4].

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

Animal Model: Male Wistar rats, 150-250 g, 6-8/group[4]
Dosage: 0.01, 0.03, 0.1, 0.3 mg/kg
Administration: Intrathecal injection ( i.t.)
Result: Displayed a dose-dependent inhibitory effect on mechanical hyperalgesia in the range of 0.01–0.1 mg/kg.
体内研究

PSB-0739 (0.01-0.3 mg/kg, intrathecally) has dose-dependent and significant antihyperalgesic effect in low doses. The minimal effective dose (mED) is 0.1 mg/kg[4].

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

Animal Model: Male Wistar rats, 150-250 g, 6-8/group[4]
Dosage: 0.01, 0.03, 0.1, 0.3 mg/kg
Administration: Intrathecal injection ( i.t.)
Result: Displayed a dose-dependent inhibitory effect on mechanical hyperalgesia in the range of 0.01–0.1 mg/kg.
体内研究

PSB-0739 (0.01-0.3 mg/kg, intrathecally) has dose-dependent and significant antihyperalgesic effect in low doses. The minimal effective dose (mED) is 0.1 mg/kg[4].

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

Animal Model: Male Wistar rats, 150-250 g, 6-8/group[4]
Dosage: 0.01, 0.03, 0.1, 0.3 mg/kg
Administration: Intrathecal injection ( i.t.)
Result: Displayed a dose-dependent inhibitory effect on mechanical hyperalgesia in the range of 0.01–0.1 mg/kg.
性状Solid
溶解性数据
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

参考文献

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