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Cangrelor
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Cangrelor图片
CAS NO:163706-06-7

AR-C69931MX
Cangrelor (AR-C69931MX) 是一种三磷酸腺苷类似物,是一种静脉注射的、可逆的且具有选择性的血小板P2Y12拮抗剂,具有迅速有效的抗血小板作用。Cangrelor 直接阻断腺苷二磷酸 (ADP) 诱导的血小板活化和聚集。Cangrelor 也是一种非特异性的GPR17拮抗剂。
生物活性

Cangrelor (AR-C69931MX), an adenosine triphosphate analogue, is an intravenous, reversible and selective plateletP2Y12antagonist, with prompt and potent antiplatelet effects. Cangrelor directly blocks adenosine diphosphate (ADP)-induced activation and aggregation of platelets. Cangrelor is also a nonspecificGPR17antagonist[1][2].

IC50& Target[1]

P2Y12 Receptor

 

体外研究
(In Vitro)

Cangrelor tetrasodium has pKbof 8.6-9.2 for hP2Y12 receptor[3].

体内研究
(In Vivo)

Cangrelor tetrasodium (10 mg/kg) not only significantly decreases BLM-induced release of inflammatory cytokines (PF4, CD40 L and MPO), but also decreases the increment of platelets, neutrophils and platelet-neutrophil aggregates in the fibrotic lung and in the peripheral blood of BLM-treated mice[2].

Clinical Trial
分子量

776.36

Formula

C17H25Cl2F3N5O12P3S2

CAS 号

163706-06-7

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

 
 
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