生物活性 | |||
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靶点 |
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描述 | Cangrelor is the only currently available intravenous platelet P2Y12 receptor inhibitor, and its quick onset and offset make it an appealing option for antiplatelet therapy[1]. In vitro, the experiment focused on αIIbβ3 complex (platelet receptor for fibrinogen), and cangrelor (140μM, 15 min) suppressed the expression of this surface membrane activation marker in platelets[2]. 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[3]. |
临床研究 | |||||
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NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 |
NCT03182855 | Acute Coronary Syndrome ... 展开 >> Myocardial Infarction STEMI - ST Elevation Myocardial Infarction 收起 << | Phase 4 | Not yet recruiting | August 1, 2019 | Denmark ... 展开 >> Aarhus University Hospital Not yet recruiting Aarhus, Denmark, 8200 Contact: Jacob Thorsted Sorensen, MD, PhD +4540143563 jacsoe@rm.dk Contact: Steen D Kristensen, MD, DMSc +4530922336 stekrist@rm.dk 收起 << |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
1.16mL 0.23mL 0.12mL |
5.79mL 1.16mL 0.58mL |
11.57mL 2.31mL 1.16mL |
参考文献 |
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