替卡格雷
化学
P2Y12
药理学
敌手
效力
血小板
血小板聚集
代谢物
血小板聚集抑制剂
受体
生物化学
体外
氯吡格雷
内科学
阿司匹林
医学
作者
Hao Zhang,Jun Li,Luyong Zhang,Ling‐Yi Kong,Hequan Yao,Hongbin Sun
标识
DOI:10.1016/j.bmcl.2012.04.050
摘要
Ticagrelor (1) is the first reversible P2Y12 receptor antagonist blocking adenine diphosphate (ADP)-induced platelet aggregation with rapid onset and offset of effects. In this study, synthesis of ticagrelor and its derivatives has been accomplished in a convergent way. The compound design was based on modifications of ticagrelor and its major metabolite (33) in order to ameliorate their pharmacokinetic properties and dosing profile. The final compounds (1a–g, 35a–g) were evaluated for their inhibitory effect on ADP-induced platelet aggregation in rats. The assay results showed that some compounds (e.g., 1b, 1d, 33, 35b, 35f) exhibited comparable potency with that of ticagrelor.
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