化学
一氧化氮
噻氯匹定
药理学
血小板
血小板聚集
二磷酸腺苷
体外
生物化学
有机化学
氯吡格雷
内科学
阿司匹林
医学
作者
Xiaoli Wang,Linna Wang,Zhangjian Huang,Xiao Sheng,Tingting Li,Hui Ji,Jinyi Xu,Yihua Zhang
标识
DOI:10.1016/j.bmcl.2013.02.035
摘要
A series of novel nitric oxide releasing derivatives of 6-amino-3-n-butylphthalide were designed, synthesized and evaluated as potential antiplatelet agents. Compound 10b significantly inhibited the adenosine diphosphate (ADP)-induced platelet aggregation in vitro, superior to 6-amino-3-n-butylphthalide, 3-n-butylphthalide (NBP) and ticlopidine. Meanwhile 10b released moderate levels of NO, which could be beneficial for improving cardiovascular and cerebral circulation. Furthermore, 10b had an enhanced aqueous solubility relative to NBP. These findings may provide new insights into the development of novel antiplatelet agents for the treatment of thrombosis-related ischemic stroke.
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