凝血酶
直接凝血酶抑制剂的发现与发展
达比加群
凝血酶生成
医学
药理学
血栓形成
重症监护医学
化学
华法林
内科学
心房颤动
血小板
作者
Jiangming Wang,Xiaojing Sun,Na Li,Ruilong Sheng,Ruihua Guo
标识
DOI:10.2174/0929867329666220906105200
摘要
Thrombosis is one of the most important pathogenic factors related to cardiovascular diseases. Presently, thrombin inhibitors have gradually gained prominence in clinical practice due to their unique potential, such as dabigatran. Nevertheless, the risk of bleeding is not completely eliminated, and the threats of gastrointestinal bleeding are even increased in some cases. Therefore, developing new oral thrombin inhibitors with low side effects is urgent. In this paper, we summarized recent advances in the newly synthesized and isolated thrombin inhibitors from 2000 to 2019 and their structure-activity relationships (SARs) along with structure-dependent pharmacokinetic parameters, guiding the next generation of oral thrombin inhibitors.
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