抗血栓
化学
药理学
氯吡格雷
血小板
凝血酶
凝结
直接凝血酶抑制剂的发现与发展
受体
血栓形成
血小板活化
阿司匹林
医学
内科学
生物化学
作者
E. Scott Priestley,Jacques Banville,Daniel H. Deon,Laurence Dubé,Marc Gagnon,Julia Guy,Philippe Lapointe,Jean-François Lavallée,Alain Martel,Serge Plamondon,Roger Rémillard,Edward H. Ruediger,François Tremblay,Shana L. Posy,Victor R. Guarino,Jeremy M. Richter,Jianqing Li,Anuradha Gupta,Muthalagu Vetrichelvan,T. J. Balapragalathan
标识
DOI:10.1021/acs.jmedchem.2c00359
摘要
Protease-activated receptor 4 (PAR4) is a G-protein coupled receptor that is expressed on human platelets and activated by the coagulation enzyme thrombin. PAR4 plays a key role in blood coagulation, and its importance in pathological thrombosis has been increasingly recognized in recent years. Herein, we describe the optimization of a series of imidazothiadiazole PAR4 antagonists to a first-in-class clinical candidate, BMS-986120 (43), and a backup clinical candidate, BMS-986141 (49). Both compounds demonstrated excellent antithrombotic efficacy and minimal bleeding time prolongation in monkey models relative to the clinically important antiplatelet agent clopidogrel and provide a potential opportunity to improve the standard of care in the treatment of arterial thrombosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI