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,Arvind Mathur,Ji Hua,Mario Callejo,Jocelyne Guay,Chi Shing Sum,Mary Ellen Cvijic,Carol A. Watson,Pancras C. Wong,Jing Yang,Michel Bouvier,David A. Gordon,Ruth R. Wexler,Anne Marinier
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.