抗血栓
化学
生物利用度
药理学
药代动力学
止血
凝结
纤溶剂
直接凝血酶抑制剂的发现与发展
口服
凝血酶
医学
内科学
血小板
作者
Andrew K. Dilger,Kumar B. Pabbisetty,James R. Corte,Indawati De Lucca,Tianan Fang,Wu Yang,Donald Pinto,Yufeng Wang,Yeheng Zhu,Arvind Mathur,Jianqing Li,Xiaoping Hou,Daniel Smith,Dawn Sun,Huiping Zhang,Subramaniam Krishnananthan,Dauh‐Rurng Wu,Joseph E. Myers,S. Sheriff,Karen A. Rossi
标识
DOI:10.1021/acs.jmedchem.1c00613
摘要
Factor XIa (FXIa) is an enzyme in the coagulation cascade thought to amplify thrombin generation but has a limited role in hemostasis. From preclinical models and human genetics, an inhibitor of FXIa has the potential to be an antithrombotic agent with superior efficacy and safety. Reversible and irreversible inhibitors of FXIa have demonstrated excellent antithrombotic efficacy without increased bleeding time in animal models (Weitz, J. I., Chan, N. C. Arterioscler. Thromb. Vasc. Biol. 2019, 39 (1), 7−12). Herein, we report the discovery of a novel series of macrocyclic FXIa inhibitors containing a pyrazole P2′ moiety. Optimization of the series for (pharmacokinetic) PK properties, free fraction, and solubility resulted in the identification of milvexian (BMS-986177/JNJ-70033093, 17, FXIa Ki = 0.11 nM) as a clinical candidate for the prevention and treatment of thromboembolic disorders, suitable for oral administration.
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