Research and Development, Bristol Myers Squibb Company, P.O. Box 5400, Princeton, New Jersey 08543, United States.
J Med Chem. 2022 Feb 10;65(3):1770-1785. doi: 10.1021/acs.jmedchem.1c00613. Epub 2021 Sep 8.
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. 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 (, , FXIa = 0.11 nM) as a clinical candidate for the prevention and treatment of thromboembolic disorders, suitable for oral administration.
因子 XIa (FXIa) 是凝血级联反应中的一种酶,被认为可以放大凝血酶的生成,但在止血中作用有限。从临床前模型和人类遗传学来看,FXIa 的抑制剂有可能成为一种具有卓越疗效和安全性的抗血栓药物。可逆和不可逆的 FXIa 抑制剂在动物模型中表现出了优异的抗血栓疗效,且出血时间无延长(Weitz, J. I., Chan, N. C. 2019, 39 (1), 7-12)。在此,我们报告了一类新型含吡唑 P2' 部分的大环 FXIa 抑制剂的发现。通过优化该系列化合物的药代动力学 (PK) 特性、游离分数和溶解度,确定了 (,, FXIa = 0.11 nM) 作为预防和治疗血栓栓塞性疾病的临床候选药物,适合口服给药。