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Discovery of Milvexian, a High-Affinity, Orally Bioavailable Inhibitor of Factor XIa in Clinical Studies for Antithrombotic Therapy

Authors :
Karen A. Rossi
Ruth R. Wexler
Steven Sheriff
Dawn Sun
Jeffrey M. Bozarth
Jianqing Li
Elizabeth A. Dierks
James R. Corte
Yiming Wu
Donald J. P. Pinto
Silvi A. Chacko
Michael Galella
Joanna J. Zheng
Joseph E. Myers
Dauh-Rurng Wu
Tianan Fang
Joseph M. Luettgen
Pancras C. Wong
Xiaoping Hou
Pabbisetty Kumar Balashanmuga
Daniel Smith
Indawati De Lucca
Huiping Zhang
Wu Yang
Arvind Mathur
Yufeng Wang
Dilger Andrew K
William R. Ewing
Subramaniam Krishnananthan
Yeheng Zhu
Earl J. Crain
Theresa Ziemba
Source :
Journal of medicinal chemistry. 65(3)
Publication Year :
2021

Abstract

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.

Details

ISSN :
15204804
Volume :
65
Issue :
3
Database :
OpenAIRE
Journal :
Journal of medicinal chemistry
Accession number :
edsair.doi.dedup.....0bf4f1ea39b0f4f590f90003f6f693cc