Discovery of BAY 3389934 Hydrochloride: A Potent and Selective Small-Molecule Dual Factor IIa/Xa Inhibitor with Short Half-Life for the Acute Treatment of Sepsis-Induced Coagulopathy

Sepsis-induced coagulopathy (SIC) is a severe and frequent complication of sepsis, which is associated with high mortality in patients. So far, attempts have failed to establish a global standard of care in this difficult-to-treat indication. Anticoagulation with a dual inhibitor of the coagulation factors IIa (FIIa, thrombin) and Xa (FXa) has the potential to improve the treatment of life-threatening acute coagulation disorders, such as SIC. Herein, we describe the discovery of BAY 3389934 hydrochloride (<b>31</b>), a potent and highly selective, direct dual FIIa/Xa inhibitor, with high solubility suited for <i>i.v.</i> application. This small molecule acts as a metabolically soft active pharmaceutical ingredient (API) due to a labile carboxylic ester group, which is responsible for the desired short pharmacokinetic and pharmacological half-life (<i>t</i><sub>1/2</sub>), resulting in a high controllability of the pharmacological action.

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Journal
Journal of Medicinal Chemistry
Published
2025-06-11
DOI
https://doi.org/10.1021/acs.jmedchem.5c00538
Primary Topic
Blood Coagulation and Thrombosis Mechanisms
Type
article
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article

Discovery of BAY 3389934 Hydrochloride: A Potent and Selective Small-Molecule Dual Factor IIa/Xa Inhibitor with Short Half-Life for the Acute Treatment of Sepsis-Induced Coagulopathy

Lars Baerfacker, Stefan Heitmeier, Katharina Meier, Guillaume Levilain et al.
Journal of Medicinal Chemistry
Blood Coagulation and Thrombosis Mechanisms
article

Discovery of BAY 3389934 Hydrochloride: A Potent and Selective Small-Molecule Dual Factor IIa/Xa Inhibitor with Short Half-Life for the Acute Treatment of Sepsis-Induced Coagulopathy

Lars Baerfacker, Stefan Heitmeier, Katharina Meier, Guillaume Levilain, Julia Dietze‐Torres, Markus Follmann, Andrew Scott Brohl, Stefanie Zimmermann, Christoph Gerdes, Lutz Lehmann, Frank Süßmeier, Kersten M. Gericke, Elisabeth Kersten, Alexandros Vakalopoulos, Stefanie Mesch, Anja Buchmüller, Hartmut Beck, Adrian Tersteegen, Alexander Hillisch, Nils Pfaff, Katrin Partikel
article en

Abstract

Sepsis-induced coagulopathy (SIC) is a severe and frequent complication of sepsis, which is associated with high mortality in patients. So far, attempts have failed to establish a global standard of care in this difficult-to-treat indication. Anticoagulation with a dual inhibitor of the coagulation factors IIa (FIIa, thrombin) and Xa (FXa) has the potential to improve the treatment of life-threatening acute coagulation disorders, such as SIC. Herein, we describe the discovery of BAY 3389934 hydrochloride (<b>31</b>), a potent and highly selective, direct dual FIIa/Xa inhibitor, with high solubility suited for <i>i.v.</i> application. This small molecule acts as a metabolically soft active pharmaceutical ingredient (API) due to a labile carboxylic ester group, which is responsible for the desired short pharmacokinetic and pharmacological half-life (<i>t</i><sub>1/2</sub>), resulting in a high controllability of the pharmacological action.

Journal of Medicinal ChemistryVol. 68(12)
Roche (Switzerland) (CH), Sanofi (France) (FR), UCB Pharma (Germany) (DE), Bayer (Germany) (DE)
Openalex Percentile: Top 83%
Blood Coagulation and Thrombosis Mechanisms
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