化学
凝血病
盐酸盐
败血症
药理学
立体化学
生物化学
内科学
医学
作者
Hartmut Beck,Stefanie Mesch,Stefanie Zimmermann,Alexandros Vakalopoulos,Lutz Lehmann,Kersten M. Gericke,Frank Süßmeier,Lars Baerfacker,Alexander Hillisch,Katharina Meier,Adrian Tersteegen,Anja Buchmüller,Christoph Gerdes,Julia Dietze‐Torres,Elisabeth Kersten,Katrin Partikel,Andrew S. Brohl,Guillaume Levilain,Stefan Heitmeier,Nils Pfaff
标识
DOI:10.1021/acs.jmedchem.5c00538
摘要
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 (31), a potent and highly selective, direct dual FIIa/Xa inhibitor, with high solubility suited for i.v. 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 (t1/2), resulting in a high controllability of the pharmacological action.
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