Why the study?
Currently available FXa inhibitors carry a significant risk of life-threatening bleeding, creating an urgent unmet need for potent novel agents with a reduced bleeding risk.
This review outlines contemporary medicinal chemistry strategies for developing novel Factor Xa inhibitors that aim to maintain antithrombotic efficacy while reducing bleeding risk.
FXa inhibition merits continued antithrombotic drug development; leaves open clinical translation of next-generation agents.
Introduction: Thrombosis is a common causal pathology for stroke, acute coronary syndrome and venous thromboembolism disorders, which are the leading cause of death worldwide. Anticoagulants have exhibited a crucial role in the prevention and treatment of thrombotic diseases. Factor Xa (FXa) is a serine protease with a central role in activating the complex blood coagulation cascade, and it is therefore regarded as an attractive target for antithrombotic agents.Areas covered: The authors review the current status of medicinal chemistry strategies for the discovery of novel FXa inhibitors and provide their expert perspectives on their future development.Expert opinion: Even if only a number of small-molecule FXa inhibitors have been reported to date, all currently available FXa inhibitors are associated with significant risk of bleeding, which may become life-threatening. There is, therefore, an urgent and unmet demand for potent novel FXa inhibitors that are potent treatments for thrombotic disorders, but which have a reduced risk of bleeding if their use is to be increasingly favored.
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Hao et al. (2019) studied this question.
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