Family · Pharmaceutical analytical standards
Nafamostat
A synthetic serine protease inhibitor developed in Japan, where it has been approved since 1986 for pancreatitis and since 1989 for disseminated intravascular coagulation and as an anticoagulant during dialysis. This family brings together the active ingredient, labelled standards and other impurities.
Did you know?Its half-life is about 8 minutes and dialysis itself removes it: so its anticoagulant effect stays concentrated almost entirely in the external circuit.
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Custom synthesis of impurities, metabolites and labelled compounds, with the same characterisation level.
