Tranexamic acid-d2-1 is a deuterated form of tranexamic acid, an antifibrinolytic agent that inhibits the binding of plasmin and elastase-derived plasminogen fragments to lysine-binding sites, with an IC50 of 5 mM. This stable isotope is particularly useful in pharmacokinetic studies and metabolic research where precise quantification of drug metabolism and disposition is required. Its application in research extends to understanding coagulation disorders and therapeutic drug monitoring.
Tranexamic acid-d2-1 is a deuterated form of tranexamic acid, an antifibrinolytic agent that inhibits the binding of plasmin and elastase-derived plasminogen fragments to lysine-binding sites, with an IC50 of 5 mM. This stable isotope is particularly useful in pharmacokinetic studies and metabolic research where precise quantification of drug metabolism and disposition is required. Its application in research extends to understanding coagulation disorders and therapeutic drug monitoring.
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