Flocoumafen is an orally active vitamin K epoxide reductase inhibitor that functions primarily as an anticoagulant rodenticide. Its mechanism involves a prolonged inhibition of blood coagulation, leading to effective rodent control. In addition to its primary target, Flocoumafen interacts with several other proteins, including prostaglandin F synthase and the glucocorticoid receptor 2. This second-generation anticoagulant displays a half-life of 177.4 hours, contributing to its lethal efficacy against rodent populations.
Flocoumafen is an orally active vitamin K epoxide reductase inhibitor that functions primarily as an anticoagulant rodenticide. Its mechanism involves a prolonged inhibition of blood coagulation, leading to effective rodent control. In addition to its primary target, Flocoumafen interacts with several other proteins, including prostaglandin F synthase and the glucocorticoid receptor 2. This second-generation anticoagulant displays a half-life of 177.4 hours, contributing to its lethal efficacy against rodent populations.
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