Flocoumafen (WL 108366) is an orally active vitamin K epoxide reductase inhibitor and a multi-target ligand, which includes prostaglandin F synthase, serum albumin, glucocorticoid receptor 2, and MMP-9. Flocoumafen is a second-generation anticoagulant rodenticide (ARs) with a half-life of 177.4 hours and has deadly anticoagulant effects[1][2][3].
Molecular Weight:
542.54
Purity:
99.17
CAS Number:
[90035-08-8]
Formula:
C33H25F3O4
Target:
Glucocorticoid Receptor,MMP,VKOR
Application Notes:
MCE Product type: Reference compound
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