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Description: Dicoumarol (also named as Dicumarol) is an oral and competitive inhibitor of NAD(P)H:quinone oxidoreductase 1 (NQO1) and PDK1 with IC50s of 0.37 and 19.42 uM, respectively. It is used as an anticoagulant by interfering with the metabolism of vitamin K. Dicoumarol is a naturally occurring anticoagulant that functions as a functional vitamin K depleter, similar to warfarin, a drug that dicoumarol inspired. It is also used in biochemical experiments as an inhibitor of reductases. Like all 4-hydroxycoumarin drugs it is a competitive inhibitor of vitamin K epoxide reductase, an enzyme that recycles vitamin K, thus causing depletion of active vitamin K in blood.
References: J Biol Chem. 2006 Dec 8; 281(49):37416-26; Clin Cancer Res. 2004 Jul 1; 10(13):4550-8.
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All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.
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