Metabolic characterization of meso-dihydroguaiaretic acid in liver microsomes and in mice.

Food and Chemical Toxicology(2015)

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摘要
•MDGA is rapidly metabolized by CYP and UGT in HLMs and MLMs.•Extensive metabolism causes poor bioavailability of MDGA in mice.•MDGA exhibits selective CYP2E1 inhibitory activity in HLMs.•MDGA-induced CYP2E1 inhibition is competitive.
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关键词
meso-Dihydroguaiaretic acid,Metabolic stability,Pharmacokinetics,CYP inhibition,CYP2E1
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