Metabolic characterization of meso-dihydroguaiaretic acid in liver microsomes and in mice.
Food and Chemical Toxicology(2015)
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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