体内
芒果藤黄
化学
轨道轨道
黄原酮
硫酸化
代谢物
葡萄糖醛酸化
代谢途径
去甲基化
药理学
生物化学
羟基化
新陈代谢
生物
体外
立体化学
微粒体
色谱法
质谱法
医学
传统医学
酶
DNA甲基化
生物技术
基因表达
基因
作者
Fan Dong,Shaoping Wang,Ailin Yang,Haoran Li,Pingping Dong,Bing Wang,Long Dai,Yongqiang Lin,Jiayu Zhang
标识
DOI:10.2174/1389200222666211126093124
摘要
α-mangostin, a typical xanthone, often exists in Garcinia mangostana L. (Clusiaceae). α-mangostin was found to have a wide range of pharmacological properties. However, its specific metabolic route in vivo remains unclear, while these metabolites may accumulate to exert pharmacological effects, too.This study aimed to clarify the metabolic pathways of α-mangostin after oral administration to the rats.Here, an UHPLC-Q-Exactive Orbitrap MS was used for the detection of potential metabolites formed in vivo. A new strategy for the identification of unknown metabolites based on typical fragmentation routes was implemented.A total of 42 metabolites were detected, and their structures were tentatively identified in this study. The results showed that major in vivo metabolic pathways of α-mangostin in rats included methylation, demethylation, methoxylation, hydrogenation, dehydrogenation, hydroxylation, dehydroxylation, glucuronidation, and sulfation.This study is significant to expand our knowledge of the in vivo metabolism of α-mangostin and to understand the mechanism of action of α-mangostin in rats in vivo.
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