代谢途径
葡萄糖醛酸化
香豆素
羟基化
硫酸化
化学
代谢组学
东莨菪碱
新陈代谢
葡萄糖醛酸
去甲基化
生物化学
体内
代谢物
色谱法
体外
生物
微粒体
有机化学
酶
DNA甲基化
替代医学
生物技术
基因表达
病理
基因
医学
作者
Yao Xiao,Yikun Wang,Xue‐Rong Xiao,Qi Zhao,Jianfeng Huang,Weifeng Zhu,Fei Li
出处
期刊:Xenobiotica
[Taylor & Francis]
日期:2020-03-16
卷期号:50 (9): 1076-1089
被引量:29
标识
DOI:10.1080/00498254.2020.1744047
摘要
Coumarins have aroused high interests due to their diverse bioactivities. Understanding of its metabolism contributes to determine the druggability of coumarin in vivo.A sensitive and efficient strategy based on ultra-performance liquid chromatography-mass spectrometer (UPLC-MS) analysis combined with various data-processing techniques including metabolomics and multiple mass defect filter (MMDF) was established for the comprehensive screening and elucidation of potential coumarin metabolites.Total 20 metabolites of scoparone were identified in this study, including 14 undescribed metabolites. The metabolism of two other similar coumarins scopoletin and esculetin also could be determined using this strategy.By the established strategy, this study gives the insights about the major metabolic pathways of scoparone in vivo and in vitro metabolism, including demethylation, hydroxylation, hydration, cysteine conjugation, glucuronide conjugation and sulfate conjugation. Additionally, the metabolic pathways of scopoletin and esculetin were determined as hydroxylation, glucuronidation and sulfation. These results contribute to the understanding of metabolic characterization of coumarins, and demonstrate that the combination of UPLC-MS-based metabolomics and MMDF is a powerful approach to determine the metabolic pathways of coumarin compounds.
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