Metabolites of isocorynoxeine in rats after its oral administration

被引:7
|
作者
Chen, Ya-Ping [1 ,2 ]
Lu, Min-Nan [3 ]
Hao, Jing-Chao [1 ,2 ]
Li, Mei-Hong [1 ,2 ]
Hattori, Masao [4 ]
Wang, Wei [1 ,2 ,4 ]
机构
[1] Kunming Med Univ, Sch Pharmaceut Sci, Kunming 650500, Peoples R China
[2] Kunming Med Univ, Yunnan Prov Key Lab Pharmacol Nat Prod, Kunming 650500, Peoples R China
[3] Kunming Med Univ, Expt Ctr Med Sci Res, Kunming 650500, Peoples R China
[4] Toyama Univ, Inst Nat Med, Div Metab Engn, Sugitani, Toyama 2630, Japan
关键词
metabolites; isocorynoxeine; structure elucidation; CHROMATOGRAPHY-MASS-SPECTROMETRY; UNCARIA-RHYNCHOPHYLLA; LIQUID-CHROMATOGRAPHY; OXINDOLE ALKALOIDS; QUANTIFICATION; ISORHYNCHOPHYLLINE; IDENTIFICATION; TOMENTOSA; LEAVES; HOOKS;
D O I
10.1080/10286020.2014.1003182
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
This work presents the metabolites of isocorynoxeine (ICOR), which is one of four bioactive tetracyclic oxindole alkaloids isolated from Uncaria hooks used commonly in the traditional Chinese medicines and Kampo medicines. After oral administration of 40mgkg(-1) ICOR to rats, bile was drained and analyzed by LC-MS. Two phase I metabolites, namely 11-hydroxyisocorynoxeine (M1) and 10-hydroxyisocorynoxeine (M2), and two phase II metabolites, namely 11-hydroxyisocorynoxeine 11-O-beta-d-glucuronide (M3) and 10-hydroxyisocorynoxeine 10-O-beta-d-glucuronide (M4), were isolated from rat excreta and bile, respectively, whose structures were elucidated on the basis of CD, NMR, and MS.
引用
收藏
页码:384 / 390
页数:7
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