Metabolites of isocorynoxeine in rats after its oral administration-Reference-Cited by-同舟云学术

Metabolites of isocorynoxeine in rats after its oral administration

Published:2015-01-30 Issue:4 Volume:17 Page:384-390
ISSN:1028-6020
Container-title:Journal of Asian Natural Products Research
language:en
Short-container-title:Journal of Asian Natural Products Research

Author:

Chen Ya-Ping¹,Lu Min-Nan²,Hao Jing-Chao¹,Li Mei-Hong¹,Hattori Masao³,Wang Wei¹³

Affiliation:

1. School of Pharmaceutical Sciences and Yunnan Provincial Key Laboratory of Pharmacology for Natural Products, Kunming Medical University, Kunming 650500, China

2. Experiment Center for Medical Science Research, Kunming Medical University, Kunming 650500, China

3. Division of Metabolic Engineering, Institute of Natural Medicine, University of Toyama, Sugitani 2630, Japan

Publisher

Informa UK Limited

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,General Medicine,Analytical Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10286020.2014.1003182

Reference17 articles.

1. Evaluation of the Protective Effects of Alkaloids Isolated from the Hooks and Stems of Uncaria sinensis on Glutamate-induced Neuronal Death in Cultured Cerebellar Granule Cells from Rats

2. Suppressive effects of isorhynchophylline on 5-HT2A receptor function in the brain: Behavioural and electrophysiological studies

3. Alkaloids from the Leaves of Uncaria rhynchophylla and Their Inhibitory Activity on NO Production in Lipopolysaccharide-Activated Microglia

4. The Blood–Brain Barrier Permeability of Geissoschizine Methyl Ether in Uncaria Hook, a Galenical Constituent of the Traditional Japanese Medicine Yokukansan

5. DETERMINATION OF ISOCORYNOXEINE IN RAT PLASMA BY LIQUID CHROMATOGRAPHY MASS SPECTROMETRY AND ITS APPLICATION

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3. Endothelium-independent vasodilator effect of isocorynoxeine in vitro isolated from the hook of Uncaria rhynchophylla (Miquel);Naunyn-Schmiedeberg's Archives of Pharmacology;2018-08-02

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5. Bioreduction of the C C double bond with Pseudomonas monteilii ZMU-T17: one approach to 3-monosubstituted oxindoles;Tetrahedron;2016-06