Quantitative determination and pharmacokinetic study of the novel anti-Parkinson's disease candidate drug FLZ in rat brain by high performance liquid chromatography–tandem mass spectrometry-Reference-Cited by-同舟云学术

Quantitative determination and pharmacokinetic study of the novel anti-Parkinson's disease candidate drug FLZ in rat brain by high performance liquid chromatography–tandem mass spectrometry

Published:2012-07 Issue: Volume:66 Page:232-239
ISSN:0731-7085
Container-title:Journal of Pharmaceutical and Biomedical Analysis
language:en
Short-container-title:Journal of Pharmaceutical and Biomedical Analysis

Author:

Hou Jinfeng,Qu Feng,Wu Caisheng,Ren Qiang,Zhang Jinlan

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry

Reference28 articles.

1. Synthesis and antioxiactivity of squamosamide cycnc analogs;Xie;Acta Acad. Med. Sin.,2004

2. The novel squamosamide derivative (compound FLZ) attenuated 1-methyl, 4-phenyl-pyridinium ion (MPP+)-induced apoptosis and alternations of related signal transduction in SH-SY5Y cells;Zhang;Neuropharmacology,2007

3. Pharmacological study of the novel compound FLZ against experimental Parkinson's models and its active mechanism;Feng;Mol. Neurobiol.,2005

4. The novel squamosamide derivative FLZ protects against 6-hydroxydopamine-induced apoptosis through inhibition of related signal transduction in SH-SY5Y cells;Zhang;Eur. J. Pharmacol.,2007

5. FLZ, a novel HSP27 and HSP70 inducer, protects SH-SY5Y cells from apoptosis caused by MPP(+);Kong;Brain Res.,2011

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