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Synthesis and biological evaluation of two salidroside analogues in the PC12 cell model exposed to hypoglycemia and serum limitation.

Abstract
Salidroside is a phenylpropanoid glycoside isolated from Rhodiola rosea L., a traditional Chinese medicinal plant, and has displayed a broad spectrum of pharmacological properties. In this paper, two analogues were prepared with the glucosamine and N-acetylglucosamine as glycosyl donor, 2-(4-hydroxyphenyl)ethanol as glycosyl acceptor. The effects of them over PC12 cell model exposed to hypoglycemia and serum limitation were assessed with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, Flow Cytometry and Western blot analysis.
AuthorsYibing Guo, Xiaohong Li, Yahong Zhao, Yongxing Si, Hui Zhu, Yumin Yang
JournalChemical & pharmaceutical bulletin (Chem Pharm Bull (Tokyo)) Vol. 59 Issue 8 Pg. 1045-7 ( 2011) ISSN: 1347-5223 [Electronic] Japan
PMID21804252 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Glucosides
  • Phenols
  • rhodioloside
Topics
  • Animals
  • Apoptosis (drug effects)
  • Glucosides (chemical synthesis, chemistry, pharmacology)
  • Hypoglycemia (metabolism)
  • PC12 Cells
  • Phenols (chemical synthesis, chemistry, pharmacology)
  • Rats
  • Rhodiola (chemistry)
  • Serum (metabolism)

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