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Hepatoprotective hemiterpene glycosides from the rhizome of Cibotium barometz (L.) J. Sm.

Abstract
Five previously undescribed hemiterpene glycosides, cibotiumbarosides E-I, and two known hemiterpene glucosides, were isolated from the rhizome of Cibotium barometz (L.) J. Sm. The structures of cibotiumbarosides E-I were established by 1D and 2D NMR spectroscopic analyses and HRMS. The absolute configuration of the aglycone of cibotiumbaroside E was assigned by calculated ECD with the TDDFT method. Cibotiumbarosides F and I both exhibited remarkable hepatoprotective activity against APAP-induced acute liver damage in vitro, which were more effective than the positive control, bicyclol. On the other hand, seven hemiterpene glycosides were all inactive in assays of cytotoxicity, neuroprotection, antidiabetes and anti-inflammation.
AuthorsMei-Ping Xie, Lan Li, Hua Sun, An-Qi Lu, Bo Zhang, Jian-Gong Shi, Dan Zhang, Su-Juan Wang
JournalPhytochemistry (Phytochemistry) Vol. 138 Pg. 128-133 (Jun 2017) ISSN: 1873-3700 [Electronic] England
PMID28262248 (Publication Type: Journal Article)
CopyrightCopyright © 2017 Elsevier Ltd. All rights reserved.
Chemical References
  • Glycosides
  • Hemiterpenes
  • Plant Extracts
Topics
  • Glycosides (chemistry, isolation & purification)
  • Hemiterpenes (chemistry, isolation & purification)
  • Hep G2 Cells
  • Humans
  • Molecular Structure
  • Plant Extracts (chemistry)
  • Rhizome (chemistry)
  • Tracheophyta (chemistry)

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