267
Views
4
CrossRef citations to date
0
Altmetric
Original Articles

Bioactive phenolic acid-substituted glycoses and glycosides from rhizomes of Cibotium barometz

, , , , , & show all
Pages 947-953 | Received 06 Nov 2018, Accepted 20 Dec 2018, Published online: 29 Jan 2019
 

Abstract

Two rarely phenolic acid-substituted alloses (1, 2) and one new glucoside (3), as well as nine known compounds (4–12) were isolated from rhizomes of Cibotium barometz (L.) J. Sm. Structures of 1–3 were established by extensively spectroscopic analyses (NMR, MS, etc.) and acid hydrolysis. All compounds were evaluated for the hepatoprotective activities against APAP-induced HepG2 cell damage. Compounds 1, 47, 10 exhibited significant hepatoprotective activities, even more strongly than positive control, bicycol. In addition, compounds 1 and 9 could reduce PC12 cell death induced by serum deprivation.

Acknowledgments

The authors greatly thank Prof. Xiaoguang Chen (cytotoxicity), Prof. Naihong Chen (neuroprotection), Prof Fei Ye (XOD), and Prof Qi Hou (anti-inflammation) for conducting the bioassay experiments.

Disclosure statement

The authors declare that they have no competing interests.

Additional information

Funding

This work was financially supported by the CAMS Innovation Fund for Medical Sciences (CIFMS) No. 2016-I2M-3-011.

Log in via your institution

Log in to Taylor & Francis Online

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 61.00 Add to cart

Issue Purchase

  • 30 days online access to complete issue
  • Article PDFs can be downloaded
  • Article PDFs can be printed
USD 426.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.