4.7 Article

Cytotoxic triterpenoid saponins from Lysimachia foenum-graecum

Journal

PHYTOCHEMISTRY
Volume 136, Issue -, Pages 165-174

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phytochem.2017.01.021

Keywords

Lysimachia foenum-graecum; Myrsinaceae; Triterpenoid saponins; Cytotoxic activities

Funding

  1. National Natural Science Foundation of China [21462006, 21431001]
  2. gs2:Ministry of Education of China [IRT_16R15]
  3. Natural Science Foundation of Guangxi [2014GXNSFBA118042, 2016GXNSFGA380005]
  4. Department of Education of Guangxi [ZD2014024]
  5. project of State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources, Ministry of Science and Technology of China [CMEMR2016-A02]
  6. Guangxi Normal University [2013ZD001]

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Eleven oleanane-type triterpenoid saponins, foegraecumosides A-K, and eight known ones, were isolated from the aerial parts of Lysimachia foenum-graecum. Their structures were elucidated by spectro-scopic data analyses and chemical methods. All isolated saponins were evaluated for their cytotoxicity against four human cancer cell lines (NCI-H460, MGC-803, HepG2, and T24). Seven saponins containing the aglycone cyclamiretin A exhibited moderate cytotoxicity against all tested human cancer cell lines, with IC50 values of 9.3-24.5 mu M. Simultaneously, the cytotoxic activities of foegraecumosides A and B, lysichriside A, ardisiacrispins A and B, cyclaminorin, and 3-O-alpha-L-rhamnopyranosyl-(1 -> 2)-beta-D-glucopyranosyl-(1 -> 4)-alpha-L-arabinopyranosyl-cyclamiretin A were tested on drug-resistant lung cancer cell lines (A549 and A549/CDDP, respectively). Ardisiacrispin B displayed moderate cytotoxicity against A549/CDDP, with an IC50 value of 8.7 mu M and a resistant factor (RF) of 0.9. (C) 2017 Elsevier Ltd. All rights reserved.

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