Cytotoxic biflavones from Stellera chamaejasme

Fitoterapia. 2014 Dec:99:334-40. doi: 10.1016/j.fitote.2014.10.002. Epub 2014 Oct 12.

Abstract

Bioassay-guided phytochemical studies on Stellera chamaejasme led to the isolation of two new biflavones, chamaejasmenin E (1) and chamaejasmin D (2), together with ten known compounds. The structures of new compounds were elucidated by extensive spectroscopic analyses and their absolute configurations on 2, 3, 2″ and 3″ were confirmed by TDDFT quantum chemical calculated ECD spectra combined with experimental ECD spectra. All isolated biflavones were evaluated for their cytotoxic activities against Bel-7402 and A549 tumor cell lines, and sikokianin D (3) was found to possess the most potential cytotoxic activities against both the two cell lines with IC50 values of 1.29 ± 0.21 and 0.75 ± 0.25 μM, respectively. Moreover, some structure-function relationships of these bioflavones for cytotoxic activities were explored and summarized.

Keywords: Chamaejasmenin E; Chamaejasmin D; Cytotoxic activity; ECD; Stellera chamaejasme.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biflavonoids / chemistry
  • Biflavonoids / isolation & purification
  • Cell Line, Tumor
  • Flavones / chemistry*
  • Flavones / isolation & purification
  • Humans
  • Molecular Structure
  • Plant Roots / chemistry
  • Structure-Activity Relationship
  • Thymelaeaceae / chemistry*

Substances

  • Biflavonoids
  • Flavones
  • chamaejasmenin E
  • chamaejasmin D