Three pairs of sesquiterpene enantiomers from Chloranthus multistachys pei

Nat Prod Res. 2022 Oct;36(20):5255-5262. doi: 10.1080/14786419.2021.1929974. Epub 2021 May 27.

Abstract

Phytochemical investigation on the whole plant of Chloranthus multistachys pei (Chloranthaceae) afforded three pairs of new sesquiterpene enantiomers (+)/(-)-chlorantene M [(+)/(-)-1], (+)/(-)-chlorantene M1 [(+)/(-)-2] and (+)/(-)-chlorantene N [(+)/(-)-3]. The structures of new compounds were determined through spectroscopic techniques (HR-ESI-MS, 1 D and 2 D NMR), besides, their absolute and relative configurations were established by using Single-crystal X-ray diffraction analysis and CD spectrum. The anti-inflammatory potential of all compounds was evaluated by applying LPS induced RAW 264.7 macrophage inflammatory model, and the results were that none of these compounds showed activity (IC50 > 100 μM).[Formula: see text].

Keywords: Chloranthus multistachys Pei; anti-inflammatory; enantiomer; sesquiterpene.

MeSH terms

  • Anti-Inflammatory Agents / chemistry
  • Anti-Inflammatory Agents / pharmacology
  • Lipopolysaccharides / pharmacology
  • Magnoliopsida* / chemistry
  • Molecular Structure
  • Phytochemicals
  • Sesquiterpenes* / chemistry
  • Sesquiterpenes* / pharmacology

Substances

  • Anti-Inflammatory Agents
  • Lipopolysaccharides
  • Phytochemicals
  • Sesquiterpenes