[A new styrene dimer derivative from Litsea greenmaniana]

Zhongguo Zhong Yao Za Zhi. 2017 Mar;42(5):912-914. doi: 10.19540/j.cnki.cjcmm.20170122.001.
[Article in Chinese]

Abstract

A new styrene dimer derivative has been isolated from the branch of Litsea greenmaniana by column chromatography over silica gel and Sephadex LH-20, as well as semi-preparative HPLC. Its structure was identified by spectroscopic data analysis (MS, UV, IR, 1D and 2D NMR) as (E)-2,4-bis(p-hydroxyphenyl)-2-butenol, named as listeanol. At a concentration of 1×10-5 mol•L⁻¹, compound 1 was inactive in the assays, including cytotoxicity against human tumor cell lines (HCT-8, Bel-7402, BGC-823, A549 and A2780), antioxidant activity in Fe²⁺-cystine-induced rat liver microsomal lipid peroxidation, neuroprotective activity against serum deprivation or glutamate induced neurotoxicity in cultures of PC12 cells, and the inhibitory activity against protein tyrosine phosphatase 1B (PTP1B).

Keywords: Litsea greenmaniana; chemical constituents; styrene dimer derivative.

MeSH terms

  • Animals
  • Antineoplastic Agents, Phytogenic
  • Antioxidants
  • Cell Line, Tumor
  • Chromatography, High Pressure Liquid
  • Humans
  • Lipid Peroxidation
  • Litsea / chemistry*
  • Microsomes, Liver / drug effects
  • Molecular Structure
  • Neuroprotective Agents
  • PC12 Cells
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1 / antagonists & inhibitors
  • Rats
  • Styrenes / isolation & purification*

Substances

  • Antineoplastic Agents, Phytogenic
  • Antioxidants
  • Neuroprotective Agents
  • Styrenes
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1