Structure elucidation of degradation products of Z-ligustilide by UPLC-QTOF-MS and NMR spectroscopy

Yao Xue Xue Bao. 2013 Jun;48(6):911-6.

Abstract

Z-Ligustilide, a major phthalide isolated from a widely used traditional Chinese medicine Ligusticum chuanxiong, possesses various pharmacological activities including neuroprotective, anti-inflammatory, antiproliferative and vasorelaxing effects. However, it is unstable and inclined to degrade in natural conditions, which limits its study and application greatly. In this study, degradation behavior of Z-ligustilide and its degradation products stored at room temperature under direct sunlight were investigated and structure elucidated by HPLC-UV, UPLC-QTOF-MS and NMR. Z-ligustilide degradation and total five degradation products were generated and detected. Two degradation products were unequivocally identified as senkyunolide I and senkyunolide H by comparison with reference compounds. Another two degradation products were further isolated by semi-preparative HPLC and structure elucidated as (E)-6, 7-trans-dihydroxyligustilide and (Z)-6, 7-epoxyligustilide by 1H and 13C NMR, respectively. The degradation pathways of Z-ligustilide were finally proposed. Oxidation, hydrolysis and isomerization are the major degradation reactions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Butyrolactone / analogs & derivatives*
  • 4-Butyrolactone / isolation & purification
  • 4-Butyrolactone / metabolism
  • Benzofurans / metabolism*
  • Chromatography, High Pressure Liquid
  • Hydrolysis
  • Ligusticum / chemistry
  • Magnetic Resonance Spectroscopy
  • Metabolic Networks and Pathways
  • Oxidation-Reduction
  • Plant Roots / chemistry
  • Plants, Medicinal / chemistry
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization

Substances

  • Benzofurans
  • senkyunolide H
  • senkyunolide I
  • ligustilide
  • 4-Butyrolactone