Two pairs of diastereoisomeric isoflavone glucosides from the roots of Pueraria lobata

Fitoterapia. 2020 Jul:144:104594. doi: 10.1016/j.fitote.2020.104594. Epub 2020 Apr 14.

Abstract

Phytochemical investigation of the roots of Pueraria lobata led to the isolation of two pairs of new isoflavone glucosides, 3'-hydroxyneopuerarin A/B (1-2) and 3'-methoxyneopuerarin A/B (3-4). A pair of known compounds (5-6), which possess a very similar structure, were obtained together. Their structures were elucidated on the basis of spectroscopic data interpretation. Compounds 3-6 dose-dependently blocked the production of TNF-α and IL-6 in LPS-stimulated RAW264.7 cells, which indicated the potential anti-inflammatory effect of these compounds.

Keywords: Anti-inflammatory; C-glucofuranosyl; Isoflavone glucosides; Pueraria lobata.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / isolation & purification
  • Anti-Inflammatory Agents / pharmacology*
  • China
  • Glucosides / isolation & purification
  • Glucosides / pharmacology*
  • Interleukin-6 / metabolism
  • Isoflavones / isolation & purification
  • Isoflavones / pharmacology*
  • Mice
  • Molecular Structure
  • Phytochemicals / isolation & purification
  • Phytochemicals / pharmacology
  • Plant Roots / chemistry
  • Pueraria / chemistry*
  • RAW 264.7 Cells
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Anti-Inflammatory Agents
  • Glucosides
  • Interleukin-6
  • Isoflavones
  • Phytochemicals
  • Tumor Necrosis Factor-alpha
  • interleukin-6, mouse