Prenylated Acylphloroglucinols from Hypericum jovis with Anti-inflammatory Potential

Planta Med. 2021 Nov;87(14):1184-1191. doi: 10.1055/a-1556-9721. Epub 2021 Aug 13.

Abstract

Thirteen prenylated acylphloroglucinols (1: -13: ), including 2 previously undescribed compounds (1: ) and (2: ), were isolated from Hypericum jovis. Their structures were elucidated by high-field NMR spectroscopy. The isolated prenylated acylphloroglucinols were evaluated for their anti-inflammatory effects in vitro through the reduction of the intercellular adhesion molecule 1 expression induced by TNF-α in the human microvascular endothelial cells 1 cell line. Compounds 3, 5, 6, 8,: and 12: significantly reduced intercellular adhesion molecule 1 expression in a concentration-dependent manner with IC50 values of 16.9, 34.4, 4.0, 3.2, and 7.7 µM, respectively. In addition, compound 12: showed notable inhibitory activity on the formation of cyclooxygenase-1- and 12-lipoxygenase-derived inflammatory mediators in an ex vivo cyclooxygenase-lipoxygenase assay. Eleven further constituents were isolated (14: -24: ), including the rare quercetin 3-O-(2-O-acetyl)-arabinofuranoside (18: ).

MeSH terms

  • Anti-Inflammatory Agents / pharmacology
  • Endothelial Cells
  • Hypericum*
  • Molecular Structure
  • Phloroglucinol / pharmacology
  • Prenylation

Substances

  • Anti-Inflammatory Agents
  • Phloroglucinol