Macrolide sesquiterpene pyridine alkaloids from Celastrus monospermus and evaluation of their immunosuppressive and anti-osteoclastogenesis activities

Bioorg Chem. 2024 Apr:145:107246. doi: 10.1016/j.bioorg.2024.107246. Epub 2024 Feb 27.

Abstract

Phytochemical investigation of the stems of Celastrus monospermus Roxb enabled isolation and identification of fifteen new macrolide sesquiterpene pyridine alkaloids (1-15) along with five known analogues. Their structures were elucidated by comprehensive spectroscopic analysis (NMR, HRESIMS, IR, UV), chemical hydrolysis, and single crystal X-ray diffraction analysis. Bioassay of the abundant isolates revealed that seven compounds inhibited the proliferation of B lymphocytes with IC50 values ranging between 1.4 and 19.9 μM. Among them, celasmondine C (3) could significantly promote the apoptosis of activated B lymphocyte, especially late-stage apoptosis. Besides, compounds 3, 16, and 20 exhibited potent suppression of osteoclast formation at a concentration of 1.0 μM. This investigation enriched the chemical diversity of macrolide sesquiterpene pyridine alkaloids, and supported evidence for the development of new immunosuppressive and anti-osteoclastogenesis agents.

Keywords: Anti-osteoclastogenesis; Celastrus monospermus Roxb; Immunosuppressive; Macrolide sesquiterpene pyridine alkaloid.

MeSH terms

  • Alkaloids* / chemistry
  • Alkaloids* / pharmacology
  • Celastrus* / chemistry
  • Macrolides
  • Molecular Structure
  • Pyridines / chemistry
  • Pyridines / pharmacology
  • Sesquiterpenes* / chemistry
  • Sesquiterpenes* / pharmacology

Substances

  • Macrolides
  • Pyridines
  • Alkaloids
  • Sesquiterpenes