Isolation and biomimetic synthesis of anti-inflammatory stilbenolignans from Gnetum cleistostachyum

Chem Pharm Bull (Tokyo). 2006 Jul;54(7):1053-7. doi: 10.1248/cpb.54.1053.

Abstract

One new stilbenolignan, gnetucleistol F (1), and four known stilbenolignans, gnetofuran A (2), lehmbachol D (3), gnetifolin F (4) and gnetumontanin C (5) were isolated from the lianas of Gnetum cleistostachyum C. Y. CHENG (Gnetaceae). Their structures and relative configurations were determined by means of spectroscopic evidence. Compounds 1, 2, 3 and 4 were synthesized for the first time on the basis of their biogenetic pathway, and their possible biomimetical synthetic mechanisms were discussed. The pharmacological activities of all stilbenolignans have been tested. Among them, 1, 2, 3, 4 and 5 showed moderate inhibitory activities on TNF-alpha and 1 also showed potent inhibitory activity on malondialdehyde.

MeSH terms

  • Anti-Inflammatory Agents / chemical synthesis*
  • Anti-Inflammatory Agents / isolation & purification
  • Anti-Inflammatory Agents / pharmacology
  • Gnetum / chemistry*
  • Inhibitory Concentration 50
  • Lignans / chemical synthesis*
  • Lignans / isolation & purification
  • Lignans / pharmacology
  • Magnetic Resonance Spectroscopy
  • Malondialdehyde / antagonists & inhibitors
  • Molecular Structure
  • Stilbenes / chemical synthesis*
  • Stilbenes / isolation & purification
  • Stilbenes / pharmacology
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors
  • Tumor Necrosis Factor-alpha / drug effects

Substances

  • Anti-Inflammatory Agents
  • Lignans
  • Stilbenes
  • Tumor Necrosis Factor-alpha
  • Malondialdehyde