Synthetic phenylethanoid glycoside derivatives as potent neuroprotective agents

Eur J Med Chem. 2015 May 5:95:313-23. doi: 10.1016/j.ejmech.2015.03.038. Epub 2015 Mar 18.

Abstract

Several phenylethanoid glycoside derivatives were designed and synthesized. Most of the synthetic compounds showed significant neuroprotective effects, including antioxidative and anti-apoptotic properties. Specifically, target compounds displayed potent effects against various toxicities such as H2O2 and 6-hydroxydopamine (6-OHDA) in PC12 cells. Among the synthetic derivatives, three compounds (5, 6, 8) exhibited much superior activities to the marketed drug Edaravone. The compounds were able to prevent the 6-OHDA-induced damage in PC12 cells in a dose-dependent manner. The anti-apoptotic effects could be observed via cell morphological changes. Moreover, the compounds significantly reduced the intracellular ROS increase resulting from 6-OHDA treatment. The preliminary structure-activity relationships were also explored. Compounds 5, 6, 8 may hold the potential as promising neuroprotective agents and new lead compounds for the treatment of neurodegenerative diseases or cerebral ischemia.

Keywords: Anti-apoptosis; Antioxidant; Neuroprotective agent; Phenylethanoid glycoside; Structure modification.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood-Brain Barrier / metabolism
  • Cell Survival / drug effects
  • Chemistry Techniques, Synthetic
  • Drug Design*
  • Free Radical Scavengers / chemical synthesis
  • Free Radical Scavengers / chemistry*
  • Free Radical Scavengers / metabolism
  • Free Radical Scavengers / pharmacology*
  • Glycosides / chemical synthesis
  • Glycosides / chemistry*
  • Glycosides / metabolism
  • Glycosides / pharmacology*
  • Neuroprotective Agents / chemical synthesis
  • Neuroprotective Agents / chemistry*
  • Neuroprotective Agents / metabolism
  • Neuroprotective Agents / pharmacology*
  • PC12 Cells
  • Permeability
  • Rats
  • Structure-Activity Relationship

Substances

  • Free Radical Scavengers
  • Glycosides
  • Neuroprotective Agents