Towards a Novel Class of Multitarget-Directed Ligands: Dual P2X7-NMDA Receptor Antagonists

Molecules. 2018 Jan 21;23(1):230. doi: 10.3390/molecules23010230.

Abstract

Multi-target-directed ligands (MTDLs) offer new hope for the treatment of multifactorial complex diseases such as Alzheimer's Disease (AD). Herein, we present compounds aimed at targeting the NMDA and the P2X7 receptors, which embody a different approach to AD therapy. On one hand, we are seeking to delay neurodegeneration targeting the glutamatergic NMDA receptors; on the other hand, we also aim to reduce neuroinflammation, targeting P2X7 receptors. Although the NMDA receptor is a widely recognized therapeutic target in treating AD, the P2X7 receptor remains largely unexplored for this purpose; therefore, the dual inhibitor presented herein-which is open to further optimization-represents the first member of a new class of MTDLs.

Keywords: Alzheimer’s disease; NMDA; P2X7; dual target compounds; neuroinflammation.

MeSH terms

  • Alzheimer Disease / drug therapy
  • Alzheimer Disease / metabolism
  • Cell Line, Tumor
  • Chemistry Techniques, Synthetic
  • Dose-Response Relationship, Drug
  • Drug Design
  • Drug Discovery
  • Humans
  • Inhibitory Concentration 50
  • Ligands
  • Molecular Structure
  • Purinergic P2X Receptor Antagonists / chemical synthesis
  • Purinergic P2X Receptor Antagonists / chemistry*
  • Purinergic P2X Receptor Antagonists / pharmacology*
  • Receptors, Purinergic P2X / chemistry*
  • Receptors, Purinergic P2X / metabolism

Substances

  • Ligands
  • Purinergic P2X Receptor Antagonists
  • Receptors, Purinergic P2X