Parallel synthesis of a series of subtype-selective NMDA receptor antagonists

Bioorg Med Chem Lett. 2000 Mar 20;10(6):527-9. doi: 10.1016/s0960-894x(00)00035-4.

Abstract

A series of 1-(heteroarylthioalkyl)-4-benzylpiperidines was rapidly synthesized through the use of parallel synthesis to investigate the binding affinity for the NR1A/2B receptor subtype.

MeSH terms

  • Animals
  • Excitatory Amino Acid Antagonists / chemical synthesis*
  • Excitatory Amino Acid Antagonists / pharmacology
  • Oxidopamine
  • Piperidines / chemical synthesis*
  • Piperidines / pharmacology
  • Rats
  • Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors*
  • Structure-Activity Relationship
  • Sympathectomy, Chemical
  • Sympatholytics

Substances

  • Excitatory Amino Acid Antagonists
  • Piperidines
  • Receptors, N-Methyl-D-Aspartate
  • Sympatholytics
  • Oxidopamine