Synthesis and pharmacological evaluation of Tic-hydantoin derivatives as selective sigma1 ligands. Part 2

Bioorg Med Chem Lett. 2005 Nov 1;15(21):4828-32. doi: 10.1016/j.bmcl.2005.07.039.

Abstract

Herein is described a new class of selective sigma1 ligands consisting of tetrahydroisoquinoline-hydantoin (Tic-hydantoin) derivatives. Compound 1a has high affinity (IC50 = 16 nM) for sigma1 receptor and is selective in a large panel of therapeutic targets. This study presents structural changes on the side chain of the Tic-hydantoin core. Analogs of higher affinity could be identified (IC50 approximately 2-3 nM).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antidepressive Agents / chemical synthesis
  • Cell Survival / drug effects
  • Guinea Pigs
  • Hydantoins / chemical synthesis*
  • Hydantoins / pharmacology
  • Inhibitory Concentration 50
  • Ligands
  • Receptors, sigma / metabolism*
  • Structure-Activity Relationship

Substances

  • Antidepressive Agents
  • Hydantoins
  • Ligands
  • Receptors, sigma