The synthesis and SAR of 2-arylsulfanylphenyl-1-oxyalkylamino acids as GlyT-1 inhibitors

Bioorg Med Chem Lett. 2006 Aug 1;16(15):3981-4. doi: 10.1016/j.bmcl.2006.05.017. Epub 2006 May 24.

Abstract

Elevation of glycine levels by inhibition of the glycine transporter-1 (GlyT-1) and activation of the NMDA receptor is a potential strategy for the treatment of schizophrenia. A novel series of 2-arylsulfanylphenyl-1-oxyalkyl amino acids have been identified. The most prominent member of this series S-1-{2-[3-(3-fluoro-phenylsulfanyl)biphenyl-4-yloxy]ethyl}pyrrolidine-2-carboxylic acid (38) is a potent GlyT-1 inhibitor (IC50=59 nM). In vitro and in vivo assessment of CNS exposure indicates this compound is a likely substrate for active efflux transporters.

MeSH terms

  • Amino Acids / chemical synthesis*
  • Amino Acids / chemistry
  • Amino Acids / pharmacokinetics
  • Amino Acids / pharmacology*
  • Blood-Brain Barrier
  • Caco-2 Cells
  • Glycine Plasma Membrane Transport Proteins / antagonists & inhibitors*
  • Humans
  • Structure-Activity Relationship

Substances

  • Amino Acids
  • Glycine Plasma Membrane Transport Proteins