Synthesis and characterization of environment-sensitive fluorescent ligands for human 5-HT1A receptors with 1-arylpiperazine structure

J Med Chem. 2009 Dec 10;52(23):7892-6. doi: 10.1021/jm900706d.

Abstract

A series of "long-chain" 1-(2-methoxyphenyl)piperazine derivatives containing an environment-sensitive fluorescent moiety (4-amino-1,8-naphthalimide, 4-dimethylaminophthalimide, dansyl) was synthesized. The compounds displayed very high to moderate 5-HT(1A) receptor affinity and good fluorescence properties. 6-Amino-2-[5-[4-(2-methoxyphenyl)-1-piperazinyl]pentyl]-1H-benz[de]isoquinoline-1,3(2H)-dione (4) combined very high 5-HT(1A) receptor affinity (K(i) = 0.67 nM), high fluorescence emission in CHCl(3), and undetectable fluorescence emission in aqueous solution. It was evaluated for its ability to visualize 5-HT(1A) receptors overexpressed in CHO cells by fluorescence microscopy.

MeSH terms

  • Animals
  • Buffers
  • CHO Cells
  • Cell Membrane / metabolism
  • Cricetinae
  • Cricetulus
  • Drug Design
  • Fluorescent Dyes / chemical synthesis*
  • Fluorescent Dyes / chemistry
  • Fluorescent Dyes / metabolism*
  • Gene Expression Regulation
  • Humans
  • Methyl Chloride / chemistry
  • Microscopy, Fluorescence
  • Piperazines / chemical synthesis*
  • Piperazines / chemistry
  • Piperazines / metabolism*
  • Receptor, Serotonin, 5-HT1A / metabolism*

Substances

  • Buffers
  • Fluorescent Dyes
  • Piperazines
  • Receptor, Serotonin, 5-HT1A
  • Methyl Chloride