Design of iodinated radioligands for SPECT imaging of central human 5-HT4R using a ligand lipophilicity efficiency approach

Bioorg Chem. 2020 Mar:96:103582. doi: 10.1016/j.bioorg.2020.103582. Epub 2020 Jan 13.

Abstract

A series of iodinated ligands for the SPECT imaging of 5-HT4 receptors was designed starting from the previously reported hit MR-26132. We focused on the modulation of the piperidine-containing lateral chain by introducing hydrophilic groups in order to decrease the liphophilicity of the new ligands. All the synthesized compounds were tested for their binding affinities on 5-HT4Rs and based on the Ligand Lipophilicity Efficiency approach, compound 13 was further selected for radioiodination with iodine-125 and imaging experiments. Compound 13 showed its ability to displace the specific signal of the reference compound [125I]SB-207710 but no significant detection of [125I]13 was observed in vivo in SPECT experiments.

Keywords: 5-HT(4); LLE; Radio-iodination; SPECT imaging; Serotonin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain Chemistry
  • CHO Cells
  • Cricetulus
  • Dioxanes / chemistry
  • Humans
  • Iodine Radioisotopes / chemistry*
  • Ligands
  • Piperidines / chemistry*
  • Rats
  • Receptors, Serotonin, 5-HT4 / analysis*
  • Tomography, Emission-Computed, Single-Photon / methods*

Substances

  • Dioxanes
  • Iodine Radioisotopes
  • Ligands
  • Piperidines
  • SB 207710
  • Receptors, Serotonin, 5-HT4
  • piperidine
  • Iodine-125