(E)-5-styryl-1H-indole and (E)-6-styrylquinoline derivatives serve as probes for β-amyloid plaques

Molecules. 2012 Apr 10;17(4):4252-65. doi: 10.3390/molecules17044252.

Abstract

We report the synthesis and biological evaluation of novel (E)-5-styryl-1H-indole and (E)-6-styrylquinoline derivatives as probes for imaging β-amyloid (Aβ) plaques. These derivatives showed binding affinities for Aβ₁₋₄₀ aggregates with K(i) values varying from 4.1 to 288.4 nM. (E)-5-(4-iodostyryl)-1H-indole (8) clearly stained Aβ plaques in the brain sections of Alzheimer's disease (AD) model mice (APP/PS1). Furthermore, autoradiography for [¹²⁵I]8 displayed intense and specific labeling of Aβ plaques in the brain sections mentioned above with low background. In biodistribution experiments using normal mice [¹²⁵I]8 showed high initial brain uptake followed by rapid washout (4.27 and 0.64% ID/g at 2 and 30 min post injection, respectively). These findings suggests that [¹²³I]8 may be a potential SPECT imaging agent for detecting Aβ plaques in AD brain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / diagnostic imaging
  • Alzheimer Disease / metabolism
  • Amyloid beta-Peptides / metabolism
  • Animals
  • Autoradiography
  • Brain / pathology*
  • Female
  • Indoles* / chemistry
  • Indoles* / metabolism
  • Iodine Radioisotopes / metabolism
  • Mice
  • Mice, Transgenic
  • Molecular Probes* / chemistry
  • Molecular Probes* / metabolism
  • Plaque, Amyloid / diagnosis*
  • Plaque, Amyloid / metabolism
  • Protein Binding
  • Quinolines* / chemistry
  • Quinolines* / metabolism
  • Radionuclide Imaging
  • Staining and Labeling

Substances

  • Amyloid beta-Peptides
  • Indoles
  • Iodine Radioisotopes
  • Molecular Probes
  • Quinolines
  • styrylquinoline