Development of Gleevec Analogues for Reducing Production of β-Amyloid Peptides through Shifting β-Cleavage of Amyloid Precursor Proteins. Academic Article uri icon

Overview

abstract

  • Imatinib mesylate, 1a, inhibits production of β-amyloid (Aβ) peptides both in cells and in animal models. It reduces both the β-secretase and γ-secretase cleavages of the amyloid precursor protein (APP) and mediates a synergistic effect, when combined with a β-secretase inhibitor, BACE IV. Toward developing more potent brain-permeable leads, we have synthesized and evaluated over 75 1a-analogues. Several compounds, including 2a-b and 3a-c, inhibited production of Aβ peptides with improved activity in cells. These compounds affected β-secretase cleavage of APP similarly to 1a. Compound 2a significantly reduced production of the Aβ42 peptide, when administered (100 mg/kg, twice daily by oral gavage) to 5 months old female mice for 5 days. A combination of compound 2a with BACE IV also reduced Aβ levels in cells, more than the additive effect of the two compounds. These results open a new avenue for developing treatments for Alzheimer's disease using 1a-analogues.

publication date

  • March 15, 2019

Research

keywords

  • Amyloid beta-Peptides
  • Amyloid beta-Protein Precursor
  • Antineoplastic Agents
  • Imatinib Mesylate

Identity

Scopus Document Identifier

  • 85063433212

Digital Object Identifier (DOI)

  • 10.1021/acs.jmedchem.8b02007

PubMed ID

  • 30873837

Additional Document Info

volume

  • 62

issue

  • 6