Discovery of novel benzofuran-based compounds with neuroprotective and immunomodulatory properties for Alzheimer's disease treatment

  • Eur J Med Chem. 2019 Sep 15:178:243-258. doi: 10.1016/j.ejmech.2019.05.080.
Serena Montanari  1 Ali Mokhtar Mahmoud  2 Letizia Pruccoli  3 Alessandro Rabbito  2 Marina Naldi  1 Sabrina Petralla  1 Ignacio Moraleda  4 Manuela Bartolini  1 Barbara Monti  1 Isabel Iriepa  5 Federica Belluti  1 Silvia Gobbi  1 Vincenzo Di Marzo  2 Alessandra Bisi  1 Andrea Tarozzi  3 Alessia Ligresti  2 Angela Rampa  6
Affiliations
  • 1. Department of Pharmacy and Biotechnology, Alma Mater Studiorum-University of Bologna, Via Belmeloro 6, 40126, Bologna, Italy.
  • 2. Endocannabinoid Research Group, Institute of Biomolecular Chemistry, National Research Council, Via Campi Flegrei 34, 80078, Pozzuoli, NA, Italy.
  • 3. Department for Life Quality Studies, Alma Mater Studiorum-University of Bologna, Corso d'Augusto 237, 47921, Rimini, Italy.
  • 4. Departamento de Química Orgánica y Química Inorgánica, Universidad de Alcalá, 28805, Alcalá de Henares, Madrid, Spain.
  • 5. Departamento de Química Orgánica y Química Inorgánica, Universidad de Alcalá, 28805, Alcalá de Henares, Madrid, Spain; Instituto de Investigación Química Andrés M. del Río (IQAR), Universidad de Alcalá, 28805, Alcalá de Henares, Madrid, Spain.
  • 6. Department of Pharmacy and Biotechnology, Alma Mater Studiorum-University of Bologna, Via Belmeloro 6, 40126, Bologna, Italy. Electronic address: [email protected].
Abstract

To address the multifactorial nature of Alzheimer's Disease (AD), a multi-target-directed ligand approach was herein developed. As a follow-up of our previous studies, a small library of newly designed 2-arylbenzofuran derivatives was evaluated towards cholinesterases and cannabinoid receptors. The two most promising compounds, 8 and 10, were then assessed for their neuroprotective activity and for their ability to modulate the microglial phenotype. Compound 8 emerged as able to fight AD from several directions: it restored the cholinergic system by inhibiting butyrylcholinesterase, showed neuroprotective activity against Aβ1-42 oligomers, was a potent and selective CB2 ligand and had immunomodulatory effects, switching microglia from the pro-inflammatory M1 to the neuroprotective M2 phenotype. Derivative 10 was a potent CB2 inverse agonist with promising immunomodulatory properties and could be considered as a tool for investigating the role of CB2 receptors and for developing potential immunomodulating drugs addressing the endocannabinoid system.

Keywords
Anti-inflammatory M2 phenotype; Aβ peptide; Benzofuran scaffold; CB receptors; MTDL; Neuroprotection.