Synthesis and pharmacological evaluation of benzannulated derivatives as potent and selective sigma-1 protein ligands - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue European Journal of Medicinal Chemistry Année : 2014

Synthesis and pharmacological evaluation of benzannulated derivatives as potent and selective sigma-1 protein ligands

Résumé

The σ1 proteins are considered to be a new class of target structures for several central nervous system disorders, including depression, anxiety, psychosis, and Parkinson's and Alzheimer's diseases. Recently, the involvement of these receptors in neuropathic pain and cancer has also been observed. So far, only a few ligands are in clinical trials. In a continuation of our previous studies on the development of σ1 ligands, a new series of benzannulated heterocycles was designed and synthesised. In vitro competition binding assays showed that many of them possessed high σ1 receptor affinity (Ki = 0.6–10.3 nM), and good σ2/σ1 subtype selectivity, without cytotoxic effects on SY5Y cells (human neuroblastoma cell line).
Fichier non déposé

Dates et versions

hal-02060851 , version 1 (07-03-2019)

Identifiants

Citer

Marion Donnier-Marechal, Pascal Carato, Delphine Le Broc, Christophe Furman, Patricia Melnyk. Synthesis and pharmacological evaluation of benzannulated derivatives as potent and selective sigma-1 protein ligands. European Journal of Medicinal Chemistry, 2014, ⟨10.1016/j.ejmech.2014.01.013⟩. ⟨hal-02060851⟩

Collections

UNIV-LILLE
11 Consultations
0 Téléchargements

Altmetric

Partager

Gmail Facebook X LinkedIn More