Pyroglutamide-Based P2X7 Receptor Antagonists Targeting Inflammatory Bowel Disease
- Creators
- Homerin, Germain
- Baudelet, Davy
- Dufrénoy, Pierrick
- Rigo, Benoît
- Millet, Régis
- Dezitter, Xavier
- Furman, Christophe
- Ragé, Guillaume
- Lipka, Emmanuelle
- Farce, Amaury
- Renault, Nicolas
- Sendid, Boualem
- Jawhara, Samir
- Charlet, Rogatien
- Leroy, Jordan
- Phanithavong, Mélodie
- Richeval, Camille
- Wiart, Jean-François
- Allorge, Delphine
- Adriouch, Sahil
- Vouret-Craviari, Valérie
- Ghinet, Alina
- Others:
- Institute for Translational Research in Inflammation - U 1286 (INFINITE (Ex-Liric)) ; Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)
- Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)
- Physiopathologie et biothérapies des maladies inflammatoires et autoimmunes ; Université de Rouen Normandie (UNIROUEN) ; Normandie Université (NU)-Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM)
- Institut de Recherche sur le Cancer et le Vieillissement (IRCAN) ; Université Nice Sophia Antipolis (1965 - 2019) (UNS) ; COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Côte d'Azur (UCA)
- Alexandru Ioan Cuza University of Iași [Romania]
Description
This report deals with the design, the synthesis, and the pharmacological evaluation of pyroglutamide-based P2X7 antagonists. A dozen were shown to possess improved properties, among which inhibition of YO-PRO-1/TO-PRO-3 uptake and IL1β release upon BzATP activation of the receptor and dampening signs of DSS-induced colitis on mice, in comparison with reference antagonist GSK1370319A. Docking study and biological evaluation of synthesized compounds has highlighted new SAR, and low toxicity profiles of pyroglutamides herein described are clues for the finding of a usable h-P2X7 antagonist drug. Such a drug would raise the hope for a cure to many P2X7-dependent pathologies, including inflammatory, neurological, and immune diseases.
Abstract
International audience
Additional details
- URL
- https://hal.archives-ouvertes.fr/hal-03093950
- URN
- urn:oai:HAL:hal-03093950v1
- Origin repository
- UNICA