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J Med Chem ; 63(5): 2074-2094, 2020 03 12.
Article in English | MEDLINE | ID: mdl-31525963

ABSTRACT

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 IL1ß 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.


Subject(s)
Drug Delivery Systems/methods , Inflammatory Bowel Diseases/drug therapy , Inflammatory Bowel Diseases/metabolism , Purinergic P2X Receptor Antagonists/administration & dosage , Purinergic P2X Receptor Antagonists/metabolism , Receptors, Purinergic P2X7/metabolism , Animals , Cell Survival/drug effects , Cell Survival/physiology , Dextran Sulfate/toxicity , Female , HEK293 Cells , Humans , Inflammatory Bowel Diseases/chemically induced , Mice , Mice, Inbred C57BL
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