CHRU de Lille, Faculté de Médecine-Pôle Recherche, Inserm U995, LIRIC, Université de Lille, Place Verdun, F-59045 Lille Cedex, France.
Yncréa Hauts-de-France, UCLille, Laboratoire de Pharmacochimie, Hautes Etudes d'Ingénieur (HEI), 13 rue de Toul, F-59046 Lille, France.
J Med Chem. 2020 Mar 12;63(5):2074-2094. doi: 10.1021/acs.jmedchem.9b00584. Epub 2019 Sep 27.
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 -P2X7 antagonist drug. Such a drug would raise the hope for a cure to many P2X7-dependent pathologies, including inflammatory, neurological, and immune diseases.
本报告涉及基于焦谷氨酸的 P2X7 拮抗剂的设计、合成和药理学评价。其中十几个被证明具有改善的性质,与参考拮抗剂 GSK1370319A 相比,它们在 BzATP 激活受体时抑制 YO-PRO-1/TO-PRO-3 的摄取和 IL1β 的释放,并减轻 DSS 诱导的结肠炎的迹象。通过对接研究和合成化合物的生物评价,突出了新的 SAR,并且本文所述焦谷氨酸的低毒性特征为寻找可用的-P2X7 拮抗剂药物提供了线索。这样的药物将为许多依赖 P2X7 的病理疾病的治疗带来希望,包括炎症、神经和免疫疾病。