渗透剂(生化)
炎症体
体内
神经炎症
药理学
化学
神经科学
医学
心理学
生物
免疫学
炎症
生物技术
有机化学
作者
David Harrison,Andy Billinton,Mark G. Bock,Nicholas Clarke,Zsofia Digby,Christopher A. Gabel,Nicola Lindsay,Valérie Reader,Jane Scanlon,Pamela J. Smolak,Peter Thornton,Heather Wescott,Alan P. Watt
摘要
Inhibition of the NLRP3 inflammasome has emerged as a high potential treatment paradigm for the treatment of neuroinflammation, with demonstrated anti-neuroinflammatory effects in Parkinson's disease patients and a strong rationale in Alzheimer's disease and amyotrophic lateral sclerosis. To facilitate further progress in this field, brain penetrant NLRP3 inflammasome inhibitors as leads and tool compounds are required. We discovered a small molecule NLRP3 inflammasome inhibitor, NT-0527 (11), and extensively profiled this to reveal a highly potent, selective and brain penetrant compound. This was shown to be orally bioavailable, efficacious in an in vivo model of inflammation, and with good developability characteristics. However, NT-0527 exhibited CYP 2C19 time-dependent inhibition, which halted development, but this molecule could be employed as a valuable tool compound for the investigation of neuroinflammatory conditions where NLRP3 inflammasome activation is implicated.
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