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.
Profile of NT-0527, a brain penetrant NLRP3 Inflammasome inhibitor suitable as an in vivo tool compound for neuroinflammatory disorders.
NT-0527 是一种可穿透血脑屏障的 NLRP3 炎症小体抑制剂,适用于作为神经炎症性疾病的体内治疗药物
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作者:Harrison David, Billinton Andy, Bock Mark G, Clarke Nicholas P, Digby Zsofia, Gabel Christopher A, Lindsay Nicola, Reader Valérie, Scanlon Jane, Smolak Pamela, Thornton Peter, Wescott Heather, Watt Alan P
| 期刊: | RSC Medicinal Chemistry | 影响因子: | 3.600 |
| 时间: | 2025 | 起止号: | 2025 Sep 4 |
| doi: | 10.1039/d5md00639b | 研究方向: | 神经科学 |
| 信号通路: | 炎性小体 | ||
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