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
NodThera Ltd. Suite 8, The Mansion, Chesterford Research Park, Little Chesterford, Saffron Walden Essex CB10 1XL UK
NodThera Inc. P.O. Box 156, Suite 1702, 265 Franklin Street Boston MA 02110 USA.
RSC Med Chem. 2025 Sep 4. doi: 10.1039/d5md00639b.
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 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.
抑制NLRP3炎性小体已成为治疗神经炎症的一种极具潜力的治疗模式,在帕金森病患者中已显示出抗神经炎症作用,在阿尔茨海默病和肌萎缩侧索硬化症中也有充分的理论依据。为推动该领域的进一步发展,需要脑渗透性NLRP3炎性小体抑制剂作为先导化合物和工具化合物。我们发现了一种小分子NLRP3炎性小体抑制剂NT-0527(11),并对其进行了广泛的分析,以揭示一种高效、选择性和脑渗透性的化合物。结果表明,该化合物具有口服生物利用度,在炎症模型中有效,且具有良好的可开发性特征。然而,NT-0527表现出CYP 2C19时间依赖性抑制作用,这使得其开发停滞,但该分子可作为一种有价值的工具化合物,用于研究涉及NLRP3炎性小体激活的神经炎症性疾病。