Willems Henriëtte M G, Edwards Simon, Boffey Helen K, Chawner Stephen J, Green Christopher, Romero Tamara, Winpenny David, Skidmore John, Clarke Jonathan H, Andrews Stephen P
The ALBORADA Drug Discovery Institute, University of Cambridge Island Research Building, Cambridge Biomedical Campus, Hills Road Cambridge CB2 0AH UK
RSC Med Chem. 2023 Apr 17;14(5):934-946. doi: 10.1039/d3md00039g. eCollection 2023 May 25.
The phosphatidylinositol 5-phosphate 4-kinases (PI5P4Ks) play a central role in regulating cell signalling pathways and, as such, have become therapeutic targets for diseases such as cancer, neurodegeneration and immunological disorders. Many of the PI5P4Kα inhibitors that have been reported to date have suffered from poor selectivity and/or potency and the availability of better tool molecules would facilitate biological exploration. Herein we report a novel PI5P4Kα inhibitor chemotype that was identified through virtual screening. The series was optimised to deliver ARUK2002821 (36), a potent PI5P4Kα inhibitor (pIC = 8.0) which is selective other PI5P4K isoforms and has broad selectivity against lipid and protein kinases. ADMET and target engagement data are provided for this tool molecule and others in the series, as well as an X-ray structure of 36 solved in complex with its PI5P4Kα target.
磷脂酰肌醇5-磷酸4-激酶(PI5P4Ks)在调节细胞信号通路中起核心作用,因此已成为癌症、神经退行性疾病和免疫紊乱等疾病的治疗靶点。迄今为止报道的许多PI5P4Kα抑制剂都存在选择性差和/或效力低的问题,而更好的工具分子的可用性将有助于生物学探索。在此,我们报告了一种通过虚拟筛选鉴定出的新型PI5P4Kα抑制剂化学类型。该系列经过优化,得到了ARUK2002821(36),一种有效的PI5P4Kα抑制剂(pIC = 8.0),它对其他PI5P4K亚型具有选择性,并且对脂质和蛋白激酶具有广泛的选择性。本文提供了该工具分子及该系列其他分子的ADMET和靶点结合数据,以及36与其PI5P4Kα靶点复合物的X射线晶体结构。