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虚拟筛选直接鉴定出新型具有纳摩尔活性的羧基酯酶 Notum 片段大小抑制剂。

Virtual Screening Directly Identifies New Fragment-Sized Inhibitors of Carboxylesterase Notum with Nanomolar Activity.

机构信息

Alzheimer's Research UK UCL Drug Discovery Institute, University College London, The Cruciform Building, Gower Street, LondonWC1E 6BT, U.K.

Division of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, The Henry Wellcome Building for Genomic Medicine, Roosevelt Drive, OxfordOX3 7BN, U.K.

出版信息

J Med Chem. 2022 Jan 13;65(1):562-578. doi: 10.1021/acs.jmedchem.1c01735. Epub 2021 Dec 23.

Abstract

Notum is a negative regulator of Wnt signaling acting through the hydrolysis of a palmitoleoylate ester, which is required for Wnt activity. Inhibitors of Notum could be of use in diseases where dysfunctional Notum activity is an underlying cause. A docking-based virtual screen (VS) of a large commercial library was used to shortlist 952 compounds for experimental validation as inhibitors of Notum. The VS was successful with 31 compounds having an IC < 500 nM. A critical selection process was then applied with two clusters and two singletons (-) selected for hit validation. Optimization of guided by structural biology identified potent inhibitors of Notum activity that restored Wnt/β-catenin signaling in cell-based models. The [1,2,4]triazolo[4,3-]pyradizin-3(2)-one series represent a new chemical class of Notum inhibitors and the first to be discovered by a VS campaign. These results demonstrate the value of VS with well-designed docking models based on X-ray structures.

摘要

Notum 是 Wnt 信号的负调节剂,通过水解棕榈油酸酯起作用,该酯对于 Wnt 活性是必需的。Notum 的抑制剂可能对功能失调的 Notum 活性是潜在病因的疾病有用。使用基于对接的虚拟筛选 (VS) 对大型商业文库进行筛选,以将 952 种化合物列为 Notum 抑制剂的实验验证。VS 成功地筛选出 31 种 IC < 500 nM 的化合物。然后应用了一个关键的选择过程,选择了两个簇和两个单一组分 (-) 进行命中验证。由结构生物学指导的优化确定了 Notum 活性的有效抑制剂,这些抑制剂在基于细胞的模型中恢复了 Wnt/β-catenin 信号传导。[1,2,4]三唑并[4,3-]哒嗪-3(2)-酮系列代表了一类新的 Notum 抑制剂,是通过 VS 活动首次发现的。这些结果证明了基于 X 射线结构的精心设计的对接模型的 VS 的价值。

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