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发现纳摩尔 DCAF1 小分子配体。

Discovery of Nanomolar DCAF1 Small Molecule Ligands.

机构信息

Structural Genomics Consortium, University of Toronto, Toronto, Ontario M5G 1L7, Canada.

Drug Discovery Program, Ontario Institute for Cancer Research, Toronto, Ontario M5G 0A3, Canada.

出版信息

J Med Chem. 2023 Apr 13;66(7):5041-5060. doi: 10.1021/acs.jmedchem.2c02132. Epub 2023 Mar 22.

Abstract

DCAF1 is a substrate receptor of two distinct E3 ligases (CRL4 and EDVP), plays a critical physiological role in protein degradation, and is considered a drug target for various cancers. Antagonists of DCAF1 could be used toward the development of therapeutics for cancers and viral treatments. We used the WDR domain of DCAF1 to screen a 114-billion-compound DNA encoded library (DEL) and identified candidate compounds using similarity search and machine learning. This led to the discovery of a compound (Z1391232269) with an SPR of 11 μM. Structure-guided hit optimization led to the discovery of OICR-8268 () with an SPR of 38 nM and cellular target engagement with EC of 10 μM as measured by cellular thermal shift assay (CETSA). OICR-8268 is an excellent tool compound to enable the development of next-generation DCAF1 ligands toward cancer therapeutics, further investigation of DCAF1 functions in cells, and the development of DCAF1-based PROTACs.

摘要

DCAF1 是两种不同的 E3 连接酶(CRL4 和 EDVP)的底物受体,在蛋白质降解中发挥着关键的生理作用,被认为是各种癌症的药物靶点。DCAF1 的拮抗剂可用于开发癌症和病毒治疗的治疗药物。我们使用 DCAF1 的 WDR 结构域筛选了一个 1140 亿个化合物的 DNA 编码文库(DEL),并使用相似性搜索和机器学习来鉴定候选化合物。这导致发现了一种化合物(Z1391232269),其 SPR 为 11 μM。基于结构的命中优化导致发现了 OICR-8268(),其 SPR 为 38 nM,并且通过细胞热转移测定(CETSA)测量的细胞靶标结合 EC 为 10 μM。OICR-8268 是一种极好的工具化合物,可用于开发下一代 DCAF1 配体以用于癌症治疗药物,进一步研究 DCAF1 在细胞中的功能,以及开发基于 DCAF1 的 PROTAC。

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