Structural Genomics Consortium, University of Toronto, Toronto, Ontario M5G 1L7, Canada.
Drug Discovery Program, Ontario Institute for Cancer Research, Toronto, Ontario M5G 0A3, Canada.
J Med Chem. 2023 Apr 13;66(7):5041-5060. doi: 10.1021/acs.jmedchem.2c02132. Epub 2023 Mar 22.
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.
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。