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Discovery of Nanomolar DCAF1 Small Molecule Ligands.

Alice Shi Ming LiSerah KimaniBrian WilsonMahmoud NoureldinHéctor González-ÁlvarezAhmed MamaiLaurent HofferJohn P GuilingerYing ZhangMoritz von RechenbergJeremy S DischChristopher J MulhernBelinda L SlakmanJohn W CuozzoAiping DongGennady PodaMohammed MohammedPunit SaraonManish MittalPratik ModhVaibhavi RathodBhashant PatelSuzanne AcklooVijayaratnam SanthakumarMagdalena M SzewczykDalia Barsyte-LovejoyCheryl H ArrowsmithRichard MarcellusMarie-Aude GuiéAnthony D KeefePeter J BrownLevon HalabelianRima Al-AwarMasoud Vedadi
Published in: Journal of medicinal chemistry (2023)
DCAF1 is a substrate receptor of two distinct E3 ligases (CRL4 DCAF1 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 K D of 11 μM. Structure-guided hit optimization led to the discovery of OICR-8268 ( 26e ) with an SPR K D of 38 nM and cellular target engagement with EC 50 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.
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