作者
Alice Shi Ming Li,Serah Kimani,Ahmed Aman,Mahmoud Noureldin,Héctor González-Álvarez,Ahmed Mamai,Laurent Hoffer,John P Guilinger,Ying Zhang,Moritz von Rechenberg,Jeremy S. Disch,Christopher J. Mulhern,Belinda L. Slakman,John W. Cuozzo,Aiping Dong,Gennady Poda,Mohammed Mohammed,Punit Saraon,Manish Mittal,Pratik Modh,Vaibhavi Rathod,Bhashant Patel,Suzanne Ackloo,Vijayaratnam Santhakumar,Magdalena M. Szewczyk,Dalia Baršytė-Lovejoy,C.H. Arrowsmith,Richard Marcellus,Marie-Aude Guié,Anthony D. Keefe,Peter J. Brown,Levon Halabelian,Rima Al‐awar,Masoud Vedadi
摘要
DCAF1 is a substrate receptor of two distinct E3 ligases (CRL4DCAF1 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 KD of 11 μM. Structure-guided hit optimization led to the discovery of OICR-8268 (26e) with an SPR KD of 38 nM and cellular target engagement with EC50 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.