Discovery of Nanomolar DCAF1 Small Molecule Ligands

Alice Shi Ming Li(Ontario Institute for Cancer Research), Serah Kimani(University Health Network), Brian J. Wilson(Ontario Institute for Cancer Research), Mahmoud Noureldin(Ontario Institute for Cancer Research), Héctor González-Álvarez(Ontario Institute for Cancer Research), Ahmed Mamai(Ontario Institute for Cancer Research), Laurent Hoffer(Ontario Institute for Cancer Research), John P. Guilinger, Ying Zhang, Moritz von Rechenberg(Relay Therapeutics (United States)), Jeremy S. Disch(Relay Therapeutics (United States)), Christopher J. Mulhern(Relay Therapeutics (United States)), Belinda L. Slakman(Relay Therapeutics (United States)), John W. Cuozzo(Relay Therapeutics (United States)), Aiping Dong(University of Toronto), Gennady Poda(Ontario Institute for Cancer Research), Mohammed Mohammed(Ontario Institute for Cancer Research), Punit Saraon(Ontario Institute for Cancer Research), Manish Mittal(Piramal (India)), Pratik Modh(Piramal (India)), V. Rathod(Piramal (India)), Bhashant Patel(Piramal (India)), Suzanne Ackloo(University of Toronto), Vijayaratnam Santhakumar(University of Toronto), Magdalena M. Szewczyk(University of Toronto), Dalia Baršytė-Lovejoy(University of Toronto), C.H. Arrowsmith(University Health Network), Richard Marcellus(Ontario Institute for Cancer Research), Marie-Aude Guié, Anthony D. Keefe, Peter J. Brown(University of Toronto), Levon Halabelian(University of Toronto), Rima Al‐awar(Ontario Institute for Cancer Research), Masoud Vedadi(Ontario Institute for Cancer Research)
Journal of Medicinal Chemistry
March 22, 2023
Cited by 64Open Access
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Abstract

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.


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