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author Li, Alice Shi Ming
Kimani, Serah
Wilson, Brian
Noureldin, Mahmoud
González-Álvarez, Héctor
Mamai, Ahmed
Hoffer, Laurent
Guilinger, John P.
Zhang, Ying
von Rechenberg, Moritz
Disch, Jeremy S.
Mulhern, Christopher J.
Slakman, Belinda L.
Cuozzo, John W.
Dong, Aiping
Poda, Gennady
Mohammed, Mohammed
Saraon, Punit
Mittal, Manish
Modh, Pratik
Rathod, Vaibhavi
Patel, Bhashant
Ackloo, Suzanne
Santhakumar, Vijayaratnam
Szewczyk, Magdalena M
Barsyte-Lovejoy, Dalia
Arrowsmith, Cheryl H.
Marcellus, Richard
Guié, Marie-Aude
Keefe, Anthony D.
Brown, Peter J.
Halabelian, Levon
Al-awar, Rima
Vedadi, Masoud
author_facet Li, Alice Shi Ming
Kimani, Serah
Wilson, Brian
Noureldin, Mahmoud
González-Álvarez, Héctor
Mamai, Ahmed
Hoffer, Laurent
Guilinger, John P.
Zhang, Ying
von Rechenberg, Moritz
Disch, Jeremy S.
Mulhern, Christopher J.
Slakman, Belinda L.
Cuozzo, John W.
Dong, Aiping
Poda, Gennady
Mohammed, Mohammed
Saraon, Punit
Mittal, Manish
Modh, Pratik
Rathod, Vaibhavi
Patel, Bhashant
Ackloo, Suzanne
Santhakumar, Vijayaratnam
Szewczyk, Magdalena M
Barsyte-Lovejoy, Dalia
Arrowsmith, Cheryl H.
Marcellus, Richard
Guié, Marie-Aude
Keefe, Anthony D.
Brown, Peter J.
Halabelian, Levon
Al-awar, Rima
Vedadi, Masoud
author_sort Li, Alice Shi Ming
collection PubMed
description [Image: see text] 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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spelling pubmed-101083592023-04-18 Discovery of Nanomolar DCAF1 Small Molecule Ligands Li, Alice Shi Ming Kimani, Serah Wilson, Brian Noureldin, Mahmoud González-Álvarez, Héctor Mamai, Ahmed Hoffer, Laurent Guilinger, John P. Zhang, Ying von Rechenberg, Moritz Disch, Jeremy S. Mulhern, Christopher J. Slakman, Belinda L. Cuozzo, John W. Dong, Aiping Poda, Gennady Mohammed, Mohammed Saraon, Punit Mittal, Manish Modh, Pratik Rathod, Vaibhavi Patel, Bhashant Ackloo, Suzanne Santhakumar, Vijayaratnam Szewczyk, Magdalena M Barsyte-Lovejoy, Dalia Arrowsmith, Cheryl H. Marcellus, Richard Guié, Marie-Aude Keefe, Anthony D. Brown, Peter J. Halabelian, Levon Al-awar, Rima Vedadi, Masoud J Med Chem [Image: see text] 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. American Chemical Society 2023-03-22 /pmc/articles/PMC10108359/ /pubmed/36948210 http://dx.doi.org/10.1021/acs.jmedchem.2c02132 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Li, Alice Shi Ming
Kimani, Serah
Wilson, Brian
Noureldin, Mahmoud
González-Álvarez, Héctor
Mamai, Ahmed
Hoffer, Laurent
Guilinger, John P.
Zhang, Ying
von Rechenberg, Moritz
Disch, Jeremy S.
Mulhern, Christopher J.
Slakman, Belinda L.
Cuozzo, John W.
Dong, Aiping
Poda, Gennady
Mohammed, Mohammed
Saraon, Punit
Mittal, Manish
Modh, Pratik
Rathod, Vaibhavi
Patel, Bhashant
Ackloo, Suzanne
Santhakumar, Vijayaratnam
Szewczyk, Magdalena M
Barsyte-Lovejoy, Dalia
Arrowsmith, Cheryl H.
Marcellus, Richard
Guié, Marie-Aude
Keefe, Anthony D.
Brown, Peter J.
Halabelian, Levon
Al-awar, Rima
Vedadi, Masoud
Discovery of Nanomolar DCAF1 Small Molecule Ligands
title Discovery of Nanomolar DCAF1 Small Molecule Ligands
title_full Discovery of Nanomolar DCAF1 Small Molecule Ligands
title_fullStr Discovery of Nanomolar DCAF1 Small Molecule Ligands
title_full_unstemmed Discovery of Nanomolar DCAF1 Small Molecule Ligands
title_short Discovery of Nanomolar DCAF1 Small Molecule Ligands
title_sort discovery of nanomolar dcaf1 small molecule ligands
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108359/
https://www.ncbi.nlm.nih.gov/pubmed/36948210
http://dx.doi.org/10.1021/acs.jmedchem.2c02132
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