Discovery of UCB9386: A Potent, Selective, and Brain-Penetrant Nuak1 Inhibitor Suitable for <i>In Vivo</i> Pharmacological Studies

Nuak1 (NUAK family SnF1-like kinase-1) is a serine-threonine kinase and a member of the AMPK family. Interest in Nuak1 has increased over the years due to the role it plays in several biological processes, from tumor cell invasion and proliferation to Tau stabilization. Nuak1 is expressed in many cancer cell lines and many reports describe this target as an oncogene, the inhibition of which is hypothesized to be valuable for treating various cancer types including glioma. We report here the discovery of Nuak1 inhibitors originating from HTS hit <b>9</b> with excellent selectivity and the subsequent medicinal chemistry optimization program, supported by structural information from the first crystal structures of a Nuak1 chimeric protein which provided insights into the binding modes of our compounds. These efforts yielded a nanomolar cell potent, highly selective and brain penetrant Nuak1 inhibitor UCB9386 (<b>56</b>) suitable for <i>in vivo</i> pharmacological studies for central nervous system (CNS) disorders.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2024-11-26
DOI
https://doi.org/10.1021/acs.jmedchem.4c01237
Citations
4
Primary Topic
Genetics and Neurodevelopmental Disorders
Type
article
Field-Weighted Citation Impact
2.20

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article

Discovery of UCB9386: A Potent, Selective, and Brain-Penetrant Nuak1 Inhibitor Suitable for In Vivo Pharmacological Studies

Teresa de Haro, S.L. Delker, Claude Delatour, Eric Jnoff et al.
4 citations
Journal of Medicinal Chemistry
Genetics and Neurodevelopmental Disorders
2.20
article

Discovery of UCB9386: A Potent, Selective, and Brain-Penetrant Nuak1 Inhibitor Suitable for In Vivo Pharmacological Studies

Teresa de Haro, S.L. Delker, Claude Delatour, Eric Jnoff, Veerle De Wever, Atul R. Gholap, Nathalie Van Hijfte, Adrian Hall, Jan Abendroth, Simon Verheijden, Thierry Demaude, Mark Calmiano, Karine G. Poullennec, Nilesh Gaikwad, Jean‐Philippe Courade, Á. de Pablo Cárdenas, Dnyaneshwar Ghavate, Magdalena Kierkowicz, Régis Le Mestre, Katerina Vernerova, Nivrutti Waghmode, Naresh Bhuma, Laurent Calmus
article en
4 citations

Abstract

Nuak1 (NUAK family SnF1-like kinase-1) is a serine-threonine kinase and a member of the AMPK family. Interest in Nuak1 has increased over the years due to the role it plays in several biological processes, from tumor cell invasion and proliferation to Tau stabilization. Nuak1 is expressed in many cancer cell lines and many reports describe this target as an oncogene, the inhibition of which is hypothesized to be valuable for treating various cancer types including glioma. We report here the discovery of Nuak1 inhibitors originating from HTS hit <b>9</b> with excellent selectivity and the subsequent medicinal chemistry optimization program, supported by structural information from the first crystal structures of a Nuak1 chimeric protein which provided insights into the binding modes of our compounds. These efforts yielded a nanomolar cell potent, highly selective and brain penetrant Nuak1 inhibitor UCB9386 (<b>56</b>) suitable for <i>in vivo</i> pharmacological studies for central nervous system (CNS) disorders.

Journal of Medicinal ChemistryVol. 67(23)
Janssen (Belgium) (BE), Urban College of Boston (US), University College Birmingham (GB), Bone Therapeutics (BE), Illumina (United Kingdom) (GB), BenevolentAI (United Kingdom) (GB), UCB Pharma (Belgium) (BE)
UCB
Zero hunger
Openalex Percentile: Top 11%
Genetics and Neurodevelopmental Disorders
2.20
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