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Discovery of Substituted 5-(2-Hydroxybenzoyl)-2-Pyridone Analogues as Inhibitors of the Human Caf1/CNOT7 Ribonuclease

Kaur, Ishwinder; Jadhav, Gopal P.; Fischer, Peter M.; Winkler, Gerlof Sebastiaan

Discovery of Substituted 5-(2-Hydroxybenzoyl)-2-Pyridone Analogues as Inhibitors of the Human Caf1/CNOT7 Ribonuclease Thumbnail


Authors

Ishwinder Kaur

Gopal P. Jadhav

Peter M. Fischer



Abstract

The Caf1/CNOT7 nuclease is a catalytic component of the Ccr4-Not deadenylase complex, which is a key regulator of post-transcriptional gene regulation. In addition to providing catalytic activity, Caf1/CNOT7 and its paralogue Caf1/CNOT8 also contribute a structural function by mediating interactions between the large, non-catalytic subunit CNOT1, which forms the backbone of the Ccr4-Not complex and the second nuclease subunit Ccr4 (CNOT6/CNOT6L). To facilitate investigations into the role of Caf1/CNOT7 in gene regulation, we aimed to discover and develop non-nucleoside inhibitors of the enzyme. Here, we disclose that the tri-substituted 2-pyridone compound 5-(5-bromo-2-hydroxy-benzoyl)-1-(4-chloro-2-methoxy-5-methyl-phenyl)-2-oxo-pyridine-3-carbonitrile is an inhibitor of the Caf1/CNOT7 nuclease. Using a fluorescence-based nuclease assay, the activity of 16 structural analogues was determined, which predominantly explored substituents on the 1-phenyl group. While no compound with higher potency was identified among this set of structural analogues, the lowest potency was observed with the analogue lacking substituents on the 1-phenyl group. This indicates that substituents on the 1-phenyl group contribute significantly to binding. To identify possible binding modes of the inhibitors, molecular docking was carried out. This analysis suggested that the binding modes of the five most potent inhibitors may display similar conformations upon binding active site residues. Possible interactions include π-π interactions with His225, hydrogen bonding with the backbone of Phe43 and Van der Waals interactions with His225, Leu209, Leu112 and Leu115.

Citation

Kaur, I., Jadhav, G. P., Fischer, P. M., & Winkler, G. S. (2024). Discovery of Substituted 5-(2-Hydroxybenzoyl)-2-Pyridone Analogues as Inhibitors of the Human Caf1/CNOT7 Ribonuclease. Molecules, 29(18), Article 4351. https://doi.org/10.3390/molecules29184351

Journal Article Type Article
Acceptance Date Sep 12, 2024
Online Publication Date Sep 13, 2024
Publication Date Sep 13, 2024
Deposit Date Sep 16, 2024
Publicly Available Date Sep 16, 2024
Journal Molecules
Electronic ISSN 1420-3049
Publisher MDPI
Peer Reviewed Peer Reviewed
Volume 29
Issue 18
Article Number 4351
DOI https://doi.org/10.3390/molecules29184351
Keywords Caf1; CNOT7; CNOT8; mRNA; deadenylase; inhibitor; nuclease; gene regulation
Public URL https://nottingham-repository.worktribe.com/output/39715776
Publisher URL https://www.mdpi.com/1420-3049/29/18/4351

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