Discovery of ATX968: An Orally Available Allosteric Inhibitor of DHX9

DHX9 is an RNA/DNA helicase integral in the maintenance of genome stability that has emerged as an attractive target for oncology drug discovery. Disclosed herein is the discovery and optimization of a series of DHX9 inhibitors. Compound <b>1</b> was identified as a partial inhibitor of DHX9 ATPase activity but a full inhibitor of unwinding activity. Binding of <b>1</b> to a pocket distinct from the ATP binding site was confirmed by X-ray crystallography, enabling structure-based drug optimization. During this optimization, a sulfur-halogen bond was identified that increased on-target residence time without impacting equilibrium binding affinity. Analysis shows that cell potency more closely correlates with residence time than with equilibrium measurements of binding affinity or biochemical potency. Further optimization of potency and ADME properties led to the identification of <b>ATX968</b>, a potent and selective DHX9 inhibitor that is efficacious in a tumor xenograft model of microsatellite instability-high (MSI-H) colorectal cancer.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2025-04-29
DOI
https://doi.org/10.1021/acs.jmedchem.5c00252
Citations
7
Primary Topic
Cytokine Signaling Pathways and Interactions
Type
article
Field-Weighted Citation Impact
7.32
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article

Discovery of ATX968: An Orally Available Allosteric Inhibitor of DHX9

Deepali Gotur, Simina Grigoriu, Jae Eun Cheong, E. Allen Sickmier et al.
7 citations
Journal of Medicinal Chemistry
Cytokine Signaling Pathways and Interactions
7.32
article

Discovery of ATX968: An Orally Available Allosteric Inhibitor of DHX9

Deepali Gotur, Simina Grigoriu, Jae Eun Cheong, E. Allen Sickmier, Brian A. Sparling, David Brennan, Kenneth W. Duncan, Julie Liu, Serena J. Silver, Shihua Yao, G.J. Lockbaum, P. Ann Boriack‐Sjodin, Scott Ribich, Young‐Tae Lee, Matthew H. Daniels, Robert A. Copeland, Steve J. Blakemore, Shane M. Buker, Kevin E. Knockenhauer, Jennifer Castro, Chuang Lu
article en
7 citations

Abstract

DHX9 is an RNA/DNA helicase integral in the maintenance of genome stability that has emerged as an attractive target for oncology drug discovery. Disclosed herein is the discovery and optimization of a series of DHX9 inhibitors. Compound <b>1</b> was identified as a partial inhibitor of DHX9 ATPase activity but a full inhibitor of unwinding activity. Binding of <b>1</b> to a pocket distinct from the ATP binding site was confirmed by X-ray crystallography, enabling structure-based drug optimization. During this optimization, a sulfur-halogen bond was identified that increased on-target residence time without impacting equilibrium binding affinity. Analysis shows that cell potency more closely correlates with residence time than with equilibrium measurements of binding affinity or biochemical potency. Further optimization of potency and ADME properties led to the identification of <b>ATX968</b>, a potent and selective DHX9 inhibitor that is efficacious in a tumor xenograft model of microsatellite instability-high (MSI-H) colorectal cancer.

Journal of Medicinal ChemistryVol. 68(9)
Accent Therapeutics (United States) (US)
Openalex Percentile: Top 3%
Cytokine Signaling Pathways and Interactions
7.32
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