The Discovery ofGSK3227634: A Potent Inhaled Inhibitorof the KEAP1/NRF2 Protein–Protein Interaction for the Treatmentof Chronic Obstructive Pulmonary Disease

Abstract KEAP1 is the key regulator of the NRF2-mediated cytoprotective response and a target for pathologies involving oxidative stress. Compounds that covalently modify KEAP1 to activate NRF2 are clinically validated; however, their chemical reactivity may drive increased off–target activity. A more selective approach involves inhibition of the KEAP1-NRF2 protein–protein interaction as exemplified by our previous bis-aryl lead KI-696 (4). We now describe the lead optimization of the bis-aryl series that focused on increasing the population of the bioactive conformation of the free ligand to drive potency while optimizing overall physicochemical properties. This resulted in the discovery of GSK3227634 (5), an ultrahigh-affinity noncovalent inhibitor of KEAP1-NRF2 (surface plasmon resonance pKd = 10.9) and the first NRF2 activator to demonstrate target engagement and efficacy in preclinical models of oxidative stress via direct delivery to the lung. Compound 5 therefore represents a novel potential agent to treat lung diseases involving oxidative stress, such as chronic obstructive pulmonary disease.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2026-08-14
DOI
https://doi.org/10.1021/acs.jmedchem.6c01820
Primary Topic
Genomics, phytochemicals, and oxidative stress
Type
article
Field-Weighted Citation Impact
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article

The Discovery ofGSK3227634: A Potent Inhaled Inhibitorof the KEAP1/NRF2 Protein–Protein Interaction for the Treatmentof Chronic Obstructive Pulmonary Disease

Paris Ward, Sabrina Bédard, Nicole C. Goodwin, Casey Kmett et al.
Journal of Medicinal Chemistry
Genomics, phytochemicals, and oxidative stress
article

The Discovery ofGSK3227634: A Potent Inhaled Inhibitorof the KEAP1/NRF2 Protein–Protein Interaction for the Treatmentof Chronic Obstructive Pulmonary Disease

Paris Ward, Sabrina Bédard, Nicole C. Goodwin, Casey Kmett, Tom D. Heightman, Tindy Li, Jeffrey K. Kerns, Thomas G. Davies, Dirk Eberhard, Thilo Werner, Royston C. B. Copley, Ruth R. Osborn, Torren M. Peakman, Steven R. Katchur, Marcus Bantscheff, Alison J.‐A. Woolford, Charles J. Kotzer, William L. Rumsey, Patricia L. Podolin, Lawrence A. Wolfe, Yolanda Sánchez, Roderick Davis, Marcel Mülbaier, Hongxing Yan, Zining Wu, Hong Nie, James F. Callahan, Philip Landis, Derrick Meinhold, Thomas Sweitzer, Catherine Booth-Genthe, Jeffrey Boehm, Nestor Concha, Pearl Flamberg, Joseph Foley, Alicia Davis, Brian Peck
article en

Abstract

Abstract KEAP1 is the key regulator of the NRF2-mediated cytoprotective response and a target for pathologies involving oxidative stress. Compounds that covalently modify KEAP1 to activate NRF2 are clinically validated; however, their chemical reactivity may drive increased off–target activity. A more selective approach involves inhibition of the KEAP1-NRF2 protein–protein interaction as exemplified by our previous bis-aryl lead KI-696 (4). We now describe the lead optimization of the bis-aryl series that focused on increasing the population of the bioactive conformation of the free ligand to drive potency while optimizing overall physicochemical properties. This resulted in the discovery of GSK3227634 (5), an ultrahigh-affinity noncovalent inhibitor of KEAP1-NRF2 (surface plasmon resonance pKd = 10.9) and the first NRF2 activator to demonstrate target engagement and efficacy in preclinical models of oxidative stress via direct delivery to the lung. Compound 5 therefore represents a novel potential agent to treat lung diseases involving oxidative stress, such as chronic obstructive pulmonary disease.

Journal of Medicinal Chemistry
University of Hertfordshire (GB), South College (US), Immunomedics (Germany) (DE), GW Pharmaceuticals (United Kingdom) (GB)
Good health and well-being
Openalex Percentile: Top 16%
Genomics, phytochemicals, and oxidative stress
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