Development of a first-in-class homolog-selective, covalent NOX4 inhibitor

The NADPH oxidase (NOX) family in humans includes seven enzymes whose main function is to produce reactive oxygen species. Because of their role in oxidative damage, these enzymes are being explored as targets for new therapies against oxidative stress-related diseases. However, their conserved catalytic core poses selective inhibition challenging. Current inhibitors suffer from low potency, cytotoxicity, assay interference, and poor selectivity. VAS2870, a covalent NOX inhibitor targeting a cysteine in the dehydrogenase (DH) domain, does not present assay interference but still shows limited selectivity, solubility, and safety. This study aimed to develop improved VAS2870-based targeted covalent inhibitors (TCIs) by designing and screening a library of cysteine-targeting compounds against NOX1, NOX2, NOX4, and NOX5. A hit compound, compound 2, was optimized, yielding a potent, homolog-selective NOX4 inhibitor, compound 18. Its mechanism of action was validated, demonstrating covalent binding to a cysteine residue and showing that compound binding is hindered by the presence of FAD in the DH domain.

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Journal
Biomedicine & Pharmacotherapy
Published
2026-08-14
DOI
https://doi.org/10.1016/j.biopha.2026.119844
Primary Topic
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Development of a first-in-class homolog-selective, covalent NOX4 inhibitor

Mariana Castelôa, Marta Massari, Fábio G. Martins, Andrea Mattevi et al.
Biomedicine & Pharmacotherapy
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
article

Development of a first-in-class homolog-selective, covalent NOX4 inhibitor

Mariana Castelôa, Marta Massari, Fábio G. Martins, Andrea Mattevi, Sara Marchese, Daniel Chavarria, Matteo Ré, Fernanda Borges, Lorenzo Basile, Sofia Benfeito, Carla Lima, Joana Reis, Sérgio F. Sousa, Inês Lima
article en

Abstract

The NADPH oxidase (NOX) family in humans includes seven enzymes whose main function is to produce reactive oxygen species. Because of their role in oxidative damage, these enzymes are being explored as targets for new therapies against oxidative stress-related diseases. However, their conserved catalytic core poses selective inhibition challenging. Current inhibitors suffer from low potency, cytotoxicity, assay interference, and poor selectivity. VAS2870, a covalent NOX inhibitor targeting a cysteine in the dehydrogenase (DH) domain, does not present assay interference but still shows limited selectivity, solubility, and safety. This study aimed to develop improved VAS2870-based targeted covalent inhibitors (TCIs) by designing and screening a library of cysteine-targeting compounds against NOX1, NOX2, NOX4, and NOX5. A hit compound, compound 2, was optimized, yielding a potent, homolog-selective NOX4 inhibitor, compound 18. Its mechanism of action was validated, demonstrating covalent binding to a cysteine residue and showing that compound binding is hindered by the presence of FAD in the DH domain.

Biomedicine & PharmacotherapyVol. 203
Universidade do Porto (PT), University of Pavia (IT), Istituto Nazionale per le Malattie Infettive Lazzaro Spallanzani (IT), University of Coimbra (PT)
Associazione Italiana per la Ricerca sul Cancro, Regione Lombardia, HORIZON EUROPE Framework Programme, Fundação para a Ciência e a Tecnologia, HORIZON EUROPE Marie Sklodowska-Curie Actions
Openalex Percentile: Top 15%
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
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