Biaryl Phosphate‐Based Inhibitors of the Transcription Factor STAT4

The transcription factor signal transducer and activator of transcription (STAT)4 is a potential target for autoimmune diseases, such as inflammatory bowel disease, multiple sclerosis, rheumatoid arthritis, and diabetes mellitus. p-Biphenyl phosphate is reported as an inhibitor of the STAT4 Src homology 2 domain, and it is developed to the phosphonate-based inhibitor Stafori-1. Herein, structure-activity relationships of p-biaryl phosphates against STAT4 and their selectivity profiles against other STAT proteins are reported. The most potent biaryl phosphate-based inhibitor originating from this article, Stafori-2, contains the same aryl moieties as the phosphonate Stafori-1. However, Stafori-2 is more potent than Stafori-1 in fluorescence polarization assays and by isothermal titration calorimetry.

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Publication Details

Journal
ChemMedChem
Published
2025-09-09
DOI
https://doi.org/10.1002/cmdc.202500672
Primary Topic
Cytokine Signaling Pathways and Interactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Biaryl Phosphate‐Based Inhibitors of the Transcription Factor STAT4

Thorsten Berg, Christoph Protzel, Nadiya Brovchenko, Anne Maria Oelsch
ChemMedChem
Cytokine Signaling Pathways and Interactions
article

Biaryl Phosphate‐Based Inhibitors of the Transcription Factor STAT4

Thorsten Berg, Christoph Protzel, Nadiya Brovchenko, Anne Maria Oelsch
article en

Abstract

The transcription factor signal transducer and activator of transcription (STAT)4 is a potential target for autoimmune diseases, such as inflammatory bowel disease, multiple sclerosis, rheumatoid arthritis, and diabetes mellitus. p-Biphenyl phosphate is reported as an inhibitor of the STAT4 Src homology 2 domain, and it is developed to the phosphonate-based inhibitor Stafori-1. Herein, structure-activity relationships of p-biaryl phosphates against STAT4 and their selectivity profiles against other STAT proteins are reported. The most potent biaryl phosphate-based inhibitor originating from this article, Stafori-2, contains the same aryl moieties as the phosphonate Stafori-1. However, Stafori-2 is more potent than Stafori-1 in fluorescence polarization assays and by isothermal titration calorimetry.

ChemMedChemVol. 20(21)
Leipzig University (DE)
Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, European Social Fund
Openalex Percentile: Top 67%
Cytokine Signaling Pathways and Interactions
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