Activity Analysis of the P2X Receptor Antagonist PPADS against Signal Transducer and Activator of Transcription Proteins

The small molecule PPADS is a P2X receptor antagonist. Analysis of a library of known bioactive compounds in competitive fluorescence polarization-based assays indicates that PPADS and its isomer iso-PPADS also possess activity against members of the signal transducer and activator of transcription (STAT) family of transcription factors, in particular STAT4, STAT5a, and STAT5b. These results are also supported by HTRF assays. PPADS protects STAT4 and STAT5a/STAT5b from thermal degradation in cell lysates to a higher extent than STAT3. Combined data from this article and a previous article suggest that aromatic disulfonate antagonists of P2X receptors might serve as promising starting points for the development of inhibitors of STAT proteins.

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Publication Details

Journal
ChemBioChem
Published
2025-07-24
DOI
https://doi.org/10.1002/cbic.202500454
Citations
1
Primary Topic
Cytokine Signaling Pathways and Interactions
Type
article
Field-Weighted Citation Impact
1.05

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article

Activity Analysis of the P2X Receptor Antagonist PPADS against Signal Transducer and Activator of Transcription Proteins

Thorsten Berg, Angela Berg, Martin Gräber
1 citations
ChemBioChem
Cytokine Signaling Pathways and Interactions
1.05
article

Activity Analysis of the P2X Receptor Antagonist PPADS against Signal Transducer and Activator of Transcription Proteins

Thorsten Berg, Angela Berg, Martin Gräber
article en
1 citations

Abstract

The small molecule PPADS is a P2X receptor antagonist. Analysis of a library of known bioactive compounds in competitive fluorescence polarization-based assays indicates that PPADS and its isomer iso-PPADS also possess activity against members of the signal transducer and activator of transcription (STAT) family of transcription factors, in particular STAT4, STAT5a, and STAT5b. These results are also supported by HTRF assays. PPADS protects STAT4 and STAT5a/STAT5b from thermal degradation in cell lysates to a higher extent than STAT3. Combined data from this article and a previous article suggest that aromatic disulfonate antagonists of P2X receptors might serve as promising starting points for the development of inhibitors of STAT proteins.

ChemBioChemVol. 26(17)
Center for Integrated Protein Science Munich (DE), Max Planck Institute of Biochemistry (DE), Leipzig University (DE)
Deutsche Forschungsgemeinschaft
Openalex Percentile: Top 19%
Cytokine Signaling Pathways and Interactions
1.05
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