Evidence map›Paper›PMID 39950821›Full record

ArticleJournal of medicinal chemistry2025

Discovery of Novel Isoxazole-Based Small-Molecule Toll-Like Receptor 8 Antagonists.

Troy Matziol, Valerij Talagayev, Tjaša Slokan, Nika Strašek Benedik, Janine Holze, Matej Sova, Gerhard Wolber, Günther Weindl

Abstract read
In one paragraph

Article in Journal of medicinal chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. A high throughput assay to identify modulators of Death Receptor 3 (DR3).SLAS discovery : advancing life sciences R & D · 2026
    Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Troy MatziolPharmaceutical Institute, Pharmacology and Toxicology Section, University of Bonn, Gerhard-Domagk-Street 3, 53121 Bonn, Germany.
Valerij TalagayevInstitute of Pharmacy, Pharmaceutical and Medicinal ChemistryFreie, Universität Berlin, Königin-Luise-Street 2 + 4, 14195 Berlin, Germany.
Tjaša SlokanFaculty of Pharmacy, the Department of Pharmaceutical Chemistry, University of Ljubljana, Aškerčeva 7, SI-1000 Ljubljana, Slovenia.
Nika Strašek BenedikFaculty of Pharmacy, the Department of Pharmaceutical Chemistry, University of Ljubljana, Aškerčeva 7, SI-1000 Ljubljana, Slovenia.
Janine HolzePharmaceutical Institute, Pharmacology and Toxicology Section, University of Bonn, Gerhard-Domagk-Street 3, 53121 Bonn, Germany.
Matej SovaFaculty of Pharmacy, the Department of Pharmaceutical Chemistry, University of Ljubljana, Aškerčeva 7, SI-1000 Ljubljana, Slovenia.ORCID 0000-0002-8977-3450
Gerhard WolberInstitute of Pharmacy, Pharmaceutical and Medicinal ChemistryFreie, Universität Berlin, Königin-Luise-Street 2 + 4, 14195 Berlin, Germany.ORCID 0000-0002-5344-0048
Günther WeindlPharmaceutical Institute, Pharmacology and Toxicology Section, University of Bonn, Gerhard-Domagk-Street 3, 53121 Bonn, Germany.ORCID 0000-0002-4493-7597

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Toll-like receptor 8 (TLR8) recognizes viral and bacterial RNA, initiating inflammatory responses that are crucial for innate immunity. Dysregulated TLR8 signaling contributes to autoimmune diseases, including systemic lupus erythematosus and rheumatoid arthritis, driving chronic inflammation and tissue damage. Therefore, targeting TLR8 has gained attention as a promising therapeutic strategy. We report a novel selective TLR8 antagonist scaffold identified through computational modeling and simulation. In silico-guided rational drug design and synthesis led to potent isoxazole-based compounds that were characterized by structure-activity relationships. The most active compounds inhibited TLR8-mediated signaling in cell lines and primary cells, reduced MyD88 recruitment, suppressed NF-κB- and IRF-dependent signaling, and decreased inflammatory responses. In silico and pharmacological analyses demonstrated competitive binding to the pocket of chemical ligands within the TLR8 dimerization interface. These highly selective and potent TLR8 antagonists possess favorable physicochemical properties, representing potential clinical candidates for TLR8-targeted therapy.

Indexed as

IsoxazolesToll-Like Receptor 8AnimalsDrug DesignDrug DiscoveryHEK293 CellsHumansMiceMolecular Docking SimulationNF-kappa BSignal TransductionSmall Molecule LibrariesStructure-Activity RelationshipIsoxazolesNF-kappa BSmall Molecule LibrariesTLR8 protein, humanToll-Like Receptor 8

Identifiers

PMID39950821
PMCPMC12613816

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.