Evidence map›Paper›PMID 42289375›Full record

ArticleChemMedChem2026

Development of a Brain-Penetrant Nurr1 Agonist Tool.

Jan Vietor, Tanja Stiller, Christian Gege, Wael Saeb, Úrsula López-García, Hella Kohlhof, Daniel Vitt, Daniel Merk

Abstract read
In one paragraph

Article in ChemMedChem, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Jan VietorDepartment of Pharmacy, Ludwig-Maximilians-Universität München, Munich, Germany.
Tanja StillerDepartment of Pharmacy, Ludwig-Maximilians-Universität München, Munich, Germany.
Christian GegeImmunic AG, Gräfelfing, Germany.
Wael SaebRebisLab R&D GmbH, Planegg-Martinsried, Germany.
Úrsula López-GarcíaDepartment of Pharmacy, Ludwig-Maximilians-Universität München, Munich, Germany.
Hella KohlhofImmunic AG, Gräfelfing, Germany.
Daniel VittImmunic AG, Gräfelfing, Germany.
Daniel MerkDepartment of Pharmacy, Ludwig-Maximilians-Universität München, Munich, Germany.ORCID 0000-0002-5359-8128

Funding

European Research Council 101040355
6 · The paper itself

Abstract

The ligand-sensing transcription factor nuclear receptor-related 1 (Nurr1), is thought to mediate neuroprotective activity and is implicated in various neurodegenerative diseases. Nurr1 ligands have been developed as tools to capture the receptor's potential in vitro and in vivo, but a dedicated brain-targeting agonist has been lacking. Here, we employed the scaffold of the dihydroorotate dehydrogenase (DHODH) inhibitor and strong Nurr1 activator vidofludimus to develop a descendant with a high brain-to-blood ratio. Scaffold-hopping from cyclopentene to thiophene, enhanced fluorination, and replacement of the carboxylic acid by an amide provided a highly potent, selective, and brain-penetrant Nurr1 agonist to study the effects of Nurr1 activation in the central nervous system (CNS).

Indexed as

BrainNuclear Receptor Subfamily 4, Group A, Member 2ThiophenesAnimalsCyclopentanesDose-Response Relationship, DrugHumansMolecular StructureStructure-Activity RelationshipCyclopentanesNR4A2 protein, humanNuclear Receptor Subfamily 4, Group A, Member 2Thiophenesblood‐brain‐barrierNR4Anuclear receptor‐related 1transcription factor

Identifiers

PMID42289375
PMCPMC13265399

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.