Structural Tuning of Vidofludimus for High-Efficacy NR4A Agonism

The nerve growth factor IB-like receptors (NR4A) are (neuro)protective transcription factors as part of the immediate early response and hold potential in various pathologies, including neurodegeneration. Despite recent progress in NR4A ligand development, high-quality chemical tools to probe phenotypic effects of NR4A modulation are still rare, and a selective agonist with strong efficacy is lacking. Here, we developed a potent and selective NR4A activator equipped with distinctly high agonist efficacy building on the scaffold of the dihydroorotate dehydrogenase inhibitor and nuclear receptor-related 1 agonist vidofludimus. We identified structural modifications conveying potency, selectivity, and efficacy via systematic structure-activity relationship elucidation, and fusion of favored motifs eventually enabled multiparameter optimization to a chemical tool meeting highest quality criteria for biological studies.

Authors

Institutions

Publication Details

Journal
Journal of Medicinal Chemistry
Published
2026-01-26
DOI
https://doi.org/10.1021/acs.jmedchem.5c03217
Primary Topic
Nuclear Receptors and Signaling
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Structural Tuning of Vidofludimus for High-Efficacy NR4A Agonism

Daniel Merk, Romy Busch, Jan Vietor, Úrsula López-García et al.
Journal of Medicinal Chemistry
Nuclear Receptors and Signaling
article

Structural Tuning of Vidofludimus for High-Efficacy NR4A Agonism

Daniel Merk, Romy Busch, Jan Vietor, Úrsula López-García, Christian Gege, Tanja Stiller, Anna Maria Thommes
article en

Abstract

The nerve growth factor IB-like receptors (NR4A) are (neuro)protective transcription factors as part of the immediate early response and hold potential in various pathologies, including neurodegeneration. Despite recent progress in NR4A ligand development, high-quality chemical tools to probe phenotypic effects of NR4A modulation are still rare, and a selective agonist with strong efficacy is lacking. Here, we developed a potent and selective NR4A activator equipped with distinctly high agonist efficacy building on the scaffold of the dihydroorotate dehydrogenase inhibitor and nuclear receptor-related 1 agonist vidofludimus. We identified structural modifications conveying potency, selectivity, and efficacy via systematic structure-activity relationship elucidation, and fusion of favored motifs eventually enabled multiparameter optimization to a chemical tool meeting highest quality criteria for biological studies.

Journal of Medicinal ChemistryVol. 69(3)
Immune Regulation (United Kingdom) (GB), Ludwig-Maximilians-Universität München (DE)
European Commission, Fraunhofer-Institut für Zelltherapie und Immunologie
Openalex Percentile: Top 79%
Nuclear Receptors and Signaling
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.