日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Structural Tuning of Vidofludimus for High-Efficacy NR4A Agonism.

Vidofludimus 的结构调控以实现高效 NR4A 激动作用。

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

Dual Nurr1/RXR agonism of valerenic acid and synthetic mimetics enables dimer-selective Nurr1 modulation

缬草酸及其合成类似物对 Nurr1/RXR 的双重激动作用可实现对二聚体选择性的 Nurr1 调控。

Scholz, Katharina; López-García, Úrsula; Busch, Romy; Marschner, Julian A; Merk, Daniel

Carboxylic Acid Bioisosteres Boost Nurr1 Agonist Selectivity

羧酸生物等排体增强 Nurr1 激动剂选择性

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

A Nurr1 Agonist Derived from the Natural Ligand DHI Induces Neuroprotective Gene Expression.

源自天然配体DHI的Nurr1激动剂可诱导神经保护基因表达

Egner Markus, Busch Romy, López-García Úrsula, Lewandowski Max, Höfner Georg, Wein Thomas, Marschner Julian A, Merk Daniel

Fragment-Based Discovery of Drug-like LRH-1 Agonists

基于片段的类药LRH-1激动剂发现

Lang, Alisa; Ildefeld, Niklas; Lillich, Felix F; Kaiser, Astrid; Busch, Romy; Marschner, Julian A; Proschak, Ewgenij; Heering, Jan; Schubert-Zsilavecz, Manfred; Merk, Daniel

Comparative Evaluation and Profiling of Chemical Tools for the Nuclear Hormone Receptor Family 2.

核激素受体家族 2 化学工具的比较评价和分析

Lewandowski Max, Busch Romy, Marschner Julian A, Merk Daniel