Fragment-based discovery of orphan nuclear receptor Nur77/NGFI-B ligands

被引:2
|
作者
Arifi, Silvia [1 ]
Zaienne, Daniel [1 ]
Heering, Jan [2 ]
Wein, Thomas [3 ]
Zhubi, Rezart [1 ,4 ]
Chaikuad, Apirat [1 ,4 ]
Knapp, Stefan [1 ,4 ]
Marschner, Julian A. [3 ]
Merk, Daniel [1 ,3 ]
机构
[1] Goethe Univ Frankfurt, Inst Pharmaceut Chem, D-60438 Frankfurt, Germany
[2] Fraunhofer Inst Translat Med & Pharmacol ITMP, D-60596 Frankfurt, Germany
[3] Ludwig Maximilians Univ Munchen, Dept Pharm, D-81377 Munich, Germany
[4] Goethe Univ Frankfurt, BMLS, Struct Genom Consortium, D-60438 Frankfurt, Germany
关键词
Transcription factor; NR4A; Cancer; Neurodegeneration; Virtual screening; IN-VITRO; NUR77; NURR1; INFLAMMATION; AGONIST; NR4A1; BIND; ACID;
D O I
10.1016/j.bioorg.2022.106164
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The transcription factor nerve growth factor-induced clone B (NGFI-B, Nur77, NR4A1) is an orphan nuclear receptor playing a role in cell survival and apoptosis regulation. Pharmacological Nur77 modulation holds promise for cancer and (neuro-)inflammatory disease treatment. The available Nur77 ligand scaffolds based on highly lipophilic natural products cytosporone B, celastrol and isoalantolactone are inadequate for the development of potent Nur77 modulators with favorable properties as chemical tools and future drugs. By fragment library screening and subsequent modeling for fragment extension, we have obtained a set of new Nur77 ligands offering alternative chemotypes for the development of Nur77 agonists and inverse agonists. Computer-aided fragment extension in a second stage screening yielded a Nur77 agonist with significant activation efficacy and preference over the related NR4A receptors.
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页数:9
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