NR4A核受体化学工具的比较谱分析及化学基因组学应用

IF 6.8 1区 医学 Q1 CHEMISTRY, MEDICINAL
Sabine Willems,Vasily Morozov,Julian A Marschner,Daniel Merk
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引用次数: 0

摘要

NR4A家族的配体激活转录因子是具有神经保护和抗癌潜力的有前途的药物靶点,在药物发现中引起了强烈的关注。已经描述了几种NR4A调节剂,但缺乏一组经过验证的直接配体用于生物学研究。在这里,我们在几个正交试验系统中,在统一的条件下分析了报道的和市售的激动剂和逆激动剂,以建立一个高度注释的工具,并全面了解NR4A调节剂的特性。这一对比分析揭示了几种假定的NR4A配体缺乏靶向结合和调节,并验证了一组化学上不同的化合物作为基于化学基因组学的靶标鉴定研究的直接NR4A调节剂。未来的应用揭示了NR4A受体在内质网应激和脂肪细胞分化中的作用,证明了该组将孤儿靶点与表型效应联系起来的适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative Profiling and Chemogenomics Application of Chemical Tools for NR4A Nuclear Receptors.
The ligand-activated transcription factors of the NR4A family are implicated as promising drug targets with neuroprotective and anticancer potential and attract strong attention in drug discovery. Several NR4A modulators have been described, but a validated set of direct ligands for biological studies is lacking. Here, we profiled the reported and commercially available agonists and inverse agonists under uniform conditions in several orthogonal test systems to establish a highly annotated tool and gain comprehensive insights into the NR4A modulator characteristics. This comparative profiling revealed a lack of on-target binding and modulation for several putative NR4A ligands and validated a set of chemically diverse compounds as direct NR4A modulators for chemogenomics-based target identification studies. Prospective applications unveiled roles of NR4A receptors in endoplasmic reticulum stress and adipocyte differentiation, demonstrating suitability of the set to link the orphan targets with phenotypic effects.
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来源期刊
Journal of Medicinal Chemistry
Journal of Medicinal Chemistry 医学-医药化学
CiteScore
4.00
自引率
11.00%
发文量
804
审稿时长
1.9 months
期刊介绍: The Journal of Medicinal Chemistry is a prestigious biweekly peer-reviewed publication that focuses on the multifaceted field of medicinal chemistry. Since its inception in 1959 as the Journal of Medicinal and Pharmaceutical Chemistry, it has evolved to become a cornerstone in the dissemination of research findings related to the design, synthesis, and development of therapeutic agents. The Journal of Medicinal Chemistry is recognized for its significant impact in the scientific community, as evidenced by its 2022 impact factor of 7.3. This metric reflects the journal's influence and the importance of its content in shaping the future of drug discovery and development. The journal serves as a vital resource for chemists, pharmacologists, and other researchers interested in the molecular mechanisms of drug action and the optimization of therapeutic compounds.
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