Suppr超能文献

用于 HNF4α 配体发现和化学生物基因组学的化学起始物质。

Chemical Starting Matter for HNF4α Ligand Discovery and Chemogenomics.

机构信息

Institute of Pharmaceutical Chemistry, Goethe University Frankfurt, Max-von-Laue-Str. 9, 60438 Frankfurt, Germany.

Structural Genomics Consortium, BMLS, Goethe-University Frankfurt, Max-von-Laue-Str. 15, 60438 Frankfurt, Germany.

出版信息

Int J Mol Sci. 2020 Oct 24;21(21):7895. doi: 10.3390/ijms21217895.

Abstract

Hepatocyte nuclear factor 4α (HNF4α) is a ligand-sensing transcription factor and presents as a potential drug target in metabolic diseases and cancer. In humans, mutations in the HNF4α gene cause maturity-onset diabetes of the young (MODY), and the elevated activity of this protein has been associated with gastrointestinal cancers. Despite the high therapeutic potential, available ligands and structure-activity relationship knowledge for this nuclear receptor are scarce. Here, we disclose a chemically diverse collection of orthogonally validated fragment-like activators as well as inverse agonists, which modulate HNF4α activity in a low micromolar range. These compounds demonstrate the druggability of HNF4α and thus provide a starting point for medicinal chemistry as well as an early tool for chemogenomics.

摘要

肝细胞核因子 4α(HNF4α)是一种配体感应转录因子,作为代谢疾病和癌症的潜在药物靶点。在人类中,HNF4α 基因突变会导致青少年发病的成年型糖尿病(MODY),而这种蛋白质的活性升高与胃肠道癌症有关。尽管具有很高的治疗潜力,但这种核受体的可用配体和结构-活性关系知识却很少。在这里,我们公开了一组化学多样性的正交验证片段样激活剂和反向激动剂,它们以低微摩尔范围调节 HNF4α 的活性。这些化合物证明了 HNF4α 的成药性,因此为药物化学提供了一个起点,也为化学生物基因组学提供了一个早期工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/953b/7660650/2c79e731b854/ijms-21-07895-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验