兴奋剂
G蛋白偶联受体
能量稳态
受体
化学
环磷酸腺苷
高通量筛选
内生
腺苷
配体(生物化学)
生物
内分泌学
生物化学
作者
Guangyao Lin,Yang Feng,Xiaoqing Cai,Caihong Zhou,Lijun Shao,Yan Chen,Linhai Chen,Qing Liu,Qingtong Zhou,Ross A. D. Bathgate,Dehua Yang,Ming‐Wei Wang
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2021-12-11
卷期号:26 (24): 7511-7511
被引量:8
标识
DOI:10.3390/molecules26247511
摘要
Relaxin/insulin-like family peptide receptor 3 (RXFP3) belongs to class A G protein-coupled receptor family. RXFP3 and its endogenous ligand relaxin-3 are mainly expressed in the brain with important roles in the regulation of appetite, energy metabolism, endocrine homeostasis and emotional processing. It is therefore implicated as a potential target for treatment of various central nervous system diseases. Since selective agonists of RXFP3 are restricted to relaxin-3 and its analogs, we conducted a high-throughput screening campaign against 32,021 synthetic and natural product-derived compounds using a cyclic adenosine monophosphate (cAMP) measurement-based method. Only one compound, WNN0109-C011, was identified following primary screening, secondary screening and dose-response studies. Although displayed agonistic effect in cells overexpressing the human RXFP3, it also showed cross-reactivity with the human RXFP4. This hit compound may provide not only a chemical probe to investigate the function of RXFP3/4, but also a novel scaffold for the development of RXFP3/4 agonists.
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