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High-Throughput Screening Campaign Identified a Potential Small Molecule RXFP3/4 Agonist
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 processi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709172/ https://www.ncbi.nlm.nih.gov/pubmed/34946593 http://dx.doi.org/10.3390/molecules26247511 |
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author | Lin, Guangyao Feng, Yang Cai, Xiaoqing Zhou, Caihong Shao, Lijun Chen, Yan Chen, Linhai Liu, Qing Zhou, Qingtong Bathgate, Ross A.D. Yang, Dehua Wang, Ming-Wei |
author_facet | Lin, Guangyao Feng, Yang Cai, Xiaoqing Zhou, Caihong Shao, Lijun Chen, Yan Chen, Linhai Liu, Qing Zhou, Qingtong Bathgate, Ross A.D. Yang, Dehua Wang, Ming-Wei |
author_sort | Lin, Guangyao |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8709172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87091722021-12-25 High-Throughput Screening Campaign Identified a Potential Small Molecule RXFP3/4 Agonist Lin, Guangyao Feng, Yang Cai, Xiaoqing Zhou, Caihong Shao, Lijun Chen, Yan Chen, Linhai Liu, Qing Zhou, Qingtong Bathgate, Ross A.D. Yang, Dehua Wang, Ming-Wei Molecules Communication 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. MDPI 2021-12-11 /pmc/articles/PMC8709172/ /pubmed/34946593 http://dx.doi.org/10.3390/molecules26247511 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Lin, Guangyao Feng, Yang Cai, Xiaoqing Zhou, Caihong Shao, Lijun Chen, Yan Chen, Linhai Liu, Qing Zhou, Qingtong Bathgate, Ross A.D. Yang, Dehua Wang, Ming-Wei High-Throughput Screening Campaign Identified a Potential Small Molecule RXFP3/4 Agonist |
title | High-Throughput Screening Campaign Identified a Potential Small Molecule RXFP3/4 Agonist |
title_full | High-Throughput Screening Campaign Identified a Potential Small Molecule RXFP3/4 Agonist |
title_fullStr | High-Throughput Screening Campaign Identified a Potential Small Molecule RXFP3/4 Agonist |
title_full_unstemmed | High-Throughput Screening Campaign Identified a Potential Small Molecule RXFP3/4 Agonist |
title_short | High-Throughput Screening Campaign Identified a Potential Small Molecule RXFP3/4 Agonist |
title_sort | high-throughput screening campaign identified a potential small molecule rxfp3/4 agonist |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709172/ https://www.ncbi.nlm.nih.gov/pubmed/34946593 http://dx.doi.org/10.3390/molecules26247511 |
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