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Structure, Function, and Pharmaceutical Ligands of 5-Hydroxytryptamine 2B Receptor

Since the first characterization of the 5-hydroxytryptamine 2B receptor (5-HT(2B)R) in 1992, significant progress has been made in 5-HT(2B)R research. Herein, we summarize the biological function, structure, and small-molecule pharmaceutical ligands of the 5-HT(2B)R. Emerging evidence has suggested...

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Autores principales: Wang, Qing, Zhou, Yu, Huang, Jianhui, Huang, Niu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7909583/
https://www.ncbi.nlm.nih.gov/pubmed/33498477
http://dx.doi.org/10.3390/ph14020076
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author Wang, Qing
Zhou, Yu
Huang, Jianhui
Huang, Niu
author_facet Wang, Qing
Zhou, Yu
Huang, Jianhui
Huang, Niu
author_sort Wang, Qing
collection PubMed
description Since the first characterization of the 5-hydroxytryptamine 2B receptor (5-HT(2B)R) in 1992, significant progress has been made in 5-HT(2B)R research. Herein, we summarize the biological function, structure, and small-molecule pharmaceutical ligands of the 5-HT(2B)R. Emerging evidence has suggested that the 5-HT(2B)R is implicated in the regulation of the cardiovascular system, fibrosis disorders, cancer, the gastrointestinal (GI) tract, and the nervous system. Eight crystal complex structures of the 5-HT(2B)R bound with different ligands provided great insights into ligand recognition, activation mechanism, and biased signaling. Numerous 5-HT(2B)R antagonists have been discovered and developed, and several of them have advanced to clinical trials. It is expected that the novel 5-HT(2B)R antagonists with high potency and selectivity will lead to the development of first-in-class drugs in various therapeutic areas.
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spelling pubmed-79095832021-02-27 Structure, Function, and Pharmaceutical Ligands of 5-Hydroxytryptamine 2B Receptor Wang, Qing Zhou, Yu Huang, Jianhui Huang, Niu Pharmaceuticals (Basel) Review Since the first characterization of the 5-hydroxytryptamine 2B receptor (5-HT(2B)R) in 1992, significant progress has been made in 5-HT(2B)R research. Herein, we summarize the biological function, structure, and small-molecule pharmaceutical ligands of the 5-HT(2B)R. Emerging evidence has suggested that the 5-HT(2B)R is implicated in the regulation of the cardiovascular system, fibrosis disorders, cancer, the gastrointestinal (GI) tract, and the nervous system. Eight crystal complex structures of the 5-HT(2B)R bound with different ligands provided great insights into ligand recognition, activation mechanism, and biased signaling. Numerous 5-HT(2B)R antagonists have been discovered and developed, and several of them have advanced to clinical trials. It is expected that the novel 5-HT(2B)R antagonists with high potency and selectivity will lead to the development of first-in-class drugs in various therapeutic areas. MDPI 2021-01-20 /pmc/articles/PMC7909583/ /pubmed/33498477 http://dx.doi.org/10.3390/ph14020076 Text en © 2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Wang, Qing
Zhou, Yu
Huang, Jianhui
Huang, Niu
Structure, Function, and Pharmaceutical Ligands of 5-Hydroxytryptamine 2B Receptor
title Structure, Function, and Pharmaceutical Ligands of 5-Hydroxytryptamine 2B Receptor
title_full Structure, Function, and Pharmaceutical Ligands of 5-Hydroxytryptamine 2B Receptor
title_fullStr Structure, Function, and Pharmaceutical Ligands of 5-Hydroxytryptamine 2B Receptor
title_full_unstemmed Structure, Function, and Pharmaceutical Ligands of 5-Hydroxytryptamine 2B Receptor
title_short Structure, Function, and Pharmaceutical Ligands of 5-Hydroxytryptamine 2B Receptor
title_sort structure, function, and pharmaceutical ligands of 5-hydroxytryptamine 2b receptor
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7909583/
https://www.ncbi.nlm.nih.gov/pubmed/33498477
http://dx.doi.org/10.3390/ph14020076
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