Movatterモバイル変換


[0]ホーム

URL:


Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
Thehttps:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

NIH NLM Logo
Log inShow account info
Access keysNCBI HomepageMyNCBI HomepageMain ContentMain Navigation
pubmed logo
Advanced Clipboard
User Guide

Full text links

Wiley full text link Wiley
Full text links

Actions

Share

Review
.2021 Nov 5;16(21):3263-3270.
doi: 10.1002/cmdc.202100395. Epub 2021 Aug 21.

25CN-NBOH: A Selective Agonist for in vitro and in vivo Investigations of the Serotonin 2A Receptor

Affiliations
Review

25CN-NBOH: A Selective Agonist for in vitro and in vivo Investigations of the Serotonin 2A Receptor

Emil Märcher Rørsted et al. ChemMedChem..

Abstract

4-(2-((2-hydroxybenzyl)amino)ethyl)-2,5-dimethoxybenzonitrile (25CN-NBOH) was first reported as a potent and selective serotonin 2A receptor (5-HT2A R) agonist in 2014, and it has since found extensive use as a pharmacological tool in a variety of in vitro, ex vivo and in vivo studies. 25CN-NBOH is readily available from a synthetic perspective using standard chemical transformations, and displays favorable physiochemical properties in terms of stability and solubility. Due to its superior selectivity for 5-HT2A R, 25CN-NBOH has been used to investigate the effects of selective 5-HT2A R activation in vivo, and has thus become an important pharmacological tool for the exploration of 5-HT2A R signaling in a range of animal models. In the present review, we outline the discovery of 25CN-NBOH, its pharmacological profile and major findings from studies where it has been used.

Keywords: 5-HT2A; Serotonin; agonist; psychedelics; selectivity.

© 2021 Wiley-VCH GmbH.

PubMed Disclaimer

Similar articles

See all similar articles

Cited by

See all "Cited by" articles

References

    1. T. A. Mestre, M. Zurowski, S. H. Fox, Expert Opin. Invest. Drugs 2013, 22, 411-421.
    1. F. X. Vollenweider, K. H. Preller, Nat. Rev. Neurosci. 2020, 21, DOI 10.1038/s41583-020-0367-2.
    1. A. A. Jensen, J. D. McCorvy, S. L. Petersen, C. Bundgaard, G. Liebscher, T. P. Kenakin, H. Brauner-Osborne, J. Kehler, J. L. Kristensen, J. Pharmacol. Exp. Ther. 2017, 361, 441-453.
    1. R. R. Griffiths, M. W. Johnson, M. A. Carducci, A. Umbricht, W. A. Richards, B. D. Richards, M. P. Cosimano, M. A. Klinedinst, J. Psychopharmacol. 2016, 30, 1181-1197.
    1. R. L. Carhart-Harris, M. Bolstridge, J. Rucker, C. M. J. Day, D. Erritzoe, M. Kaelen, M. Bloomfield, J. A. Rickard, B. Forbes, A. Feilding, D. Taylor, S. Pilling, V. H. Curran, D. J. Nutt, The Lancet Psychiatry 2016, 3, 619-627.

Publication types

MeSH terms

Substances

Grants and funding

LinkOut - more resources

Full text links
Wiley full text link Wiley
Cite
Send To

NCBI Literature Resources

MeSHPMCBookshelfDisclaimer

The PubMed wordmark and PubMed logo are registered trademarks of the U.S. Department of Health and Human Services (HHS). Unauthorized use of these marks is strictly prohibited.


[8]ページ先頭

©2009-2025 Movatter.jp