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

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2002 Spring;8(1):90-100.
doi: 10.1111/j.1527-3458.2002.tb00217.x.

SB-258741: a 5-HT7 receptor antagonist of potential clinical interest

Affiliations
Review

SB-258741: a 5-HT7 receptor antagonist of potential clinical interest

Bruno Pouzet. CNS Drug Rev. 2002 Spring.

Abstract

Recently, a series of 5-HT7 receptor antagonists have been developed (24,29,36,68). Among them SB-258741, R-(+)-1-(toluene-3-sulfonyl)-2-[2-(4-methylpiperidin-1-yl)ethyl]-pyrrolidine, (compound "13" in 36,37) was one of the most potent and specific compounds. Due to a lack of specific ligands the pharmacology of 5-HT7 receptor antagonists is still relatively unexplored. It has been suggested, however, that 5-HT7 receptor ligands could be useful in the therapy of various disorders such as sleep disorders, schizophrenia, depression, migraine, epilepsy, pain, or memory impairment. Many of these conceivable indications are not supported by pharmacological data. It is, therefore, of particular interest to review the data generated from studies of one of these most potent and specific 5-HT7 receptor antagonists, SB-258741, with a goal of testing the validity of the proposed clinical indications. In this review, the author describes pharmacology of this compound in order to define its potential clinical use. The available safety pharmacology data are discussed in an attempt to predict potential side effects of specific 5-HT7 receptor antagonists.

PubMed Disclaimer

References

    1. Anderson WP, Evans RG, Malpas SC. Pressure natriuresis and long‐term blood pressure control. J Cardiovasc Pharmacol 1995;26 (Suppl 2): S17–S23. - PubMed
    1. Arnt J. Pharmacological specificity of conditioned avoidance response inhibition in rats: inhibition by neuroleptics and correlation to dopamine receptor blockade. Acta pharmacologica et toxicologica 1982;51:321–329. - PubMed
    1. Arnt J. Differential effects of classical and newer antipsychotics on the hypermotility induced by two dose levels of D‐amphetamine. Eur J Pharmacol 1995;283:55–62. - PubMed
    1. Arnt J. Screening models for antipsychotic drugs In: Ellenbroek BA, Cools AR, Eds. Atypical antipsychotics. Basel : Bikhäuser, 2000:99–119.
    1. Arnt J, Skarsfeldt T. Do novel antipsychotics have similar pharmacological characteristics? A review of the evidence. Neuropsychopharmacology 1998;18:63–101. - PubMed

MeSH terms

LinkOut - more resources