Pharmacological characterization of two novel and potent 5-HT4 receptor agonists, RS 67333 and RS 67506, in vitro and in vivo

Author:

Eglen R.M.,Bonhaus D.W.,Johnson L.G.,Leung E.,Clark R.D.

Publisher

Wiley

Subject

Pharmacology

Reference27 articles.

1. Quaternised renzapride as a potent and selective 5-HT4 receptor agonist;BAXTER;BioOrgan hem Letts.,1993

2. 5-Hydroxytryptamine4 receptors mediate relaxation of the rat oesophageal tunica muscularis mucosae;BAXTER;Naunyn-Schmied. Arch. Pharmacol.,1991

3. 5-HT4 receptors: potential therapeutic implications in neurology and psychiatry;BOCKAERT;CNS Drugs,1994

4. [3H] RS 23597-190, a potent 5-hydroxytryptamine4 antagonist labels sigma-1 but not sigma2 binding sites in guinea-pig brain;BONHAUS;J. Pharmacol. Exp. Ther.,1994

5. Relationship between inhibitor constant (Ki) and the concentration of inhibitor which causes 50 percent inhibition (IC50) of an enzymatic reaction;CHENG;Biochem. Pharmacol.,1973

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