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Serotonin Receptor Binding Affinities of Several Hallucinogenic Phenylalkylamine and N,N-Dimethyltryptamine Analogues

Richard A. Glennon, Stephen M. Liebowitz, Elizabeth C. Mack

Journal of Medicinal Chemistry January 1, 1978 DOI: 10.1021/jm00206a022 via Elsevier

Summary

AI-generated from the abstract

Several hallucinogenic compounds related to phenylalkylamine and N,N-dimethyltryptamine bind to serotonin (5-HT) receptors in rat stomach tissue. The most behaviorally potent analogues tested—DOB, DOM, and 5-methoxy-N,N-dimethyltryptamine—showed high binding affinities, with pA2 values of 7.35, 7.12, and 7.08, respectively.

Study at a glance

Characteristics In vitro study Peer reviewed
Population Rat stomach fundus tissue
Citations 35
Key finding The most behaviorally potent analogues DOB, DOM, and 5-methoxy-N,N-dimethyltryptamine had high affinities (pA2 = 7.35, 7.12, and 7.08) for 5-HT receptors in the rat stomach fundus model.

Abstract

Hallucinogenic phenylalkylamine and N,N-dimethyltryptamine analogues are known to affect serotonergic systems both in vivo and in vitro. Using a rat stomach fundus model, the 5-HT receptor binding affinities of several of these analogues were determined and compared. The most behaviorally potent analogues examined, DOB, DOM, and 5-methoxy-N,N-dimethyltryptamine, were found to possess rather high affirmities (pA2 = 7.35, 7.12, and 7.08, respectively) for the 5-HT receptors of the model system.

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