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A preliminary investigation of the psychoactive agent 4-bromo-2,5-dimethoxyphenethylamine: a potential drug of abuse.

Richard A Glennon, M Titeler, R A Lyon

Pharmacology, biochemistry, and behavior July 1988 DOI: 10.1016/0091-3057(88)90071-8 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Preclinical pharmacological study Peer reviewed
Population Rats
Interventions 4-Bromo-2 5-dimethoxyphenethylamine (alpha-desMe DOB)
Key points Alpha-desMe DOB binds with high affinity to 5-HT2 serotonin receptors (Ki = 1 nM) but, unlike DOB, also binds to 5-HT1A, 5-HT1B, and 5-HT1C receptors, making it less selective. In drug discrimination studies, it produced stimulus generalization in rats trained to discriminate DOM or R(-)DOB from saline, though with extensive behavioral disruption. The authors tentatively conclude it is a psychoactive agent with at least some hallucinogenic or DOB-like properties.

Abstract

4-Bromo-2,5-dimethoxyphenethylamine (alpha-desMe DOB) is a psychoactive agent that may possess significant abuse potential. Because of its structural similarity to the established hallucinogen 1-(4-bromo-2,5-dimethoxyphenyl)-2-aminopropane (DOB), and because almost no pharmacological data are available on this agent, we undertook this preliminary investigation. alpha-DesMe DOB (Ki = 1 nM), like DOB itself (Ki = 0.79 nM), displays a high affinity for [3H]DOB-labeled central 5-HT2 serotonin receptors. However, unlike DOB, the alpha-desmethyl derivative also binds with significant affinity to 5-HT1A, 5-HT1B, and 5-HT1C serotonin receptors and, as such, is less selective than DOB. In drug discrimination studies using rats trained to discriminate either DOM (i.e., the 4-methyl analog of DOB) or R(-)DOB from saline, stimulus generalization occurred in both groups of animals. However, stimulus generalization was associated with extensive disruption of behavior, alpha-DesMe DOB may produce stimulus effects similar, but not identical, to those of DOM and R(-)DOB; in addition, this agent may be capable of producing other, as yet undefined, central effects at comparable doses. These other effects may be reflective of the lack of selectivity of alpha-desMe DOB for 5-HT2 serotonin receptors. Because other hallucinogenic agents display high affinity for 5-HT2 serotonin receptors and result in stimulus generalization in DOM- and/or DOB-trained animals, it is tentatively concluded that alpha-desMe DOB is a psychoactive agent with at least some hallucinogenic or DOB-like properties.