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Candace B Johnson

Department of Psychology, Western Michigan University, Kalamazoo, Michigan (C.B.J., L.E.B.); Designer Drug Research Unit, National Institute on Drug Abuse Intramural Research Program, Baltimore, Maryland (D.W., M.H.B.); and Tactogen Inc., Palo Alto, California (M.J.B.).

1 paper in the library · 5 citations · publishing 2024

Papers

Novel Benzofuran Derivatives Induce Monoamine Release and Substitute for the Discriminative Stimulus Effects of 3,4-Methylenedioxymethamphetamine.

The Journal of pharmacology and experimental therapeutics September 18, 2024 Candace B Johnson, Donna Walther, Matthew J Baggott et al. 5 citations

MDMA is effective as a treatment for PTSD but carries cardiovascular and neurological risks. Researchers tested two new compounds, 5-MABB and 6-MABB, in rat brain tissue and in live rats trained to recognize MDMA. The S isomers of both compounds released serotonin, norepinephrine, and dopamine, similar to MDMA. The R isomers released serotonin and partially released norepinephrine but not dopamine. All compounds caused rats to respond as if they had received MDMA, with effects increasing with dose. The R isomers were less potent behaviorally. The findings suggest the aminoalkyl benzofuran structure is a promising starting point for developing safer MDMA-like drugs.