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Shulgin AT, Carter MF. 
“Centrally Active Phenethylamines”. 
Psychopharmacology Communications. 1975;1(1):93-98.
The two-carbon homologs of two potent psychotomimetic agents are described. Unlike the parent isopropylamine compounds (4-methyl-2,5-dimethoxyamphetamine, DOM, STP; and 4-bromo-2,5-dimethoxyamphetamine, PBR, 4-BR) these phenethylamines lead to an intoxication state which is, in normal subjects, of short duration and of greatly increased sensory enhancement, but which does not super impose hallucinogenesis. These two phenethylamines, 4-methl-2,5-dimethoxyphenethylamine (II) and 4-bromo-2,5-dimethoxyphenthylamine (III), are active in man at oral levels of 0.1 to 0.2 mg/Kg, approximately one tenth the potency of their three-carbon counterparts.
Notes # : 2C-B
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