Structure-activity relationships in potentially hallucinogenic N,N-dialkyltryptamines substituted in the benzene moiety
作者:Toni B. Kline、Frederick Benington、Richard D. Morin、John M. Beaton
DOI:10.1021/jm00350a005
日期:1982.8
A series of N,N-dialkyltryptamines with methylthio or methylenedioxy substituents in the 4, 5, and 6 positions and methyl or isopropyl on the side-chain nitrogen has been synthesized. The behavioral pharmacology of these compounds showed them to possess Bovet-Gatti profiles characteristic of hallucinogens, and the 5-methylthio congener was the most potent. Binding studies at [3H]LSD and [3H]5-HT sites demonstrated that no single structural feature correlated with binding or behavioral changes and suggest a complex mode of action for these potential hallucinogenic agents.
GROTJAHN, D. B., J. HETEROCYCL. CHEM., 1983, 20, N 4, 1031-1036
作者:GROTJAHN, D. B.
DOI:——
日期:——
Synthesis and characterization of 5<i>H</i>-1,3-dioxolo[4,5-<i>f</i>]indoleethylamines
作者:Douglas B. Grotjahn
DOI:10.1002/jhet.5570200438
日期:1983.7
Twelve new N, N-dialkylated-5, 6-methylenedioxytryptamines and N-cyclopropyl-5, 6-methylenedioxytrypt-amine were prepared as hybrids of known psychoactive phenylethylamines and tryptamines. Novel, more convenient syntheses of N-methyl- and N-benzylcyclopropylamine are described.