Results 161 to 170 of about 7,416 (225)
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N-Alkylation of phenethylamine and tryptamine

Bioorganic & Medicinal Chemistry Letters, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
Gerta, Cami-Kobeci   +3 more
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Preparation of 13N-β-phenethylamine

The International Journal of Applied Radiation and Isotopes, 1985
Nitrogen-13-labelled beta-phenethylamine[( 13N]PEA) was synthesized by Hofmann rearrangement of [13N]phenylpropionamide prepared from phenylpropionyl chloride and aqueous [13N]ammonia solution. The reaction proceeded rapidly with a fairly good yield. [13N]PEA was isolated using preparative thin-layer chromatography, and organ distribution in mice was ...
T, Tominaga   +5 more
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New phenethylamines in Europe

Drug Testing and Analysis, 2013
Sixteen phenethylamines are now included in Schedules I and II of the United Nations 1971 Convention on Psychotropic Substances. Most of the ring‐substituted compounds are in Schedule I, whereas 2C‐B, amphetamine, and methamphetamine are listed in Schedule II. Substances in Schedule IV (e.g.
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Fluorine in psychedelic phenethylamines

Drug Testing and Analysis, 2012
The so‐called psychedelic phenethylamines represent a class of drugs with a large range of psychoactive properties in humans, ranging from naturally occurring mescaline to amphetamine analogues and homologues. The interest in many of these compounds, occasionally referred to as designer‐drugs, is widely dispersed across popular culture and political ...
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Chemistry of Phenethylamines Related to Mescaline

Journal of Psychedelic Drugs, 1979
(1979). Chemistry of Phenethylamines Related to Mescaline. Journal of Psychedelic Drugs: Vol. 11, Innovative Approached to Drug Abuse Treatment, pp. 41-52.
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Serotonergic properties of β-phenethylamine in rats

Neuropharmacology, 1980
Current research interest in β-phenethylamine (PEA) derives, in part, from a possible role for this endogenous compound in paranoid schizophrenia. Systemic administration of PEA caused a behavioral syndrome in rats (simultaneous forepaw padding, side-to-side headweaving or head tremor and splayed hindlimbs) which reflects activation of serotonin (5-HT)
R S, Sloviter, J D, Connor, E G, Drust
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Conformational analysis of some phenethylamine molecules

Journal of Theoretical Biology, 1973
Abstract A set of empirical potential functions (EPF), previously used in conformational energy calculations of polymers, was employed in the study of the conformational properties of a number of methyl-substituted phenethylmines, as well as phenylmethylamine, phenyl- n -propylamine, and 3,4,5-trimethoxyamphetamine. The conformational free energy was
H J, Weintraub, A J, Hopfinger
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The stereoselective inhibition of lipolysis by nonphenolic phenethylamines

European Journal of Pharmacology, 1974
Abstract Inhibition of norepinephrine-induced lipolysis by the steroisomers of ephedrine and phenyl-2-piperidyl carbinol and the diastereomers of 8-hydroxy-6,7-benzomorphan was investigated in rat adipose tissue, in vitro. Relative inhibitory actions of stereoisomers were observed to be 1R,2S > 1S,2R = 1R,2R = 1S,2S.
J J, Fauley, D R, Feller, J B, LaPidus
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2,3-Dihydrobenzofuran analogs of hallucinogenic phenethylamines

Journal of Medicinal Chemistry, 1991
Two 2,3-dihydrobenzofuran analogues of hallucinogenic amphetamines were prepared and evaluated for activity in the two-lever drug-discrimination paradigm in rats trained to discriminate saline from LSD tartrate (0.08 mg/kg) and for the ability to displace [125I]-(R)-DOI [( 125I]-(R)-1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane) from rat cortical ...
D E, Nichols   +4 more
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Centrally active phenethylamines.

Psychopharmacology communications, 1976
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 ...
A T, Shulgin, M F, Carter
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