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Amphetamine derivatives as Monoamine Oxidase Inhibitors
(Frontiers Media, 2020)
Amphetamine and its derivatives exhibit a wide range of pharmacological activities, including psychostimulant, hallucinogenic, entactogenic, anorectic, or antidepressant effects. The mechanisms of action underlying these ...
Amphetamine derivatives as monoamine oxidase inhibitors
(Frontiers Media S.A., 2020)
Naphthylisopropylamine and N-benzylamphetamine derivatives as monoamine oxidase inhibitors
(Elsevier Ltd., 2009-02-08)
A series of naphthylisopropylamine and N-benzyl-4-methylthioamphetamine derivatives were evaluated
as monoamine oxidase inhibitors. Their potencies were compared with those of a series of amphetamine
derivatives, to test ...
2-Arylthiomorpholine derivatives as potent and selective monoamine oxidase
(ELSEVIER, 2010)
2-Arylthiomorpholine and 2-arylthiomorpholin-5-one derivatives, designed as rigid and/or non-basic
phenylethylamine analogues, were evaluated as rat and human monoamine oxidase inhibitors. Molecular
docking provided ...
Monoamine Oxidase Inhibition In the Light of New Structural Data
(Bentham Science Publishers Ltd., 2004-11-25)
The recent description of the crystal structures of rat MAO-A and human MAO-B provides an
unprecedented framework to elucidate the mechanisms underlying the selective interactions between these
proteins and their ligands. ...
Monoamine Oxidase Inhibitory Properties of Some Methoxylated and Alkylthio Amphetamine Derivatives STRUCTURE-ACTIVITY RELA TIONSHIPS
(Elsevier Science Inc., 1997)
The monoamine oxidase (MAO) inhibitory propenies of a series of amphetamine derivatives
with difTerent substituents at or around rhe para position of the aromaric ring were evaluateJ. i¡, in viero stuJies
in which a crude ...
Monoamine oxidase inhibitory properties of some methoxylated and alkylthio amphetamine derivatives. Structure-activity relationships
(1997)
The monoamine oxidase (MAO) inhibitory properties of a series of amphetamine derivatives with different substituents at or around the para position of the aromatic ring were evaluated. In in vitro studies in which a crude ...