Selectivity of 4-methoxyphenethylamine derivatives as inhibitors of monoamine oxidase
β Scribed by William J. Keller; Gary G. Ferguson
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- English
- Weight
- 259 KB
- Volume
- 65
- Category
- Article
- ISSN
- 0022-3549
No coin nor oath required. For personal study only.
β¦ Synopsis
in the analysis of the isoniazid-pyridoxine hydrochloride (101) mixture is clearly demonstrated, with an accuracy of 0.17-0.3096.
REFERENCES
(1) I.
π SIMILAR VOLUMES
Prodrugs of Neuron-Selective Monoamine Oxidase Inhibitors: Amino Acid Derivatives of 1-(4-Aminophenyl)-2-aminopropanes. -The most interesting derivative within this series is found to be glycine amide (VII). It is shown that amino acid derivatives show only weak MAO inhibitory activity in vitro but
The cactus alkaloid 3,4-dimethoxyphenethylamine and its naturally occurring N-methylated homologs inhibited the deamination of tyramine and tryptamine by rat brain monoamine oxidase. In contrast, the beta-hydroxylated derivatives of this series failed to inhibit the action of monoamine oxidase on bo
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract New indolylβ1,3,4βoxadiazole and oxadiazine derivatives were prepared as reversible monoamine oxidase inhibitors. The compound 5β(3βmethylindolyl)β1,3,4βoxadiazolβ2(3__H__)one was shown to be a good monoamine oxidase B inhibitor.