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N-Methyl-benzylamine, a metabolite of pargyline in man.

✍ Scribed by R Pirisino; GB Ciottoli; F Buffoni; B Anselmi; C Curradi


Book ID
117941996
Publisher
John Wiley and Sons
Year
1979
Tongue
English
Weight
445 KB
Volume
7
Category
Article
ISSN
0306-5251

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πŸ“œ SIMILAR VOLUMES


Synthesis and pharmacology of a pargylin
✍ Jerome F. Siuda; Carole Cihonski; R. Duane Sofia; Joseph P. Buckley πŸ“‚ Article πŸ“… 1973 πŸ› John Wiley and Sons 🌐 English βš– 244 KB

The synthesis of a structural isomer of pargyline was undertaken to test certain structure-activity relationships. I n uioo, the new compound, N-34 1-butyny1)-benzylamine. exhibited slight central stimulant effects but showed no MA0 inhibitory activity in uitro. Keyphrases 0 N-3-(l-Butynyl)-benzyla

Synthesis of [14C]-pargyline {N-methyl-N
✍ David J. W. Goon; James A. Elberling; E. G. Demaster; Herbert T. Nagasawa πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 French βš– 245 KB

## Abstract A one‐pot reaction scheme leading to ^14^C‐labeled pargyline (N‐methyl‐N‐ propargylbenzylamine) where in the radioactive label from [^14^C]‐formaldehyde is synthetically incorporated into the methylene group of the propargyl side chain is described. Thus, [^14^C]‐formaldehyde (aqueous s