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Deprenyl
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Deprenyl, also known by its developmental code name E-250 and as N-propargylmethamphetamine, is the of and (selegiline).

(1993). 9783034863490, Birkhäuser Basel.
It was discovered in 1961 in at by Zoltan Ecseri and József Knoll, was patented in 1962, and was first described in the literature in 1964 or 1965.

The drug is a monoamine oxidase inhibitor and norepinephrine–dopamine releasing agent. It is a of and , which mediates the latter action. Deprenyl was studied clinically at high doses of 50 to 100mg/day and was described as a and . At lower doses, selective would be expected, but at these higher doses, dual inhibition of and MAO-B would occur, on the basis of L-deprenyl.

Subsequent to its synthesis, the of deprenyl were separated. The isomer, D-deprenyl, was found to be more , producing effects like and more potent psychostimulation in rodents. The isomer, selegiline, was much more potent as an , and was subsequently developed for the treatment of Parkinson's disease and depression.

Deprenyl is reported to result in including agitation, , and sleep disturbances more often than selegiline.

Similarly to selegiline, deprenyl is a catecholaminergic activity enhancer (CAE). Both of deprenyl, D-deprenyl and selegiline, are active in this respect, but selegiline is slightly more potent than D-deprenyl.


See also
  • Substituted amphetamine
  • 4-Fluorodeprenyl
  • AGN-1135 (racemic rasagiline)
  • SU-11739 (racemic N-methylated rasagiline)

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