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J 508

Known as: J-508 
 
National Institutes of Health

Papers overview

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2008
2008
  • Ildikó Miklya
  • Neuropsychopharmacologia Hungarica : a Magyar…
  • 2008
  • Corpus ID: 25946300
N-methylpropargylamine-1-aminoindane (J-508), a strong releaser of catecholamines was described 30 years ago as a more potent… Expand
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2005
2005
  • Jozsef Knoll
  • Journal of Neural Transmission
  • 2005
  • Corpus ID: 40734694
(-)Deprenyl, a selective inhibitor of MAO-B, was found to be 60 times less potent in inhibiting intestinal MAO in the rat than… Expand
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2000
2000
The noradrenaline (NA), dopamine (DA) and serotonin (5HT) reuptake inhibitory potency of deprenyl, the highly selective and… Expand
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Review
1994
Review
1994
  • Kálmán Magyar
  • Journal of neural transmission. Supplementum
  • 1994
  • Corpus ID: 35028287
A number of new deprenyl analogues were synthesized during the last decades and structure-activity relationship studies were… Expand
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1990
1990
Serum binding, the effect on striatal dopamine release and the metabolism of (-)-deprenyl [N-methyl-N-propargyl(2-phenyl-1-methyl… Expand
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1989
1989
The concentrations of monoamine oxidase-A and -B were determined in homogenates of human cerebral cortex, caudatus and placenta… Expand
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1986
1986
The concentrations of monoamine oxidase-A and -B have been determined in mitochondria, mitochondrial outer membranes and… Expand
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1982
1982
The effects of single doses of (-)deprenyl, in comparison to J-508, U-1424, pargyline and clorgyline, on the sexual performance… Expand
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1979
1979
Abstract Rats were treated subcutaneously with different doses of the “B form” selective monoamine oxidase (MAO) inhibitors… Expand
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1979
1979
The interaction between rat brain monoamine oxidase-B and J-508, an analogue of L-deprenil, has been investigated. J-508 inhibits… Expand
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