(R)(+)-N-propargyl-1-aminoindan (rasagiline) and derivatives: highly selective and potent inhibitors of monoamine oxidase B.

Article Details

Citation

Sterling J, Veinberg A, Lerner D, Goldenberg W, Levy R, Youdim M, Finberg J

(R)(+)-N-propargyl-1-aminoindan (rasagiline) and derivatives: highly selective and potent inhibitors of monoamine oxidase B.

J Neural Transm Suppl. 1998;52:301-5.

PubMed ID
9564630 [ View in PubMed
]
Abstract

(+)-N-Propargyl-1-aminoindan (rasagiline) and a series of derivatives have been synthesized and screened for monoamine oxidase inhibitory activity. Rasagiline and several analogues were found be highly selective and potent inhibitors of the B form of the enzyme in contrast to the levorotatory enantiomer which was not active. The results indicate that rasagiline has potential for the treatment of Parkinson's Disease. This compound is currently under development for that indication.

DrugBank Data that Cites this Article

Drug Targets
DrugTargetKindOrganismPharmacological ActionActions
N-Propargyl-1(S)-AminoindanAmine oxidase [flavin-containing] BProteinHumans
Unknown
Inhibitor
Details
Drug Enzymes
DrugEnzymeKindOrganismPharmacological ActionActions
N-Propargyl-1(S)-AminoindanAmine oxidase [flavin-containing] BProteinHumans
Unknown
Inhibitor
Details