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Inhibition of monoamine oxidase by the R and S enantiomers of N-N-methyl-3-butyn-2-amine

DOI: 10.1016/0223-5234(92)90059-A

Source and publish data:

European Journal of Medicinal Chemistry p. 45 - 52 (1992)

Update date:2022-08-03

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Authors:

Dostert, PDostert, P

O'Brien, EMO'Brien, EM

Tipton, KFTipton, KF

Meroni, MMeroni, M

Melloni, PMelloni, P

Benedetti, M StrolinBenedetti, M Strolin

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Article abstract of DOI:10.1016/0223-5234(92)90059-A

The chemical synthesis of the R-(+)- and S-(-)-enantiomers of N<3-(2,4-dichlorophenoxy)propyl>-N-methyl-3-butyn-2-amine is described.These compounds are derivatives of the mechanism-based irreversible monoamine oxidase inhibitor clorgyline in which a meth

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Full text of DOI:10.1016/0223-5234(92)90059-A

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Product name:R-(+)-N<3-(2,4-dichlorophenoxy)propyl>-N-methyl-3-butyn-2-amine

Cas No:141625-61-8

141625-61-8

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