CHEMICAL STRUCTURE | ![]() |
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DRUG CLASS | SELECTIVE MAO-B INHIBITOR / PROTOPSYCHOSTIMULANT |
MECHANISMS OF ACTION |
IRREVERSIBLE MONOAMINE OXIDASE-B INHIBITION (MAO-B) INCREASES SYNAPTIC DOPAMINE, PHENYLETHYLAMINE (PEA), AND TYRAMINE LEVELS AT HIGHER DOSES, EXHIBITS NON-SELECTIVE MAO INHIBITION AND STIMULANT EFFECTS TRACE AMINE RECEPTOR (TAAR1) INTERACTION SUSPECTED |
MONOGRAPH |
CHEMICAL NAME: (2S)-N-methyl-1-phenyl-N-prop-2-ynyl-propan-2-amine DEVELOPMENT: INTRODUCED IN 1960S AS AN ANTIDEPRESSANT, NOW USED IN PARKINSON'S DISEASE AT LOW DOSES, ENHANCES DOPAMINERGIC TONE IN SUBCORTICAL BRAIN REGIONS AT HIGH DOSES, CAUSES PSYCHOSTIMULANT-LIKE EFFECTS DUE TO MAO-A INHIBITION AND INCREASED PEA MODERN INTEREST: ENTHEODELIC POTENTIAL IN LOW-DOSE MICROSTACKS. A VINTAGE MONOAMINE NOW REINTERPRETED BY PSYCHOPHARMACEUTICAL THEORISTS. STRUCTURAL NOTES: CONTAINS PROPYNYLAMINE CHAIN → ALKYNE-BEARING MAO INHIBITORS MAY FORM IRREVERSIBLE COVALENT BONDS |
SYNTHESIS BATCH INITIATED | 300 MILIGRAMS TARGET | AMOUNT ACQUIRED FOR SYNTHESIS PURPOSES: 300 MG | AMOUNT ACQUIRED FOR SPECULATIVE HOLDING: 0 MG NOTE: THESE FIGURES REFLECT TOTAL DOCUMENTED ACQUISITIONS. UPDATED MANUALLY |
ORDER BOOK |
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ORDER VIA | (ONLY TO EUROPE, EXCEPT UK, DENMARK, AND AUSTRIA.) |