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Presence of N-methyldopamine in parkinsonian and normal human brains.

Abstract
N-Methyldopamine (epinine) has been identified for the first time in parkinsonian and normal human brains by gas chromatography-mass spectrometry. N-Methylsalsolinol and N-methylnorsalsolinol, which are analogues of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine, which produces parkinsonism in humans, may be synthesized from N-methyldopamine by the Pictet-Spengler condensation reaction as an alternative metabolic pathway.
AuthorsM Kajita, T Niwa, N Takeda, H Yoshizumi, A Tatematsu, K Watanabe, T Nagatsu
JournalJournal of chromatography (J Chromatogr) Vol. 613 Issue 1 Pg. 1-8 (Mar 05 1993) Netherlands
PMID8458887 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Isoquinolines
  • Salsoline Alkaloids
  • Tetrahydroisoquinolines
  • 2-methyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline
  • salsoline
  • Deoxyepinephrine
Topics
  • Brain (metabolism)
  • Deoxyepinephrine (metabolism)
  • Gas Chromatography-Mass Spectrometry
  • Humans
  • Isoquinolines (metabolism)
  • Parkinson Disease (metabolism)
  • Salsoline Alkaloids (metabolism)
  • Tetrahydroisoquinolines

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