6-Hydroxylation: An important metabolic route for α-methyltryptamine

@article{Szra20056HydroxylationAI,
  title={6-Hydroxylation: An important metabolic route for $\alpha$-methyltryptamine},
  author={St. Sz{\'a}ra},
  journal={Experientia},
  year={2005},
  volume={17},
  pages={76-76}
}
  • S. Szára
  • Published 15 February 1961
  • Biology
  • Experientia
Der Stoffwechsel der psychotropischen Verbindung α-Methyltryptamin wurde untersucht. Die drei hauptsächlichsten Metabolite wurdenin vitro undin vivo als 6-Hydroxy-α-methyltryptamin, 3-Indolylaceton und 6-Hydroxy-3-indolylaceton identifiziert. 

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References

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Hydroxylation and N-demethylation of N,N-dimethyltryptamine

TLDR
An weiteren Stoffwechselprodukten wurden nachgewiesen: N,N-Dimethyltryptamin-N-oxyd und sein 6-Hydroxy-Derivat (in vitro), sowie Tryptamin, Indol-3-essigsäure und 6-hydroxyindol- 3-essigäure (in vivo).

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