Chemistry:N-Acetyltryptamine

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N-Acetyltryptamine
N-Acetyltryptamine.png
Names
IUPAC name
N-[2-(1H-indol-3-yl)ethyl]acetamide[1]
Other names
Acetotryptamide
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
Properties
C12H14N2O
Molar mass 202.257 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

N-Acetyltryptamine is an organic compound with the molecular formula C12H14N2O. It is a partial agonist for the melatonin receptors.[2][3][4] N-Acetyltryptamine is produced by Streptomyces djakartensis and other Streptomyces and Fusarium species.[5][6]

References

  1. "N-Acetyltryptamine" (in en). pubchem.ncbi.nlm.nih.gov. https://pubchem.ncbi.nlm.nih.gov/compound/N-Acetyltryptamine#section=3D-Conformer. 
  2. O'Brien, Paul (2 December 2012) (in en). Pineal and Retinal Relationships. Elsevier. p. 159. ISBN 978-0-323-14985-3. 
  3. (in en) Current Trends in Comparative Endocrinology: Proceedings of the Ninth International Symposium on Comparative Endocrinology, Hong Kong, 7-11 December 1981. Kent State University Press. ISBN 978-962-209-116-0. 
  4. "N-Acetyltryptamine (N10-Acetyltryptamine) | Melatonin Receptor Agonist | MedChemExpress". MedchemExpress.com. https://www.medchemexpress.com/n-acetyltryptamine.html. 
  5. Zhang, Wenjuan; Wei, Shaopeng; Zhang, Jiwen; Wu, Wenjun (1 March 2013). "Antibacterial Activity Composition of the Fermentation Broth of Streptomyces djakartensis NW35". Molecules 18 (3): 2763–2768. doi:10.3390/molecules18032763. 
  6. Paley, Elena L. (8 October 2020) (in en). Protein Biosynthesis Interference in Disease. Academic Press. p. 94. ISBN 978-0-12-823486-0. 

Further reading

  • Houlihan, William J. (15 September 2009) (in en). Indoles, Volume 25, Part 2. John Wiley & Sons. p. 25. ISBN 978-0-470-18841-5.