N-Acetyltryptamine
Appearance
(Redirected from N-acetyltryptamine)
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Names | |
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IUPAC name
N-[2-(1H-indol-3-yl)ethyl]acetamide[1]
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Other names
Acetotryptamide
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChEMBL | |
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PubChem CID
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CompTox Dashboard (EPA)
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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).
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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
[edit]- ^ "N-Acetyltryptamine". pubchem.ncbi.nlm.nih.gov.
- ^ O'Brien, Paul (2 December 2012). Pineal and Retinal Relationships. Elsevier. p. 159. ISBN 978-0-323-14985-3.
- ^ 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.
- ^ "N-Acetyltryptamine (N10-Acetyltryptamine) | Melatonin Receptor Agonist | MedChemExpress". MedchemExpress.com.
- ^ 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. PMC 6270429.
- ^ Paley, Elena L. (8 October 2020). Protein Biosynthesis Interference in Disease. Academic Press. p. 94. ISBN 978-0-12-823486-0.
Further reading
[edit]- Houlihan, William J. (15 September 2009). Indoles, Volume 25, Part 2. John Wiley & Sons. p. 25. ISBN 978-0-470-18841-5.