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N-acetylserotonin

chemical compound
ChemicalSubstance type_of_chemical_entity Q4847704
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N-acetylserotonin

Summary

N-acetylserotonin is a type of chemical entity[1]. N-acetylserotonin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (33 views/month).[2]

Key Facts

  • N-acetylserotonin's instance of is recorded as type of chemical entity[3].
  • N-acetylserotonin's chemical structure is recorded as N-acetylserotonin.svg[4].
  • N-acetylserotonin's CAS Registry Number is recorded as 1210-83-9[5].
  • N-acetylserotonin's EC number is recorded as 214-916-5[6].
  • N-acetylserotonin's canonical SMILES is recorded as CC(=O)NCCC1=CNC2=C1C=C(C=C2)O[7].
  • N-acetylserotonin's InChI is recorded as InChI=1S/C12H14N2O2/c1-8(15)13-5-4-9-7-14-12-3-2-10(16)6-11(9)12/h2-3,6-7,14,16H,4-5H2,1H3,(H,13,15)[8].
  • N-acetylserotonin's InChIKey is recorded as MVAWJSIDNICKHF-UHFFFAOYSA-N[9].
  • N-acetylserotonin's chemical formula is recorded as C₁₂H₁₄N₂O₂[10].
  • N-acetylserotonin's subclass of is recorded as tryptamine alkaloid[11].
  • N-acetylserotonin's part of is recorded as acetylserotonin O-methyltransferase activity[12].
  • N-acetylserotonin's Commons category is recorded as N-Acetylserotonin[13].
  • N-acetylserotonin's MeSH descriptor ID is recorded as C006389[14].
  • N-acetylserotonin's ChEMBL ID is recorded as CHEMBL33103[15].
  • N-acetylserotonin's Guide to Pharmacology Ligand ID is recorded as 5451[16].
  • N-acetylserotonin's PDB structure ID is recorded as 4A6E[17].
  • N-acetylserotonin's PDB structure ID is recorded as 1NAS[18].
  • N-acetylserotonin's Freebase ID is recorded as /m/02rb1q0[19].
  • N-acetylserotonin's UNII is recorded as P4TO3C82WV[20].
  • N-acetylserotonin's ChemSpider ID is recorded as 879[21].
  • N-acetylserotonin's PubChem CID is recorded as 903[22].
  • N-acetylserotonin's KEGG ID is recorded as C00978[23].
  • N-acetylserotonin's ChEBI ID is recorded as 17697[24].
  • N-acetylserotonin's found in taxon is recorded as Homo sapiens[25].
  • N-acetylserotonin's found in taxon is recorded as Caenorhabditis elegans[26].
  • N-acetylserotonin's found in taxon is recorded as common sunflower[27].

Why It Matters

N-acetylserotonin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (33 views/month).[2] N-acetylserotonin has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[28] N-acetylserotonin is known by 8 alternative names across languages and contexts.[29]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . ChEMBL. Retrieved . wikidata.org.
  14. [16] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  15. [17] ↑ . Protein Data Bank. Retrieved . wikidata.org.
  16. [18] ↑ . Protein Data Bank. Retrieved . wikidata.org.
  17. [19] ↑ . Freebase Data Dumps. wikidata.org.
  18. [20] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  19. [21] ↑ . Q2311683. Retrieved . wikidata.org.
  20. [22] ↑ . PubChem. Retrieved . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . ChEBI. Retrieved . wikidata.org.
  23. [25] ↑ . Recon 2.2: from reconstruction to model of human metabolism. wikidata.org.
  24. [26] ↑ . Modeling Meets Metabolomics-The WormJam Consensus Model as Basis for Metabolic Studies in the Model Organism. wikidata.org.
  25. [27] ↑ . Salt stress‐induced seedling growth inhibition coincides with differential distribution of serotonin and melatonin in sunflower seedling roots and cotyledons. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] ↑ . Wikidata sitelinks. wikidata.org.
  3. [29] ↑ . Wikidata aliases. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). N-acetylserotonin. Retrieved May 3, 2026, from https://4ort.xyz/entity/n-acetylserotonin
MLA “N-acetylserotonin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/n-acetylserotonin.
BibTeX @misc{4ortxyz_n-acetylserotonin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{N-acetylserotonin}}, year = {2026}, url = {https://4ort.xyz/entity/n-acetylserotonin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): N-acetylserotonin — https://4ort.xyz/entity/n-acetylserotonin (retrieved 2026-05-03)

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