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N-methylserotonin

chemical compound
ChemicalSubstance type_of_chemical_entity Q855403
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N-methylserotonin

Summary

N-methylserotonin is a type of chemical entity[1]. N-methylserotonin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (18 views/month).[2]

Key Facts

  • N-methylserotonin's instance of is recorded as type of chemical entity[3].
  • N-methylserotonin's chemical structure is recorded as Norbufotenine.svg[4].
  • N-methylserotonin's CAS Registry Number is recorded as 1134-01-6[5].
  • N-methylserotonin's canonical SMILES is recorded as CNCCC1=CNC2=C1C=C(C=C2)O[6].
  • N-methylserotonin's InChI is recorded as InChI=1S/C11H14N2O/c1-12-5-4-8-7-13-11-3-2-9(14)6-10(8)11/h2-3,6-7,12-14H,4-5H2,1H3[7].
  • N-methylserotonin's InChIKey is recorded as ASUSBMNYRHGZIG-UHFFFAOYSA-N[8].
  • N-methylserotonin's chemical formula is recorded as C₁₁H₁₄N₂O[9].
  • N-methylserotonin's subclass of is recorded as tryptamine alkaloid[10].
  • N-methylserotonin's ChEMBL ID is recorded as CHEMBL277362[11].
  • N-methylserotonin's Freebase ID is recorded as /m/0kg37st[12].
  • N-methylserotonin's UNII is recorded as MZ25L5SJ6Z[13].
  • N-methylserotonin's ChemSpider ID is recorded as 132989[14].
  • N-methylserotonin's PubChem CID is recorded as 150885[15].
  • N-methylserotonin's KEGG ID is recorded as C06212[16].
  • N-methylserotonin's ChEBI ID is recorded as 48294[17].
  • N-methylserotonin's found in taxon is recorded as Homo sapiens[18].
  • N-methylserotonin's found in taxon is recorded as Amanita citrina[19].
  • N-methylserotonin's found in taxon is recorded as common toad[20].
  • N-methylserotonin's found in taxon is recorded as Asiatic toad[21].
  • N-methylserotonin's found in taxon is recorded as Phyllodium pulchellum[22].
  • N-methylserotonin's found in taxon is recorded as tomato[23].
  • N-methylserotonin's Reaxys registry number is recorded as 145589[24].
  • N-methylserotonin's Human Metabolome Database ID is recorded as HMDB0004369[25].
  • N-methylserotonin's KNApSAcK ID is recorded as C00051736[26].
  • N-methylserotonin's mass is recorded as {'unit': 'Q483261', 'amount': '+190.110613'}[27].

Why It Matters

N-methylserotonin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (18 views/month).[2]

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] ↑ . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . PubChem. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . ChEMBL. Retrieved . wikidata.org.
  10. [12] ↑ . Freebase Data Dumps. wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . Q2311683. Retrieved . wikidata.org.
  13. [15] ↑ . PubChem. Retrieved . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . ChEBI. Retrieved . wikidata.org.
  16. [18] ↑ . Recon 2.2: from reconstruction to model of human metabolism. wikidata.org.
  17. [19] ↑ . INVESTIGATION OF THE ALKALOIDS OFAMANITASPECIES1– II.AMANITA. CITRINAANDAMANITA PORPHYRIA. wikidata.org.
  18. [20] ↑ . Quality evaluation of traditional Chinese drug toad venom from different origins through a simultaneous determination of bufogenins and indole alkaloids by HPLC.. wikidata.org.
  19. [21] ↑ . Quality evaluation of traditional Chinese drug toad venom from different origins through a simultaneous determination of bufogenins and indole alkaloids by HPLC.. wikidata.org.
  20. [22] ↑ . Chemical and pharmacological evaluation of Desmodium pulchellum. wikidata.org.
  21. [23] ↑ . Biosynthesis and Metabolism of Indol-3yl-acetic Acid. wikidata.org.
  22. [24] ↑ . ChEBI. Retrieved . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . PubChem. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.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-methylserotonin. Retrieved May 3, 2026, from https://4ort.xyz/entity/n-methylserotonin
MLA “N-methylserotonin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/n-methylserotonin.
BibTeX @misc{4ortxyz_n-methylserotonin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{N-methylserotonin}}, year = {2026}, url = {https://4ort.xyz/entity/n-methylserotonin}, note = {Accessed: 2026-05-03}}
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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 25d ago · Shuaib-bot bot · 2026-05-01 view diff on Wikidata ↗
    Subclass of → tryptamine alkaloid
    Found in taxon → Homo sapiens, Amanita citrina, common toad +3
    Mass → {'unit': 'Q483261', 'amount': '+190.110613'}
    Instance of → —
    + 3 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-and-other-short:0||ur */"
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