5-methoxytryptamine

chemical compound
ChemicalSubstance type_of_chemical_entity Q4352011
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5-methoxytryptamine

Summary

5-methoxytryptamine is a type of chemical entity[1]. 5-methoxytryptamine ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (218 views/month).[2]

Key Facts

  • 5-methoxytryptamine's instance of is recorded as type of chemical entity[3].
  • 5-methoxytryptamine's chemical structure is recorded as 5-methoxytryptamine.svg[4].
  • 5-methoxytryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 1B[5].
  • 5-methoxytryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 1D[6].
  • 5-methoxytryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 1E[7].
  • 5-methoxytryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 1F[8].
  • 5-methoxytryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 2A[9].
  • 5-methoxytryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 2C[10].
  • 5-methoxytryptamine's physically interacts with is recorded as 5 hydroxytryptamine (serotonin) receptor 4[11].
  • 5-methoxytryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 4[12].
  • 5-methoxytryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 6[13].
  • 5-methoxytryptamine's physically interacts with is recorded as 5-hydroxytryptamine (serotonin) receptor 7[14].
  • 5-methoxytryptamine's physically interacts with is recorded as 5-hydroxytryptamine receptor 7[15].
  • 5-methoxytryptamine's CAS Registry Number is recorded as 608-07-1[16].
  • 5-methoxytryptamine's EC number is recorded as 210-153-7[17].
  • 5-methoxytryptamine's canonical SMILES is recorded as COC1=CC2=C(C=C1)NC=C2CCN[18].
  • 5-methoxytryptamine's InChI is recorded as InChI=1S/C11H14N2O/c1-14-9-2-3-11-10(6-9)8(4-5-12)7-13-11/h2-3,6-7,13H,4-5,12H2,1H3[19].
  • 5-methoxytryptamine's InChIKey is recorded as JTEJPPKMYBDEMY-UHFFFAOYSA-N[20].
  • 5-methoxytryptamine's chemical formula is recorded as C₁₁H₁₄N₂O[21].
  • 5-methoxytryptamine's subclass of is recorded as tryptamine alkaloid[22].
  • 5-methoxytryptamine's subclass of is recorded as anisole[23].
  • 5-methoxytryptamine's MeSH descriptor ID is recorded as D008735[24].
  • 5-methoxytryptamine's ChEMBL ID is recorded as CHEMBL8165[25].
  • 5-methoxytryptamine's Guide to Pharmacology Ligand ID is recorded as 107[26].
  • 5-methoxytryptamine's Freebase ID is recorded as /m/02q3jxx[27].

Why It Matters

5-methoxytryptamine ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (218 views/month).[2] 5-methoxytryptamine has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] 5-methoxytryptamine is known by 10 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] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  4. [6] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  5. [7] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  6. [8] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  7. [9] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  8. [10] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  9. [11] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  10. [12] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  11. [13] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  12. [14] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  13. [15] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  14. [16] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  15. [17] . Global Substance Registration System. Retrieved . wikidata.org.
  16. [18] . PubChem. Retrieved . wikidata.org.
  17. [19] . PubChem. Retrieved . wikidata.org.
  18. [20] . PubChem. Retrieved . wikidata.org.
  19. [21] . PubChem. Retrieved . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . ChEMBL. Retrieved . wikidata.org.
  24. [26] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  25. [27] . 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). 5-methoxytryptamine. Retrieved May 3, 2026, from https://4ort.xyz/entity/5-methoxytryptamine
MLA “5-methoxytryptamine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/5-methoxytryptamine.
BibTeX @misc{4ortxyz_5-methoxytryptamine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{5-methoxytryptamine}}, year = {2026}, url = {https://4ort.xyz/entity/5-methoxytryptamine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 5-methoxytryptamine — https://4ort.xyz/entity/5-methoxytryptamine (retrieved 2026-05-03)

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