xanomeline

chemical compound
ChemicalSubstance type_of_chemical_entity Q8042940
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xanomeline

Summary

xanomeline is a type of chemical entity[1]. xanomeline ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (104 views/month).[2]

Key Facts

  • xanomeline's instance of is recorded as type of chemical entity[3].
  • xanomeline's chemical structure is recorded as Xanomeline.png[4].
  • xanomeline's physically interacts with is recorded as 5-hydroxytryptamine receptor 1A[5].
  • xanomeline's physically interacts with is recorded as 5-hydroxytryptamine receptor 1B[6].
  • xanomeline's physically interacts with is recorded as 5-hydroxytryptamine receptor 1D[7].
  • xanomeline's physically interacts with is recorded as 5-hydroxytryptamine receptor 1E[8].
  • xanomeline's physically interacts with is recorded as 5-hydroxytryptamine receptor 1F[9].
  • xanomeline's physically interacts with is recorded as 5-hydroxytryptamine receptor 2A[10].
  • xanomeline's physically interacts with is recorded as 5-hydroxytryptamine receptor 2B[11].
  • xanomeline's physically interacts with is recorded as 5-hydroxytryptamine receptor 2C[12].
  • xanomeline's physically interacts with is recorded as 5-hydroxytryptamine receptor 6[13].
  • xanomeline's physically interacts with is recorded as 5-hydroxytryptamine receptor 7[14].
  • xanomeline's physically interacts with is recorded as Cholinergic receptor muscarinic 1[15].
  • xanomeline's physically interacts with is recorded as Cholinergic receptor muscarinic 2[16].
  • xanomeline's physically interacts with is recorded as Cholinergic receptor muscarinic 3[17].
  • xanomeline's physically interacts with is recorded as Cholinergic receptor muscarinic 4[18].
  • xanomeline's physically interacts with is recorded as Cholinergic receptor muscarinic 5[19].
  • xanomeline's CAS Registry Number is recorded as 131986-45-3[20].
  • xanomeline's EC number is recorded as 683-413-4[21].
  • xanomeline's canonical SMILES is recorded as CCCCCCOC1=NSN=C1C2=CCCN(C2)C[22].
  • xanomeline's InChI is recorded as InChI=1S/C14H23N3OS/c1-3-4-5-6-10-18-14-13(15-19-16-14)12-8-7-9-17(2)11-12/h8H,3-7,9-11H2,1-2H3[23].
  • xanomeline's InChIKey is recorded as JOLJIIDDOBNFHW-UHFFFAOYSA-N[24].
  • xanomeline's chemical formula is recorded as C₁₄H₂₃N₃OS[25].
  • xanomeline's subclass of is recorded as chemical compound[26].
  • xanomeline's Commons category is recorded as Xanomeline[27].

Why It Matters

xanomeline ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (104 views/month).[2] xanomeline has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[28]

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] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  15. [17] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  16. [18] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  17. [19] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  18. [20] . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  19. [21] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  20. [22] . PubChem. Retrieved . wikidata.org.
  21. [23] . PubChem. Retrieved . wikidata.org.
  22. [24] . PubChem. Retrieved . wikidata.org.
  23. [25] . PubChem. Retrieved . wikidata.org.
  24. [26] . 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.

📑 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). xanomeline. Retrieved May 3, 2026, from https://4ort.xyz/entity/xanomeline
MLA “xanomeline.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/xanomeline.
BibTeX @misc{4ortxyz_xanomeline_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{xanomeline}}, year = {2026}, url = {https://4ort.xyz/entity/xanomeline}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): xanomeline — https://4ort.xyz/entity/xanomeline (retrieved 2026-05-03)

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