spiperone

chemical compound
ChemicalSubstance type_of_chemical_entity Q3077150
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spiperone

Summary

spiperone is a type of chemical entity[1]. spiperone ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (40 views/month).[2]

Key Facts

  • spiperone's instance of is recorded as type of chemical entity[3].
  • spiperone's chemical structure is recorded as Spiperone.png[4].
  • spiperone's physically interacts with is recorded as 5-hydroxytryptamine receptor 1A[5].
  • spiperone's physically interacts with is recorded as 5-hydroxytryptamine (serotonin) receptor 1B[6].
  • spiperone's physically interacts with is recorded as 5-hydroxytryptamine receptor 1D[7].
  • spiperone's physically interacts with is recorded as 5-hydroxytryptamine receptor 2A[8].
  • spiperone's physically interacts with is recorded as 5-hydroxytryptamine receptor 2B[9].
  • spiperone's physically interacts with is recorded as 5-hydroxytryptamine receptor 2C[10].
  • spiperone's physically interacts with is recorded as 5-hydroxytryptamine receptor 7[11].
  • spiperone's physically interacts with is recorded as 5-hydroxytryptamine (serotonin) receptor 7[12].
  • spiperone's physically interacts with is recorded as Adrenoceptor alpha 1A[13].
  • spiperone's physically interacts with is recorded as Adrenoceptor alpha 1B[14].
  • spiperone's physically interacts with is recorded as Adrenoceptor alpha 1D[15].
  • spiperone's physically interacts with is recorded as Dopamine receptor D1[16].
  • spiperone's physically interacts with is recorded as Dopamine receptor D3[17].
  • spiperone's physically interacts with is recorded as Dopamine receptor D4[18].
  • spiperone's physically interacts with is recorded as Dopamine receptor D5[19].
  • spiperone's CAS Registry Number is recorded as 749-02-0[20].
  • spiperone's EC number is recorded as 212-024-0[21].
  • spiperone's canonical SMILES is recorded as C1CN(CCC12C(=O)NCN2C3=CC=CC=C3)CCCC(=O)C4=CC=C(C=C4)F[22].
  • spiperone's InChI is recorded as InChI=1S/C23H26FN3O2/c24-19-10-8-18(9-11-19)21(28)7-4-14-26-15-12-23(13-16-26)22(29)25-17-27(23)20-5-2-1-3-6-20/h1-3,5-6,8-11H,4,7,12-17H2,(H,25,29)[23].
  • spiperone's InChIKey is recorded as DKGZKTPJOSAWFA-UHFFFAOYSA-N[24].
  • spiperone's chemical formula is recorded as C₂₃H₂₆FN₃O₂[25].
  • spiperone's subclass of is recorded as butyrophenone[26].
  • spiperone's Commons category is recorded as Spiperone[27].

Why It Matters

spiperone ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (40 views/month).[2] spiperone has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28] spiperone is known by 12 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] . 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] . Global Substance Registration System. 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.
  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). spiperone. Retrieved May 3, 2026, from https://4ort.xyz/entity/spiperone
MLA “spiperone.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/spiperone.
BibTeX @misc{4ortxyz_spiperone_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{spiperone}}, year = {2026}, url = {https://4ort.xyz/entity/spiperone}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): spiperone — https://4ort.xyz/entity/spiperone (retrieved 2026-05-03)

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