ritanserin

chemical compound
ChemicalSubstance type_of_chemical_entity Q3937260
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ritanserin

Summary

ritanserin is a type of chemical entity[1]. ritanserin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (27 views/month).[2]

Key Facts

  • ritanserin's instance of is recorded as type of chemical entity[3].
  • ritanserin's chemical structure is recorded as Ritanserin2DCSD.svg[4].
  • ritanserin's physically interacts with is recorded as 5-hydroxytryptamine receptor 1A[5].
  • ritanserin's physically interacts with is recorded as 5-hydroxytryptamine receptor 1B[6].
  • ritanserin's physically interacts with is recorded as 5-hydroxytryptamine receptor 1D[7].
  • ritanserin's physically interacts with is recorded as 5-hydroxytryptamine receptor 2A[8].
  • ritanserin's physically interacts with is recorded as 5-hydroxytryptamine receptor 2B[9].
  • ritanserin's physically interacts with is recorded as 5-hydroxytryptamine receptor 2C[10].
  • ritanserin's physically interacts with is recorded as 5-hydroxytryptamine (serotonin) receptor 5A[11].
  • ritanserin's physically interacts with is recorded as 5-hydroxytryptamine receptor 5A[12].
  • ritanserin's physically interacts with is recorded as 5-hydroxytryptamine receptor 6[13].
  • ritanserin's physically interacts with is recorded as 5-hydroxytryptamine receptor 7[14].
  • ritanserin's physically interacts with is recorded as Adrenoceptor alpha 1A[15].
  • ritanserin's physically interacts with is recorded as Adrenoceptor alpha 1B[16].
  • ritanserin's physically interacts with is recorded as Adrenoceptor alpha 1D[17].
  • ritanserin's CAS Registry Number is recorded as 87051-43-2[18].
  • ritanserin's EC number is recorded as 635-929-6[19].
  • ritanserin's canonical SMILES is recorded as CC1=C(C(=O)N2C=CSC2=N1)CCN3CCC(=C(C4=CC=C(C=C4)F)C5=CC=C(C=C5)F)CC3[20].
  • ritanserin's InChI is recorded as InChI=1S/C27H25F2N3OS/c1-18-24(26(33)32-16-17-34-27(32)30-18)12-15-31-13-10-21(11-14-31)25(19-2-6-22(28)7-3-19)20-4-8-23(29)9-5-20/h2-9,16-17H,10-15H2,1H3[21].
  • ritanserin's InChIKey is recorded as JUQLTPCYUFPYKE-UHFFFAOYSA-N[22].
  • ritanserin's chemical formula is recorded as C₂₇H₂₅F₂N₃OS[23].
  • ritanserin's subclass of is recorded as chemical compound[24].
  • ritanserin's Commons category is recorded as Ritanserin[25].
  • ritanserin's MeSH descriptor ID is recorded as D016713[26].
  • ritanserin's ChEMBL ID is recorded as CHEMBL267777[27].

Why It Matters

ritanserin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (27 views/month).[2] ritanserin is known by 5 alternative names across languages and contexts.[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] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  17. [19] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  18. [20] . PubChem. Retrieved . wikidata.org.
  19. [21] . PubChem. Retrieved . wikidata.org.
  20. [22] . PubChem. Retrieved . wikidata.org.
  21. [23] . PubChem. Retrieved . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . ChEMBL. Retrieved . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . 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). ritanserin. Retrieved May 3, 2026, from https://4ort.xyz/entity/ritanserin
MLA “ritanserin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/ritanserin.
BibTeX @misc{4ortxyz_ritanserin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{ritanserin}}, year = {2026}, url = {https://4ort.xyz/entity/ritanserin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): ritanserin — https://4ort.xyz/entity/ritanserin (retrieved 2026-05-03)

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