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vilanterol

chemical compound
ChemicalSubstance type_of_chemical_entity Q15053666
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vilanterol

Summary

vilanterol is a type of chemical entity[1]. vilanterol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (47 views/month).[2]

Key Facts

  • vilanterol's instance of is recorded as type of chemical entity[3].
  • vilanterol's chemical structure is recorded as Vilanterol.svg[4].
  • vilanterol's physically interacts with is recorded as adrenoceptor beta 2[5].
  • vilanterol's CAS Registry Number is recorded as 503068-34-6[6].
  • vilanterol's EC number is recorded as 690-631-3[7].
  • vilanterol's canonical SMILES is recorded as C1=CC(=C(C(=C1)Cl)COCCOCCCCCCNCC(C2=CC(=C(C=C2)O)CO)O)Cl[8].
  • vilanterol's InChI is recorded as InChI=1S/C24H33Cl2NO5/c25-21-6-5-7-22(26)20(21)17-32-13-12-31-11-4-2-1-3-10-27-15-24(30)18-8-9-23(29)19(14-18)16-28/h5-9,14,24,27-30H,1-4,10-13,15-17H2/t24-/m0/s1[9].
  • vilanterol's InChIKey is recorded as DAFYYTQWSAWIGS-DEOSSOPVSA-N[10].
  • vilanterol's chemical formula is recorded as C₂₄H₃₃Cl₂NO₅[11].
  • vilanterol's subclass of is recorded as 4-(2-((6-(2-((2,6-dichlorobenzyl)oxy)ethoxy)hexyl)aMino)-1-hydroxyethyl)-2-(hydroxyMethyl)phenol[12].
  • vilanterol's has use is recorded as medication[13].
  • vilanterol's Commons category is recorded as Vilanterol[14].
  • vilanterol's ChEMBL ID is recorded as CHEMBL1198857[15].
  • vilanterol's Guide to Pharmacology Ligand ID is recorded as 7353[16].
  • vilanterol's Freebase ID is recorded as /m/0v3h8_y[17].
  • vilanterol's UNII is recorded as 028LZY775B[18].
  • vilanterol's ChemSpider ID is recorded as 8360167[19].
  • vilanterol's PubChem CID is recorded as 10184665[20].
  • vilanterol's KEGG ID is recorded as D09696[21].
  • vilanterol's ChEBI ID is recorded as 75037[22].
  • vilanterol's DrugBank ID is recorded as DB09082[23].
  • vilanterol's significant drug interaction is recorded as sotalol[24].
  • vilanterol's significant drug interaction is recorded as sotalol[25].
  • vilanterol's Reaxys registry number is recorded as 11820500[26].
  • vilanterol's isomeric SMILES is recorded as C1=CC(=C(C(=C1)Cl)COCCOCCCCCCNCC@@HO)ClC@@HO)Cl">[27].

Why It Matters

vilanterol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (47 views/month).[2] vilanterol has Wikipedia articles in 13 language editions, a strong signal of global cultural recognition.[28] vilanterol is known by 5 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 . platform.opentargets.org. Provenance: wikidata.org.
  4. [6] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  5. [7] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . PubChem. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . ChEMBL. Retrieved . wikidata.org.
  14. [16] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  17. [19] ↑ . Q2311683. Retrieved . wikidata.org.
  18. [20] ↑ . PubChem. Retrieved . wikidata.org.
  19. [21] ↑ . ChEBI. Retrieved . wikidata.org.
  20. [22] ↑ . ChEMBL. Retrieved . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . A reference set of clinically relevant adverse drug-drug interactions. wikidata.org.
  23. [25] ↑ . A reference set of clinically relevant adverse drug-drug interactions. wikidata.org.
  24. [26] ↑ . ChEBI. Retrieved . 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.
  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). vilanterol. Retrieved May 3, 2026, from https://4ort.xyz/entity/vilanterol
MLA “vilanterol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/vilanterol.
BibTeX @misc{4ortxyz_vilanterol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{vilanterol}}, year = {2026}, url = {https://4ort.xyz/entity/vilanterol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): vilanterol — https://4ort.xyz/entity/vilanterol (retrieved 2026-05-03)

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