fexofenadine

Antihistamine medication
ChemicalSubstance group_of_stereoisomers Q415122
Press Enter · cited answer in seconds

fexofenadine

Summary

fexofenadine is a group of stereoisomers[1]. fexofenadine ranks in the top 1% of group_of_stereoisomers entities by monthly Wikipedia readership (2,224 views/month).[2]

Key Facts

  • fexofenadine's instance of is recorded as group of stereoisomers[3].
  • fexofenadine's chemical structure is recorded as Fexofenadine2DCSD.svg[4].
  • fexofenadine's physically interacts with is recorded as Histamine receptor H1[5].
  • fexofenadine's CAS Registry Number is recorded as 83799-24-0[6].
  • fexofenadine's EC number is recorded as 801-893-7[7].
  • fexofenadine's canonical SMILES is recorded as CC(C)(C1=CC=C(C=C1)C(CCCN2CCC(CC2)C(C3=CC=CC=C3)(C4=CC=CC=C4)O)O)C(=O)O[8].
  • fexofenadine's InChI is recorded as InChI=1S/C32H39NO4/c1-31(2,30(35)36)25-17-15-24(16-18-25)29(34)14-9-21-33-22-19-28(20-23-33)32(37,26-10-5-3-6-11-26)27-12-7-4-8-13-27/h3-8,10-13,15-18,28-29,34,37H,9,14,19-23H2,1-2H3,(H,35,36)[9].
  • fexofenadine's InChIKey is recorded as RWTNPBWLLIMQHL-UHFFFAOYSA-N[10].
  • fexofenadine's ATC code is recorded as R06AX26[11].
  • fexofenadine's chemical formula is recorded as C₃₂H₃₉NO₄[12].
  • fexofenadine's subclass of is recorded as piperidine alkaloids[13].
  • fexofenadine's subclass of is recorded as carboxylic acid[14].
  • fexofenadine's has use is recorded as medication[15].
  • fexofenadine's Commons category is recorded as Fexofenadine[16].
  • fexofenadine's MeSH descriptor ID is recorded as C093230[17].
  • fexofenadine's ChEMBL ID is recorded as CHEMBL914[18].
  • fexofenadine's Guide to Pharmacology Ligand ID is recorded as 4819[19].
  • fexofenadine's Freebase ID is recorded as /m/03vtmt[20].
  • fexofenadine's UNII is recorded as E6582LOH6V[21].
  • fexofenadine's ChemSpider ID is recorded as 3231[22].
  • fexofenadine's PubChem CID is recorded as 3348[23].
  • fexofenadine's KEGG ID is recorded as C06999[24].
  • fexofenadine's KEGG ID is recorded as D07958[25].
  • fexofenadine's ChEBI ID is recorded as 5050[26].
  • fexofenadine's found in taxon is recorded as Streptomyces platensis[27].

Why It Matters

fexofenadine ranks in the top 1% of group_of_stereoisomers entities by monthly Wikipedia readership (2,224 views/month).[2] fexofenadine has Wikipedia articles in 21 language editions, a strong signal of global cultural recognition.[28] fexofenadine is known by 9 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] . 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] . DrugBank. wikidata.org.
  10. [12] . PubChem. Retrieved . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . ChEMBL. Retrieved . wikidata.org.
  17. [19] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  18. [20] . Freebase Data Dumps. wikidata.org.
  19. [21] . Global Substance Registration System. Retrieved . wikidata.org.
  20. [22] . Q2311683. Retrieved . wikidata.org.
  21. [23] . PubChem. Retrieved . wikidata.org.
  22. [24] . ChEBI. Retrieved . wikidata.org.
  23. [25] . ChEBI. Retrieved . wikidata.org.
  24. [26] . ChEMBL. Retrieved . wikidata.org.
  25. [27] . A new cytochrome P450 belonging to the 107L subfamily is responsible for the efficient hydroxylation of the drug terfenadine by Streptomyces platensis. 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). fexofenadine. Retrieved May 3, 2026, from https://4ort.xyz/entity/fexofenadine
MLA “fexofenadine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/fexofenadine.
BibTeX @misc{4ortxyz_fexofenadine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{fexofenadine}}, year = {2026}, url = {https://4ort.xyz/entity/fexofenadine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): fexofenadine — https://4ort.xyz/entity/fexofenadine (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/fexofenadine · Last refreshed: