fluocinonide

chemical compound
ChemicalSubstance type_of_chemical_entity Q5462791
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fluocinonide

Summary

fluocinonide is a type of chemical entity[1]. fluocinonide ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (172 views/month).[2]

Key Facts

  • fluocinonide's instance of is recorded as type of chemical entity[3].
  • fluocinonide's chemical structure is recorded as Fluocinonide.png[4].
  • fluocinonide's physically interacts with is recorded as Nuclear receptor subfamily 3 group C member 1[5].
  • fluocinonide's CAS Registry Number is recorded as 356-12-7[6].
  • fluocinonide's EC number is recorded as 206-597-6[7].
  • fluocinonide's canonical SMILES is recorded as CC(=O)OCC(=O)C12C(CC3C1(CC(C4(C3CC(C5=CC(=O)C=CC54C)F)F)O)C)OC(O2)(C)C[8].
  • fluocinonide's InChI is recorded as InChI=1S/C26H32F2O7/c1-13(29)33-12-20(32)26-21(34-22(2,3)35-26)10-15-16-9-18(27)17-8-14(30)6-7-23(17,4)25(16,28)19(31)11-24(15,26)5/h6-8,15-16,18-19,21,31H,9-12H2,1-5H3/t15-,16-,18-,19-,21+,23-,24-,25-,26+/m0/s1[9].
  • fluocinonide's InChIKey is recorded as WJOHZNCJWYWUJD-IUGZLZTKSA-N[10].
  • fluocinonide's ATC code is recorded as C05AA11[11].
  • fluocinonide's ATC code is recorded as D07AC08[12].
  • fluocinonide's chemical formula is recorded as C₂₆H₃₂F₂O₇[13].
  • fluocinonide's subclass of is recorded as Lidex[14].
  • fluocinonide's has use is recorded as medication[15].
  • fluocinonide's Commons category is recorded as Fluocinonide[16].
  • fluocinonide's MeSH descriptor ID is recorded as D005447[17].
  • fluocinonide's ChEMBL ID is recorded as CHEMBL1501[18].
  • fluocinonide's Guide to Pharmacology Ligand ID is recorded as 7078[19].
  • fluocinonide's Freebase ID is recorded as /m/07p_b9[20].
  • fluocinonide's UNII is recorded as 2W4A77YPAN[21].
  • fluocinonide's ChemSpider ID is recorded as 9265[22].
  • fluocinonide's PubChem CID is recorded as 9642[23].
  • fluocinonide's KEGG ID is recorded as D00325[24].
  • fluocinonide's MeSH tree code is recorded as D04.210.500.745.432.370.325[25].
  • fluocinonide's MeSH tree code is recorded as D04.210.500.908.394.300[26].
  • fluocinonide's ChEBI ID is recorded as 5109[27].

Why It Matters

fluocinonide ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (172 views/month).[2] fluocinonide has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] fluocinonide 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 . wikidata.org.
  4. [6] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  5. [7] . Global Substance Registration System. 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] . DrugBank. wikidata.org.
  11. [13] . PubChem. Retrieved . 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] . 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] . ChEMBL. Retrieved . wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . ChEBI release 2019-10-02. 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). fluocinonide. Retrieved May 3, 2026, from https://4ort.xyz/entity/fluocinonide
MLA “fluocinonide.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/fluocinonide.
BibTeX @misc{4ortxyz_fluocinonide_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{fluocinonide}}, year = {2026}, url = {https://4ort.xyz/entity/fluocinonide}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): fluocinonide — https://4ort.xyz/entity/fluocinonide (retrieved 2026-05-03)

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