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triamcinolone acetonide

chemical compound
ChemicalSubstance type_of_chemical_entity Q2211240
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triamcinolone acetonide

Summary

triamcinolone acetonide is a type of chemical entity[1]. It ranks in the top 3% of type_of_chemical_entity entities by monthly Wikipedia readership (542 views/month).[2]

Key Facts

  • triamcinolone acetonide's instance of is recorded as type of chemical entity[3].
  • triamcinolone acetonide's chemical structure is recorded as Triamcinolone acetonide.svg[4].
  • triamcinolone acetonide's physically interacts with is recorded as Nuclear receptor subfamily 3 group C member 1[5].
  • triamcinolone acetonide's CAS Registry Number is recorded as 76-25-5[6].
  • triamcinolone acetonide's EC number is recorded as 200-948-7[7].
  • triamcinolone acetonide's canonical SMILES is recorded as CC1(OC2CC3C4CCC5=CC(=O)C=CC5(C4(C(CC3(C2(O1)C(=O)CO)C)O)F)C)C[8].
  • triamcinolone acetonide's InChI is recorded as InChI=1S/C24H31FO6/c1-20(2)30-19-10-16-15-6-5-13-9-14(27)7-8-21(13,3)23(15,25)17(28)11-22(16,4)24(19,31-20)18(29)12-26/h7-9,15-17,19,26,28H,5-6,10-12H2,1-4H3/t15-,16-,17-,19+,21-,22-,23-,24+/m0/s1[9].
  • triamcinolone acetonide's InChIKey is recorded as YNDXUCZADRHECN-JNQJZLCISA-N[10].
  • triamcinolone acetonide's chemical formula is recorded as C₂₄H₃₁FO₆[11].
  • triamcinolone acetonide's subclass of is recorded as Kenalog[12].
  • triamcinolone acetonide's Commons category is recorded as Triamcinolone acetonide[13].
  • triamcinolone acetonide's MeSH descriptor ID is recorded as D014222[14].
  • triamcinolone acetonide's ChEMBL ID is recorded as CHEMBL1504[15].
  • triamcinolone acetonide's Guide to Pharmacology Ligand ID is recorded as 2867[16].
  • triamcinolone acetonide's Freebase ID is recorded as /m/03bx74_[17].
  • triamcinolone acetonide's UNII is recorded as F446C597KA[18].
  • triamcinolone acetonide's ChemSpider ID is recorded as 6196[19].
  • triamcinolone acetonide's PubChem CID is recorded as 6436[20].
  • triamcinolone acetonide's KEGG ID is recorded as D00983[21].
  • triamcinolone acetonide's MeSH tree code is recorded as D04.210.500.745.432.915.715[22].
  • triamcinolone acetonide's MeSH tree code is recorded as D04.210.500.908.891.927[23].
  • triamcinolone acetonide's ChEBI ID is recorded as 71418[24].
  • triamcinolone acetonide's DrugBank ID is recorded as DBSALT000860[25].
  • triamcinolone acetonide's Reaxys registry number is recorded as 60069[26].
  • triamcinolone acetonide's isomeric SMILES is recorded as C[C@]12CC@@HOC@@HO">[27].

Why It Matters

triamcinolone acetonide ranks in the top 3% of type_of_chemical_entity entities by monthly Wikipedia readership (542 views/month).[2] It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28] It is known by 10 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] ↑ . 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] ↑ . Freebase Data Dumps. 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] ↑ . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . ChEMBL. Retrieved . wikidata.org.
  23. [25] ↑ . 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). triamcinolone acetonide. Retrieved May 3, 2026, from https://4ort.xyz/entity/triamcinolone-acetonide
MLA “triamcinolone acetonide.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/triamcinolone-acetonide.
BibTeX @misc{4ortxyz_triamcinolone-acetonide_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{triamcinolone acetonide}}, year = {2026}, url = {https://4ort.xyz/entity/triamcinolone-acetonide}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): triamcinolone acetonide — https://4ort.xyz/entity/triamcinolone-acetonide (retrieved 2026-05-03)

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