canagliflozin

chemical compound
ChemicalSubstance type_of_chemical_entity Q5030940
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canagliflozin

Summary

canagliflozin is a type of chemical entity[1]. canagliflozin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (88 views/month).[2]

Key Facts

  • canagliflozin's instance of is recorded as type of chemical entity[3].
  • canagliflozin's chemical structure is recorded as Canagliflozin.svg[4].
  • canagliflozin's chemical structure is recorded as Canagliflozin.png[5].
  • canagliflozin's physically interacts with is recorded as Solute carrier family 5 member 1[6].
  • canagliflozin's physically interacts with is recorded as Solute carrier family 5 member 2[7].
  • canagliflozin's CAS Registry Number is recorded as 842133-18-0[8].
  • canagliflozin's EC number is recorded as 695-192-1[9].
  • canagliflozin's canonical SMILES is recorded as CC1=C(C=C(C=C1)C2C(C(C(C(O2)CO)O)O)O)CC3=CC=C(S3)C4=CC=C(C=C4)F[10].
  • canagliflozin's InChI is recorded as InChI=1S/C24H25FO5S/c1-13-2-3-15(24-23(29)22(28)21(27)19(12-26)30-24)10-16(13)11-18-8-9-20(31-18)14-4-6-17(25)7-5-14/h2-10,19,21-24,26-29H,11-12H2,1H3/t19-,21-,22+,23-,24+/m1/s1[11].
  • canagliflozin's InChIKey is recorded as XTNGUQKDFGDXSJ-ZXGKGEBGSA-N[12].
  • canagliflozin's ATC code is recorded as A10BX11[13].
  • canagliflozin's ATC code is recorded as A10BK02[14].
  • canagliflozin's chemical formula is recorded as C₂₄H₂₅FO₅S[15].
  • canagliflozin's subclass of is recorded as (1xi)-1,5-Anhydro-1-(3-{[5-(4-fluorophenyl)thiophen-2-yl]methyl}-4-methylphenyl)-D-glucitol[16].
  • canagliflozin's has use is recorded as medication[17].
  • canagliflozin's Commons category is recorded as Canagliflozin[18].
  • canagliflozin's MeSH descriptor ID is recorded as D000068896[19].
  • canagliflozin's ChEMBL ID is recorded as CHEMBL2048484[20].
  • canagliflozin's Guide to Pharmacology Ligand ID is recorded as 4582[21].
  • canagliflozin's Freebase ID is recorded as /m/076y2dt[22].
  • canagliflozin's UNII is recorded as 6S49DGR869[23].
  • canagliflozin's ChemSpider ID is recorded as 26333259[24].
  • canagliflozin's PubChem CID is recorded as 24812758[25].
  • canagliflozin's KEGG ID is recorded as D09592[26].
  • canagliflozin's MeSH tree code is recorded as D02.886.778.075[27].

Why It Matters

canagliflozin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (88 views/month).[2] canagliflozin has Wikipedia articles in 13 language editions, a strong signal of global cultural recognition.[28] canagliflozin is known by 6 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] . wikidata.org.
  4. [6] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  5. [7] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  6. [8] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  7. [9] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  8. [10] . PubChem. Retrieved . wikidata.org.
  9. [11] . PubChem. Retrieved . wikidata.org.
  10. [12] . PubChem. Retrieved . wikidata.org.
  11. [13] . DrugBank. wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . PubChem. Retrieved . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . ChEMBL. Retrieved . wikidata.org.
  19. [21] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . Global Substance Registration System. Retrieved . wikidata.org.
  22. [24] . Q2311683. Retrieved . wikidata.org.
  23. [25] . PubChem. Retrieved . wikidata.org.
  24. [26] . ChEMBL. Retrieved . wikidata.org.
  25. [27] . 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). canagliflozin. Retrieved May 3, 2026, from https://4ort.xyz/entity/canagliflozin
MLA “canagliflozin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/canagliflozin.
BibTeX @misc{4ortxyz_canagliflozin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{canagliflozin}}, year = {2026}, url = {https://4ort.xyz/entity/canagliflozin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): canagliflozin — https://4ort.xyz/entity/canagliflozin (retrieved 2026-05-03)

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