capecitabine

chemical compound
ChemicalSubstance type_of_chemical_entity Q420207
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capecitabine

Summary

capecitabine is a type of chemical entity[1]. capecitabine ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (104 views/month).[2]

Key Facts

  • capecitabine's instance of is recorded as type of chemical entity[3].
  • capecitabine's chemical structure is recorded as Capecitabine.svg[4].
  • capecitabine's physically interacts with is recorded as Thymidylate synthetase[5].
  • capecitabine's CAS Registry Number is recorded as 154361-50-9[6].
  • capecitabine's EC number is recorded as 604-948-1[7].
  • capecitabine's canonical SMILES is recorded as CCCCCOC(=O)NC1=NC(=O)N(C=C1F)C2C(C(C(O2)C)O)O[8].
  • capecitabine's InChI is recorded as InChI=1S/C15H22FN3O6/c1-3-4-5-6-24-15(23)18-12-9(16)7-19(14(22)17-12)13-11(21)10(20)8(2)25-13/h7-8,10-11,13,20-21H,3-6H2,1-2H3,(H,17,18,22,23)/t8-,10-,11-,13-/m1/s1[9].
  • capecitabine's InChIKey is recorded as GAGWJHPBXLXJQN-UORFTKCHSA-N[10].
  • capecitabine's ATC code is recorded as L01BC06[11].
  • capecitabine's chemical formula is recorded as C₁₅H₂₂FN₃O₆[12].
  • capecitabine's subclass of is recorded as 1-(5-Deoxypentofuranosyl)-5-fluoro-4-{[(pentyloxy)carbonyl]amino}pyrimidin-2(1H)-one[13].
  • capecitabine's has use is recorded as medication[14].
  • capecitabine's Commons category is recorded as Capecitabine[15].
  • capecitabine's MeSH descriptor ID is recorded as D000069287[16].
  • capecitabine's ChEMBL ID is recorded as CHEMBL1773[17].
  • capecitabine's Guide to Pharmacology Ligand ID is recorded as 6799[18].
  • capecitabine's route of administration is recorded as oral administration[19].
  • capecitabine's Freebase ID is recorded as /m/06k8l8[20].
  • capecitabine's UNII is recorded as 6804DJ8Z9U[21].
  • capecitabine's ChemSpider ID is recorded as 54916[22].
  • capecitabine's PubChem CID is recorded as 60953[23].
  • capecitabine's KEGG ID is recorded as C12650[24].
  • capecitabine's KEGG ID is recorded as D01223[25].
  • capecitabine's MeSH tree code is recorded as D03.383.742.680.245.500.425[26].
  • capecitabine's MeSH tree code is recorded as D03.383.742.698.875.404.425[27].

Why It Matters

capecitabine ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (104 views/month).[2] capecitabine has Wikipedia articles in 19 language editions, a strong signal of global cultural recognition.[28] capecitabine is known by 22 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] . ChEMBL. Retrieved . wikidata.org.
  16. [18] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  17. [19] . 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] . 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). capecitabine. Retrieved May 3, 2026, from https://4ort.xyz/entity/capecitabine
MLA “capecitabine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/capecitabine.
BibTeX @misc{4ortxyz_capecitabine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{capecitabine}}, year = {2026}, url = {https://4ort.xyz/entity/capecitabine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): capecitabine — https://4ort.xyz/entity/capecitabine (retrieved 2026-05-03)

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