epirubicin

chemical compound
ChemicalSubstance type_of_chemical_entity Q425122
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epirubicin

Summary

epirubicin is a type of chemical entity[1]. epirubicin has Wikipedia articles in 17 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • epirubicin's instance of is recorded as type of chemical entity[3].
  • epirubicin's canonical SMILES is recorded as CC1C(C(CC(O1)OC2CC(CC3=C(C4=C(C(=C23)O)C(=O)C5=C(C4=O)C=CC=C5OC)O)(C(=O)CO)O)N)O[4].
  • epirubicin's chemical formula is recorded as C₂₇H₂₉NO₁₁[5].
  • epirubicin is a type of anthracycline antibiotic[6].
  • epirubicin is part of response to 4'-epidoxorubicin[7].
  • epirubicin is used for medication[8].
  • epirubicin's Commons category is recorded as Epirubicin[9].
  • epirubicin's found in taxon is recorded as Streptomyces peucetius[10].
  • epirubicin's found in taxon is recorded as Streptomyces venezuelae[11].
  • epirubicin's found in taxon is recorded as Lasiodiplodia theobromae[12].
  • epirubicin's found in taxon is recorded as Streptomyces[13].
  • epirubicin's isomeric SMILES is recorded as C[C@H]1C@@HOC@@HO">[14].
  • epirubicin's mass is recorded as {'unit': 'Q483261', 'amount': '+543.174061'}[15].
  • epirubicin's medical condition treated is recorded as breast cancer[16].
  • epirubicin's medical condition treated is recorded as invasive ductal carcinoma[17].
  • epirubicin's medical condition treated is recorded as gastric adenocarcinoma[18].
  • epirubicin's World Health Organisation international non-proprietary name is recorded as {'lang': 'en', 'text': 'epirubicin'}[19].
  • epirubicin's subject has role is recorded as immunologic adjuvant[20].
  • epirubicin's subject has role is recorded as DNA polymerase inhibitors[21].
  • epirubicin's subject has role is recorded as topoisomerase inhibitor[22].
  • epirubicin's subject has role is recorded as antineoplastic antibiotics[23].
  • epirubicin's subject has role is recorded as topoisomerase II inhibitor[24].
  • epirubicin's stereoisomer of is recorded as 3,5,12-Trihydroxy-3-(hydroxyacetyl)-10-methoxy-6,11-dioxo-1,2,3,4,6,11-hexahydrotetracen-1-yl 3-amino-2,3,6-trideoxyhexopyranoside[25].
  • epirubicin's stereoisomer of is recorded as doxorubicin[26].
  • epirubicin's pregnancy category is recorded as Australian pregnancy category D[27].

Why It Matters

epirubicin has Wikipedia articles in 17 language editions, a strong signal of global cultural recognition.[2] epirubicin is known by 18 alternative names across languages and contexts.[28]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . PubChem. Retrieved . wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . NDF-RT. Retrieved . wikidata.org.
  5. [7] . Gene Ontology release 2019-11-16. wikidata.org.
  6. [8] . DrugBank. wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . Production of the antitumor drug epirubicin (4′-epidoxorubicin) and its precursor by a genetically engineered strain of Streptomyces peucetius. wikidata.org.
  9. [11] . Development of a Streptomyces venezuelae-Based Combinatorial Biosynthetic System for the Production of Glycosylated Derivatives of Doxorubicin and Its Biosynthetic Intermediates. wikidata.org.
  10. [12] . Cytotoxic and Antibacterial Preussomerins from the Mangrove Endophytic Fungus Lasiodiplodia theobromae ZJ-HQ1.. wikidata.org.
  11. [13] . Cytotoxic Anthracycline Metabolites from a Recombinant Streptomyces. wikidata.org.
  12. [14] . PubChem. Retrieved . wikidata.org.
  13. [15] . PubChem. Retrieved . wikidata.org.
  14. [16] . NDF-RT. Retrieved . wikidata.org.
  15. [17] . Drug Indications Extracted from FAERS. Retrieved . wikidata.org.
  16. [18] . Drug Indications Extracted from FAERS. Retrieved . wikidata.org.
  17. [19] . ChEBI. Retrieved . wikidata.org.
  18. [20] . NDF-RT. Retrieved . wikidata.org.
  19. [21] . NDF-RT. Retrieved . wikidata.org.
  20. [22] . NDF-RT. Retrieved . wikidata.org.
  21. [23] . Medical Subject Headings. Retrieved . wikidata.org.
  22. [24] . Medical Subject Headings. Retrieved . wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.org.
  2. [28] . 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). epirubicin. Retrieved May 3, 2026, from https://4ort.xyz/entity/epirubicin
MLA “epirubicin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/epirubicin.
BibTeX @misc{4ortxyz_epirubicin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{epirubicin}}, year = {2026}, url = {https://4ort.xyz/entity/epirubicin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): epirubicin — https://4ort.xyz/entity/epirubicin (retrieved 2026-05-03)

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

Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 28d ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Stereoisomer of 3,5,12-Trihydroxy-3-(hydroxyacetyl)-10-methoxy-6,11-dioxo-1,2,3,4,6,11-hexahydrotetracen-1-yl 3-amino-2,3,6-trideoxyhexopyranoside, doxorubicin
    Instance of type of chemical entity
    Has use medication
    Part of
    + 11 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
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