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valrubicin

pharmaceutical drug
ChemicalSubstance type_of_chemical_entity Q7912593
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valrubicin

Summary

valrubicin is a type of chemical entity[1]. valrubicin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (11 views/month).[2]

Key Facts

  • valrubicin's instance of is recorded as type of chemical entity[3].
  • valrubicin's chemical structure is recorded as Valrubicin.svg[4].
  • valrubicin's CAS Registry Number is recorded as 56124-62-0[5].
  • valrubicin's EC number is recorded as 680-664-1[6].
  • valrubicin's canonical SMILES is recorded as CCCCC(=O)OCC(=O)C1(CC(C2=C(C3=C(C(=C2C1)O)C(=O)C4=C(C3=O)C(=CC=C4)OC)O)OC5CC(C(C(O5)C)O)NC(=O)C(F)(F)F)O[7].
  • valrubicin's InChI is recorded as InChI=1S/C34H36F3NO13/c1-4-5-9-21(40)49-13-20(39)33(47)11-16-24(19(12-33)51-22-10-17(27(41)14(2)50-22)38-32(46)34(35,36)37)31(45)26-25(29(16)43)28(42)15-7-6-8-18(48-3)23(15)30(26)44/h6-8,14,17,19,22,27,41,43,45,47H,4-5,9-13H2,1-3H3,(H,38,46)/t14-,17-,19-,22-,27+,33-/m0/s1[8].
  • valrubicin's InChIKey is recorded as ZOCKGBMQLCSHFP-KQRAQHLDSA-N[9].
  • valrubicin's ATC code is recorded as L01DB09[10].
  • valrubicin's chemical formula is recorded as C₃₄H₃₆F₃NO₁₃[11].
  • valrubicin's subclass of is recorded as 2-Oxo-2-[2,5,12-trihydroxy-7-methoxy-6,11-dioxo-4-({2,3,6-trideoxy-3-[(2,2,2-trifluoro-1-hydroxyethylidene)amino]hexopyranosyl}oxy)-1,2,3,4,6,11-hexahydrotetracen-2-yl]ethyl pentanoate[12].
  • valrubicin's has use is recorded as medication[13].
  • valrubicin's Commons category is recorded as Valrubicin[14].
  • valrubicin's MeSH descriptor ID is recorded as C016163[15].
  • valrubicin's ChEMBL ID is recorded as CHEMBL20225[16].
  • valrubicin's Freebase ID is recorded as /m/07cqhf[17].
  • valrubicin's UNII is recorded as 2C6NUM6878[18].
  • valrubicin's ChemSpider ID is recorded as 38088[19].
  • valrubicin's PubChem CID is recorded as 454216[20].
  • valrubicin's ChEBI ID is recorded as 135876[21].
  • valrubicin's DrugBank ID is recorded as DB00385[22].
  • valrubicin's NCI Thesaurus ID is recorded as C1340[23].
  • valrubicin's isomeric SMILES is recorded as CCCCC(=O)OCC(=O)[C@@]1(O)CC@HC3=C(C1)C(O)=C4C(=O)C5=CC=CC(OC)=C5C(=O)C4=C3OC@HC3=C(C1)C(O)=C4C(=O)C5=CC=CC(OC)=C5C(=O)C4=C3O">[24].
  • valrubicin's HSDB ID is recorded as 7288[25].
  • valrubicin's mass is recorded as {'unit': 'Q483261', 'amount': '+723.213875'}[26].
  • valrubicin's NDF-RT ID is recorded as N0000148597[27].

Why It Matters

valrubicin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (11 views/month).[2] valrubicin is known by 3 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] ↑ . wikidata.org.
  3. [5] ↑ . DrugBank. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  8. [10] ↑ . DrugBank. wikidata.org.
  9. [11] ↑ . PubChem. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . DrugBank. wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . Medical Subject Headings. Retrieved . wikidata.org.
  14. [16] ↑ . ChEMBL. Retrieved . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . NDF-RT. Retrieved . wikidata.org.
  17. [19] ↑ . Q2311683. Retrieved . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . ChEBI release 2019-10-02. wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  22. [24] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  23. [25] ↑ . Hazardous Substances Data Bank. Retrieved . wikidata.org.
  24. [26] ↑ . PubChem. Retrieved . wikidata.org.
  25. [27] ↑ . NDF-RT. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.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). valrubicin. Retrieved May 3, 2026, from https://4ort.xyz/entity/valrubicin
MLA “valrubicin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/valrubicin.
BibTeX @misc{4ortxyz_valrubicin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{valrubicin}}, year = {2026}, url = {https://4ort.xyz/entity/valrubicin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): valrubicin — https://4ort.xyz/entity/valrubicin (retrieved 2026-05-03)

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