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aclarubicin

chemical compound
ChemicalSubstance type_of_chemical_entity Q4674302
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aclarubicin

Summary

aclarubicin is a type of chemical entity[1]. aclarubicin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (15 views/month).[2]

Key Facts

  • aclarubicin's instance of is recorded as type of chemical entity[3].
  • aclarubicin's chemical structure is recorded as Aclarubicin.svg[4].
  • aclarubicin's CAS Registry Number is recorded as 57576-44-0[5].
  • aclarubicin's EC number is recorded as 260-824-3[6].
  • aclarubicin's canonical SMILES is recorded as CCC1(CC(C2=C(C1C(=O)OC)C=C3C(=C2O)C(=O)C4=C(C3=O)C=CC=C4O)OC5CC(C(C(O5)C)OC6CC(C(C(O6)C)OC7CCC(=O)C(O7)C)O)N(C)C)O[7].
  • aclarubicin's InChI is recorded as InChI=1S/C42H53NO15/c1-8-42(51)17-28(33-22(35(42)41(50)52-7)14-23-34(38(33)49)37(48)32-21(36(23)47)10-9-11-26(32)45)56-30-15-24(43(5)6)39(19(3)54-30)58-31-16-27(46)40(20(4)55-31)57-29-13-12-25(44)18(2)53-29/h9-11,14,18-20,24,27-31,35,39-40,45-46,49,51H,8,12-13,15-17H2,1-7H3/t18-,19-,20-,24?,27-,28-,29-,30-,31-,35-,39+,40+,42+/m0/s1[8].
  • aclarubicin's InChIKey is recorded as USZYSDMBJDPRIF-SVEJIMAYSA-N[9].
  • aclarubicin's ATC code is recorded as L01DB04[10].
  • aclarubicin's chemical formula is recorded as C₄₂H₅₃NO₁₅[11].
  • aclarubicin's subclass of is recorded as methyl (1R,2R,4S)-4-[(2R,5S,6S)-4-(dimethylamino)-5-[(2S,4S,5S,6S)-4-hydroxy-6-methyl-5-[(2R,6S)-6-methyl-5-oxooxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-2-ethyl-2,5,7-trihydroxy-6,11-dioxo-3,4-dihydro-1H-tetracene-1-carboxylate[12].
  • aclarubicin's has use is recorded as medication[13].
  • aclarubicin's MeSH descriptor ID is recorded as D015250[14].
  • aclarubicin's ChEMBL ID is recorded as CHEMBL1697719[15].
  • aclarubicin's Freebase ID is recorded as /m/04f623y[16].
  • aclarubicin's UNII is recorded as 74KXF8I502[17].
  • aclarubicin's ChemSpider ID is recorded as 1931[18].
  • aclarubicin's PubChem CID is recorded as 42474[19].
  • aclarubicin's PubChem CID is recorded as 451415[20].
  • aclarubicin's PubChem CID is recorded as 86289437[21].
  • aclarubicin's KEGG ID is recorded as D02756[22].
  • aclarubicin's MeSH tree code is recorded as D02.455.426.559.847.562.050.050[23].
  • aclarubicin's MeSH tree code is recorded as D04.615.562.050.050[24].
  • aclarubicin's MeSH tree code is recorded as D09.408.051.059.050[25].
  • aclarubicin's ChEBI ID is recorded as 74619[26].
  • aclarubicin's found in taxon is recorded as Streptomyces galilaeus[27].

Why It Matters

aclarubicin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (15 views/month).[2] aclarubicin has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[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] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. wikidata.org.
  6. [8] ↑ . PubChem. wikidata.org.
  7. [9] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . PubChem. wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  16. [18] ↑ . wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . New anthracycline metabolites from mutant strains of Streptomyces galilaeus MA144-M1. I. Isolation and characterization of various blocked mutants. 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.

📑 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). aclarubicin. Retrieved May 3, 2026, from https://4ort.xyz/entity/aclarubicin
MLA “aclarubicin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/aclarubicin.
BibTeX @misc{4ortxyz_aclarubicin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{aclarubicin}}, year = {2026}, url = {https://4ort.xyz/entity/aclarubicin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): aclarubicin — https://4ort.xyz/entity/aclarubicin (retrieved 2026-05-03)

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