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vindesine

chemical compound
ChemicalSubstance type_of_chemical_entity Q416660
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vindesine

Summary

vindesine is a type of chemical entity[1]. vindesine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (10 views/month).[2]

Key Facts

  • vindesine's instance of is recorded as type of chemical entity[3].
  • vindesine's chemical structure is recorded as Vindesine.svg[4].
  • vindesine's CAS Registry Number is recorded as 53643-48-4[5].
  • vindesine's EC number is recorded as 258-682-2[6].
  • vindesine's canonical SMILES is recorded as CCC1(CC2CC(C3=C(CCN(C2)C1)C4=CC=CC=C4N3)(C5=C(C=C6C(=C5)C78CCN9C7C(C=CC9)(C(C(C8N6C)(C(=O)N)O)O)CC)OC)C(=O)OC)O[7].
  • vindesine's InChI is recorded as InChI=1S/C43H55N5O7/c1-6-39(52)21-25-22-42(38(51)55-5,33-27(13-17-47(23-25)24-39)26-11-8-9-12-30(26)45-33)29-19-28-31(20-32(29)54-4)46(3)35-41(28)15-18-48-16-10-14-40(7-2,34(41)48)36(49)43(35,53)37(44)50/h8-12,14,19-20,25,34-36,45,49,52-53H,6-7,13,15-18,21-24H2,1-5H3,(H2,44,50)/t25-,34+,35-,36-,39+,40-,41-,42+,43+/m1/s1[8].
  • vindesine's InChIKey is recorded as HHJUWIANJFBDHT-KOTLKJBCSA-N[9].
  • vindesine's ATC code is recorded as L01CA03[10].
  • vindesine's chemical formula is recorded as C₄₃H₅₅N₅O₇[11].
  • vindesine's subclass of is recorded as Methyl 13-(10-carbamoyl-12-ethyl-10,11-dihydroxy-5-methoxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraen-4-yl)-17-ethyl-17-hydroxy-1,11-diazatetracyclo[13.3.1.04,12.05,10]nonadeca-4(12),5,7,9-tetraene-13-carboxylate[12].
  • vindesine's has use is recorded as medication[13].
  • vindesine's Commons category is recorded as Vindesine[14].
  • vindesine's MeSH descriptor ID is recorded as D014751[15].
  • vindesine's ChEMBL ID is recorded as CHEMBL219146[16].
  • vindesine's route of administration is recorded as intravenous infusion and defusionههبهلخل[17].
  • vindesine's Freebase ID is recorded as /m/0gdlrj[18].
  • vindesine's UNII is recorded as RSA8KO39WH[19].
  • vindesine's ChemSpider ID is recorded as 37302[20].
  • vindesine's PubChem CID is recorded as 40839[21].
  • vindesine's KEGG ID is recorded as D01769[22].
  • vindesine's MeSH tree code is recorded as D03.132.436.681.827.830[23].
  • vindesine's MeSH tree code is recorded as D03.633.100.473.402.681.827.830[24].
  • vindesine's MeSH tree code is recorded as D03.633.100.496.500.500.681.827.830[25].
  • vindesine's ChEBI ID is recorded as 36373[26].
  • vindesine's DrugBank ID is recorded as DB00309[27].

Why It Matters

vindesine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (10 views/month).[2] vindesine has Wikipedia articles in 13 language editions, a strong signal of global cultural recognition.[28] vindesine is known by 9 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] ↑ . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. 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] ↑ . wikidata.org.
  14. [16] ↑ . ChEMBL. Retrieved . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . Freebase Data Dumps. wikidata.org.
  17. [19] ↑ . DrugBank. Retrieved . wikidata.org.
  18. [20] ↑ . Q2311683. Retrieved . wikidata.org.
  19. [21] ↑ . PubChem. Retrieved . wikidata.org.
  20. [22] ↑ . ChEMBL. Retrieved . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . ChEBI. 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). vindesine. Retrieved May 3, 2026, from https://4ort.xyz/entity/vindesine
MLA “vindesine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/vindesine.
BibTeX @misc{4ortxyz_vindesine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{vindesine}}, year = {2026}, url = {https://4ort.xyz/entity/vindesine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): vindesine — https://4ort.xyz/entity/vindesine (retrieved 2026-05-03)

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