vinblastine

chemical compound
ChemicalSubstance group_of_stereoisomers Q282629
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vinblastine

Summary

vinblastine is a group of stereoisomers[1]. vinblastine draws 113 Wikipedia views per month (group_of_stereoisomers category, ranking #131 of 1,063).[2]

Key Facts

  • vinblastine's instance of is recorded as group of stereoisomers[3].
  • vinblastine's chemical structure is recorded as Vinblastine.svg[4].
  • vinblastine's CAS Registry Number is recorded as 865-21-4[5].
  • vinblastine's EC number is recorded as 212-734-0[6].
  • vinblastine'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)OC)O)OC(=O)C)CC)OC)C(=O)OC)O[7].
  • vinblastine's InChI is recorded as InChI=1S/C46H58N4O9/c1-8-42(54)23-28-24-45(40(52)57-6,36-30(15-19-49(25-28)26-42)29-13-10-11-14-33(29)47-36)32-21-31-34(22-35(32)56-5)48(4)38-44(31)17-20-50-18-12-16-43(9-2,37(44)50)39(59-27(3)51)46(38,55)41(53)58-7/h10-14,16,21-22,28,37-39,47,54-55H,8-9,15,17-20,23-26H2,1-7H3/t28-,37+,38-,39-,42+,43-,44-,45+,46+/m1/s1[8].
  • vinblastine's InChIKey is recorded as JXLYSJRDGCGARV-XQKSVPLYSA-N[9].
  • vinblastine's ATC code is recorded as L01CA01[10].
  • vinblastine's chemical formula is recorded as C₄₆H₅₈N₄O₉[11].
  • vinblastine's subclass of is recorded as Vinca alkaloids[12].
  • vinblastine's subclass of is recorded as aspidospermine / aspidofractine / kopsane alkaloid[13].
  • vinblastine's has use is recorded as medication[14].
  • vinblastine's Commons category is recorded as Vinblastine[15].
  • vinblastine's MeSH descriptor ID is recorded as D014747[16].
  • vinblastine's has part is recorded as nitrogen[17].
  • vinblastine's has part is recorded as carbon[18].
  • vinblastine's ChEMBL ID is recorded as CHEMBL22969[19].
  • vinblastine's route of administration is recorded as injection[20].
  • vinblastine's Freebase ID is recorded as /m/07cllr[21].
  • vinblastine's UNII is recorded as 5V9KLZ54CY[22].
  • vinblastine's ChemSpider ID is recorded as 211446[23].
  • vinblastine's PubChem CID is recorded as 241903[24].
  • vinblastine's KEGG ID is recorded as D08675[25].
  • vinblastine's MeSH tree code is recorded as D03.132.436.681.827.650[26].
  • vinblastine's MeSH tree code is recorded as D03.633.100.473.402.681.827.650[27].

Why It Matters

vinblastine draws 113 Wikipedia views per month (group_of_stereoisomers category, ranking #131 of 1,063).[2] vinblastine has Wikipedia articles in 20 language editions, a strong signal of global cultural recognition.[28] vinblastine is known by 7 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] . DrugBank. Retrieved . 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] . NDF-RT. Retrieved . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . DrugBank. wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . ChEMBL. Retrieved . wikidata.org.
  18. [20] . wikidata.org.
  19. [21] . Freebase Data Dumps. wikidata.org.
  20. [22] . DrugBank. Retrieved . wikidata.org.
  21. [23] . Q2311683. Retrieved . wikidata.org.
  22. [24] . PubChem. 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). vinblastine. Retrieved May 3, 2026, from https://4ort.xyz/entity/vinblastine
MLA “vinblastine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/vinblastine.
BibTeX @misc{4ortxyz_vinblastine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{vinblastine}}, year = {2026}, url = {https://4ort.xyz/entity/vinblastine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): vinblastine — https://4ort.xyz/entity/vinblastine (retrieved 2026-05-03)

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