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vinorelbine

pharmaceutical drug
ChemicalSubstance type_of_chemical_entity Q420532
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vinorelbine

Summary

vinorelbine is a type of chemical entity[1]. vinorelbine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (36 views/month).[2]

Key Facts

  • vinorelbine's instance of is recorded as type of chemical entity[3].
  • vinorelbine's chemical structure is recorded as Vinorelbine2DACS.svg[4].
  • vinorelbine's CAS Registry Number is recorded as 71486-22-1[5].
  • vinorelbine's canonical SMILES is recorded as CCC1=CC2CN(C1)Cc1c([nH]c3ccccc13)C(C(=O)OC)(c1cc3c(cc1OC)N(C)C1C(O)(C(=O)OC)C(OC(C)=O)C4(CC)C=CCN5CCC31C54)C2[6].
  • vinorelbine's InChI is recorded as InChI=1S/C45H54N4O8/c1-8-27-19-28-22-44(40(51)55-6,36-30(25-48(23-27)24-28)29-13-10-11-14-33(29)46-36)32-20-31-34(21-35(32)54-5)47(4)38-43(31)16-18-49-17-12-15-42(9-2,37(43)49)39(57-26(3)50)45(38,53)41(52)56-7/h10-15,19-21,28,37-39,46,53H,8-9,16-18,22-25H2,1-7H3/t28-,37-,38+,39+,42+,43+,44-,45-/m0/s1[7].
  • vinorelbine's InChIKey is recorded as GBABOYUKABKIAF-IELIFDKJSA-N[8].
  • vinorelbine's ATC code is recorded as L01CA04[9].
  • vinorelbine's chemical formula is recorded as C₄₅H₅₄N₄O₈[10].
  • vinorelbine's subclass of is recorded as Vinca alkaloids[11].
  • vinorelbine's has use is recorded as medication[12].
  • vinorelbine's Commons category is recorded as Vinorelbine[13].
  • vinorelbine's MeSH descriptor ID is recorded as D000077235[14].
  • vinorelbine's has part is recorded as nitrogen[15].
  • vinorelbine's has part is recorded as carbon[16].
  • vinorelbine's ChEMBL ID is recorded as CHEMBL3039593[17].
  • vinorelbine's ChEMBL ID is recorded as CHEMBL553025[18].
  • vinorelbine's Guide to Pharmacology Ligand ID is recorded as 7105[19].
  • vinorelbine's Freebase ID is recorded as /m/06_c_x[20].
  • vinorelbine's UNII is recorded as Q6C979R91Y[21].
  • vinorelbine's ChemSpider ID is recorded as 30841604[22].
  • vinorelbine's PubChem CID is recorded as 60780[23].
  • vinorelbine's PubChem CID is recorded as 5311497[24].
  • vinorelbine's KEGG ID is recorded as D08680[25].
  • vinorelbine's MeSH tree code is recorded as D03.132.436.681.827.915[26].
  • vinorelbine's MeSH tree code is recorded as D03.633.100.473.402.681.827.915[27].

Why It Matters

vinorelbine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (36 views/month).[2] vinorelbine has Wikipedia articles in 19 language editions, a strong signal of global cultural recognition.[28] vinorelbine is known by 16 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 . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . ChEBI release 2020-09-01. wikidata.org.
  7. [9] ↑ . DrugBank. wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . NDF-RT. Retrieved . wikidata.org.
  10. [12] ↑ . DrugBank. wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . ChEMBL. Retrieved . wikidata.org.
  16. [18] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  17. [19] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  18. [20] ↑ . Freebase Data Dumps. wikidata.org.
  19. [21] ↑ . NDF-RT. Retrieved . wikidata.org.
  20. [22] ↑ . Q2311683. Retrieved . wikidata.org.
  21. [23] ↑ . PubChem. Retrieved . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . ChEMBL. 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). vinorelbine. Retrieved May 3, 2026, from https://4ort.xyz/entity/vinorelbine
MLA “vinorelbine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/vinorelbine.
BibTeX @misc{4ortxyz_vinorelbine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{vinorelbine}}, year = {2026}, url = {https://4ort.xyz/entity/vinorelbine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): vinorelbine — https://4ort.xyz/entity/vinorelbine (retrieved 2026-05-03)

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