Home › Entities › type_of_chemical_entity › vindoline

vindoline

chemical compound
ChemicalSubstance type_of_chemical_entity Q15427936
Press Enter · cited answer in seconds

vindoline

Summary

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

Key Facts

  • vindoline's instance of is recorded as type of chemical entity[3].
  • vindoline's chemical structure is recorded as Vindoline.svg[4].
  • vindoline's CAS Registry Number is recorded as 2182-14-1[5].
  • vindoline's EC number is recorded as 218-558-0[6].
  • vindoline's canonical SMILES is recorded as CCC12C=CCN3C1C4(CC3)C(C(C2OC(=O)C)(C(=O)OC)O)N(C5=C4C=CC(=C5)OC)C[7].
  • vindoline's InChI is recorded as InChI=1S/C25H32N2O6/c1-6-23-10-7-12-27-13-11-24(19(23)27)17-9-8-16(31-4)14-18(17)26(3)20(24)25(30,22(29)32-5)21(23)33-15(2)28/h7-10,14,19-21,30H,6,11-13H2,1-5H3/t19-,20+,21+,23+,24+,25-/m0/s1[8].
  • vindoline's InChIKey is recorded as CXBGOBGJHGGWIE-ACSXSLCXSA-N[9].
  • vindoline's chemical formula is recorded as C₂₅H₃₂N₂O₆[10].
  • vindoline's subclass of is recorded as vindoline[11].
  • vindoline's part of is recorded as vindoline metabolic process[12].
  • vindoline's part of is recorded as vindoline biosynthetic process[13].
  • vindoline's Commons category is recorded as Vindoline[14].
  • vindoline's ChEMBL ID is recorded as CHEMBL2001832[15].
  • vindoline's Freebase ID is recorded as /m/0xp_dm3[16].
  • vindoline's UNII is recorded as 571PJ1LW03[17].
  • vindoline's ChemSpider ID is recorded as 228680[18].
  • vindoline's PubChem CID is recorded as 260535[19].
  • vindoline's KEGG ID is recorded as C01626[20].
  • vindoline's ChEBI ID is recorded as 16380[21].
  • vindoline's found in taxon is recorded as Catharanthus roseus[22].
  • vindoline's found in taxon is recorded as Catharanthus ovalis[23].
  • vindoline's found in taxon is recorded as Catharanthus trichophyllus[24].
  • vindoline's found in taxon is recorded as Catharanthus pusillus[25].
  • vindoline's found in taxon is recorded as Lonicera morrowii[26].
  • vindoline's isomeric SMILES is recorded as CC[C@@]12C=CCN3[C@@H]1[C@]4(CC3)C@HN(C5=C4C=CC(=C5)OC)CC@HN(C5=C4C=CC(=C5)OC)C">[27].

Why It Matters

vindoline ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (10 views/month).[2] vindoline is known by 6 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] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . Gene Ontology release 2019-11-16. wikidata.org.
  11. [13] ↑ . Gene Ontology release 2019-11-16. wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . ChEMBL. Retrieved . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  16. [18] ↑ . Q2311683. Retrieved . wikidata.org.
  17. [19] ↑ . PubChem. Retrieved . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . ChEBI release 2019-10-02. wikidata.org.
  20. [22] ↑ . Gomaline — A New Indolenine Alkaloid from Catharanthus roseus. wikidata.org.
  21. [23] ↑ . Alcaloïdes mono-indoliques de Catharanthus ovalis. wikidata.org.
  22. [24] ↑ . Catharanthus alkaloids XXXII: isolation of alkaloids from Catharanthus trichophyllus roots and structure elucidation of cathaphylline. wikidata.org.
  23. [25] ↑ . Terpenoid indole alkaloid profile changes in Catharanthus pusillus during development.. wikidata.org.
  24. [26] ↑ . Mechanism for iridane skeleton formation from acyclic monoterpenes in the biosynthesis of secologanin and vindoline in Catharanthus roseus and Lonicera morrowii.. wikidata.org.
  25. [27] ↑ . PubChem. 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). vindoline. Retrieved May 3, 2026, from https://4ort.xyz/entity/vindoline
MLA “vindoline.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/vindoline.
BibTeX @misc{4ortxyz_vindoline_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{vindoline}}, year = {2026}, url = {https://4ort.xyz/entity/vindoline}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): vindoline — https://4ort.xyz/entity/vindoline (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/vindoline · Last refreshed:

Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 24d ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Stereoisomer of → methyl (1R,9S,10S,11R,12R,19R)-11-acetyloxy-12-ethyl-10-hydroxy-5-methoxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5,13-tetraene-10-carboxylate
    Subclass of → vindoline
    Part of → vindoline metabolic process, vindoline biosynthetic process
    Aliases → —
    + 6 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.