eburnamenine

chemical compound
ChemicalSubstance type_of_chemical_entity Q15410950
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eburnamenine

Summary

eburnamenine is a type of chemical entity[1]. eburnamenine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (4 views/month).[2]

Key Facts

  • eburnamenine's instance of is recorded as type of chemical entity[3].
  • eburnamenine's canonical SMILES is recorded as CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C=C2[4].
  • eburnamenine's chemical formula is recorded as C₁₉H₂₂N₂[5].
  • eburnamenine is a type of eburna / tacaman alkaloid[6].
  • eburnamenine's Commons category is recorded as Eburnamenine[7].
  • eburnamenine's found in taxon is recorded as Vinca minor[8].
  • eburnamenine's found in taxon is recorded as Hunteria camerunensis[9].
  • eburnamenine's found in taxon is recorded as Hunteria congolana[10].
  • eburnamenine's found in taxon is recorded as Hunteria eburnea[11].
  • eburnamenine's found in taxon is recorded as Hunteria umbellata[12].
  • eburnamenine's found in taxon is recorded as Hunteria zeylanica[13].
  • eburnamenine's found in taxon is recorded as Kopsia hainanensis[14].
  • eburnamenine's found in taxon is recorded as Pleiocarpa mutica[15].
  • eburnamenine's found in taxon is recorded as Kopsia larutensis[16].
  • eburnamenine's found in taxon is recorded as Kopsia arborea[17].
  • eburnamenine's found in taxon is recorded as Kopsia officinalis[18].
  • eburnamenine's found in taxon is recorded as Leuconotis griffithii[19].
  • eburnamenine's found in taxon is recorded as Melodinus khasianus[20].
  • eburnamenine's found in taxon is recorded as Melodinus cochinchinensis[21].
  • eburnamenine's isomeric SMILES is recorded as CC[C@]12CCCN3[C@H]1C4=C(CC3)C5=CC=CC=C5N4C=C2[22].
  • eburnamenine's mass is recorded as {'unit': 'Q483261', 'amount': '+278.178299'}[23].
  • eburnamenine's stereoisomer of is recorded as (-)-Eburnamenine[24].

Why It Matters

eburnamenine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (4 views/month).[2]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . PubChem. Retrieved . wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . Vinca Alkaloids. wikidata.org.
  7. [9] . Alcaloïdes du Comularia camerunensis. wikidata.org.
  8. [10] . Alkaloids of Hunteria zeylanica. wikidata.org.
  9. [11] . The Alkaloids of Hunteria eburnea Pichon. III.1The Tertiary Bases. wikidata.org.
  10. [12] . The Alkaloids of Hunteria eburnea Pichon. III.1The Tertiary Bases. wikidata.org.
  11. [13] . Indole alkaloids from Hunteria zeylanica. wikidata.org.
  12. [14] . Indole Alkaloids fromKopsia hainanensis. wikidata.org.
  13. [15] . Über die Alkaloide vonPleiocarpa muticaBENTH. wikidata.org.
  14. [16] . Absolute configuration of C-16 of eburnane alkaloids from Kopsia larutensis. wikidata.org.
  15. [17] . The isolation and characterization of indole alkaloids from the fruits of Kopsia officinalis. wikidata.org.
  16. [18] . The isolation and characterization of indole alkaloids from the fruits of Kopsia officinalis. wikidata.org.
  17. [19] . Leuconicines A-G and (-)-eburnamaline, biologically active strychnan and eburnan alkaloids from Leuconotis. wikidata.org.
  18. [20] . Melokhanines A-J, Bioactive Monoterpenoid Indole Alkaloids with Diverse Skeletons from Melodinus khasianus. wikidata.org.
  19. [21] . Melokhanines A-J, Bioactive Monoterpenoid Indole Alkaloids with Diverse Skeletons from Melodinus khasianus. wikidata.org.
  20. [22] . PubChem. Retrieved . wikidata.org.
  21. [23] . PubChem. Retrieved . wikidata.org.
  22. [24] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.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). eburnamenine. Retrieved May 3, 2026, from https://4ort.xyz/entity/eburnamenine
MLA “eburnamenine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/eburnamenine.
BibTeX @misc{4ortxyz_eburnamenine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{eburnamenine}}, year = {2026}, url = {https://4ort.xyz/entity/eburnamenine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): eburnamenine — https://4ort.xyz/entity/eburnamenine (retrieved 2026-05-03)

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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. 25d ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Stereoisomer of (-)-Eburnamenine
    Subclass of eburna / tacaman alkaloid
    Aliases
    Subclass of
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
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