lobelanine

chemical compound
ChemicalSubstance type_of_chemical_entity Q15426225
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lobelanine

Summary

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

Key Facts

  • lobelanine's instance of is recorded as type of chemical entity[3].
  • lobelanine's chemical structure is recorded as Lobelanine.svg[4].
  • lobelanine's CAS Registry Number is recorded as 579-21-5[5].
  • lobelanine's canonical SMILES is recorded as CN1C(CCCC1CC(=O)C2=CC=CC=C2)CC(=O)C3=CC=CC=C3[6].
  • lobelanine's InChI is recorded as InChI=1S/C22H25NO2/c1-23-19(15-21(24)17-9-4-2-5-10-17)13-8-14-20(23)16-22(25)18-11-6-3-7-12-18/h2-7,9-12,19-20H,8,13-16H2,1H3/t19-,20+[7].
  • lobelanine's InChIKey is recorded as IDEMKXUAULKYJV-BGYRXZFFSA-N[8].
  • lobelanine's chemical formula is recorded as C₂₂H₂₅NO₂[9].
  • lobelanine's subclass of is recorded as piperidine alkaloids[10].
  • lobelanine's ChEMBL ID is recorded as CHEMBL331161[11].
  • lobelanine's Freebase ID is recorded as /m/0wzpcsm[12].
  • lobelanine's UNII is recorded as 4XWB84090T[13].
  • lobelanine's ChemSpider ID is recorded as 391009[14].
  • lobelanine's PubChem CID is recorded as 442647[15].
  • lobelanine's KEGG ID is recorded as C10157[16].
  • lobelanine's ChEBI ID is recorded as 6508[17].
  • lobelanine's found in taxon is recorded as Hippobroma longiflora[18].
  • lobelanine's found in taxon is recorded as Cyanea sessilifolia[19].
  • lobelanine's found in taxon is recorded as Lobelia sessilifolia[20].
  • lobelanine's found in taxon is recorded as Lobelia siphilitica[21].
  • lobelanine's found in taxon is recorded as Indian Tobacco[22].
  • lobelanine's isomeric SMILES is recorded as CN1C@HCC(=O)C3=CC=CC=C3C@HCC(=O)C3=CC=CC=C3">[23].
  • lobelanine's KNApSAcK ID is recorded as C00002052[24].
  • lobelanine's mass is recorded as {'unit': 'Q483261', 'amount': '+335.188529'}[25].
  • lobelanine's SureChEMBL ID is recorded as 3448367[26].
  • lobelanine's DSSTox substance ID is recorded as DTXSID10206617[27].

Why It Matters

lobelanine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (1 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] . wikidata.org.
  3. [5] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . PubChem. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . ChEMBL. Retrieved . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . Global Substance Registration System. Retrieved . wikidata.org.
  12. [14] . Q2311683. Retrieved . wikidata.org.
  13. [15] . PubChem. Retrieved . wikidata.org.
  14. [16] . ChEBI. Retrieved . wikidata.org.
  15. [17] . ChEMBL. Retrieved . wikidata.org.
  16. [18] . Piperidine and tetrahydropyridine alkaloids from Lobelia siphilitica and Hippobroma longiflora. wikidata.org.
  17. [19] . Die Konstitution der Lobelia-Alkaloide. wikidata.org.
  18. [20] . Die Konstitution der Lobelia-Alkaloide. wikidata.org.
  19. [21] . Piperidine and tetrahydropyridine alkaloids from Lobelia siphilitica and Hippobroma longiflora. wikidata.org.
  20. [22] . Die Lobelia-Alkaloide. II. wikidata.org.
  21. [23] . PubChem. Retrieved . wikidata.org.
  22. [24] . ChEBI. Retrieved . wikidata.org.
  23. [25] . PubChem. Retrieved . wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard. 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). lobelanine. Retrieved May 3, 2026, from https://4ort.xyz/entity/lobelanine
MLA “lobelanine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/lobelanine.
BibTeX @misc{4ortxyz_lobelanine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{lobelanine}}, year = {2026}, url = {https://4ort.xyz/entity/lobelanine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): lobelanine — https://4ort.xyz/entity/lobelanine (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. 26d ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Subclass of piperidine alkaloids
    Aliases
    Subclass of
    Instance of type of chemical entity
    + 3 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
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