harmine

chemical compound
ChemicalSubstance type_of_chemical_entity Q128381
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harmine

Summary

harmine is a type of chemical entity[1]. harmine ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (434 views/month).[2]

Key Facts

  • harmine's instance of is recorded as type of chemical entity[3].
  • harmine's canonical SMILES is recorded as CC1=NC=CC2=C1NC3=C2C=CC(=C3)OC[4].
  • harmine's chemical formula is recorded as C₁₃H₁₂N₂O[5].
  • harmine is a type of entheogen[6].
  • harmine is a type of beta-carboline alkaloid[7].
  • harmine's Commons category is recorded as Harmine[8].
  • harmine comprises nitrogen[9].
  • harmine comprises carbon[10].
  • harmine's found in taxon is recorded as Peganum harmala[11].
  • harmine's found in taxon is recorded as Peganum nigellastrum[12].
  • harmine's found in taxon is recorded as Cashew[13].
  • harmine's found in taxon is recorded as Passiflora incarnata[14].
  • harmine's found in taxon is recorded as Pinellia ternata[15].
  • harmine's found in taxon is recorded as Simira williamsii[16].
  • harmine's found in taxon is recorded as Acraea andromacha[17].
  • harmine's found in taxon is recorded as Banisteriopsis caapi[18].
  • harmine's found in taxon is recorded as Festuca pratensis[19].
  • harmine's found in taxon is recorded as Grewia bicolor[20].
  • harmine's found in taxon is recorded as Kopsia griffithii[21].
  • harmine's found in taxon is recorded as Oxytropis puberula[22].
  • harmine's found in taxon is recorded as Passiflora actinia[23].
  • harmine's found in taxon is recorded as Passiflora alata[24].
  • harmine's found in taxon is recorded as Passiflora auriculata[25].
  • harmine's found in taxon is recorded as Passiflora boenderi[26].
  • harmine's found in taxon is recorded as Passiflora cincinnata[27].

Why It Matters

harmine ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (434 views/month).[2] harmine has Wikipedia articles in 14 language editions, a strong signal of global cultural recognition.[28] harmine is known by 15 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] . PubChem. Retrieved . wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . Chemical and biological investigation of harmal plant. 2. Alkaloidal investigation. wikidata.org.
  10. [12] . Triterpenoids from Peganum nigellastrum. wikidata.org.
  11. [13] . Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection. wikidata.org.
  12. [14] . Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection. wikidata.org.
  13. [15] . Quantitative analysis of all types of β-carboline alkaloids in medicinal plants and dried edible plants by high performance liquid chromatography with selective fluorometric detection. wikidata.org.
  14. [16] . Inhibiting Activity of Some Glucoindolalkaloids and Iridoids fromSickingia williamsiion Electrically Induced Contractions of Isolated Guinea-pig Ileum. wikidata.org.
  15. [17] . High-performance liquid chromatographic identification of simple β-carboline alkaloids in specimens of heliconiini butterflies. wikidata.org.
  16. [18] . Monoamine oxidase inhibitors in South American hallucinogenic plants: tryptamine and beta-carboline constituents of ayahuasca. wikidata.org.
  17. [19] . Paper chromatography of alkaloids of tall fescue hay. wikidata.org.
  18. [20] . Investigation of Grewia bicolor Juss. wikidata.org.
  19. [21] . Leishmanicidal alkaloids from Kopsia griffithii. wikidata.org.
  20. [22] . Alkaloids of Oxytropis puberula. wikidata.org.
  21. [23] . High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora. wikidata.org.
  22. [24] . High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora. wikidata.org.
  23. [25] . High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora. wikidata.org.
  24. [26] . High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora. wikidata.org.
  25. [27] . High-Speed Extraction and HPLC Fingerprinting of Medicinal Plants – II. Application to Harman Alkaloids of Genus Passiflora. 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). harmine. Retrieved May 3, 2026, from https://4ort.xyz/entity/harmine
MLA “harmine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/harmine.
BibTeX @misc{4ortxyz_harmine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{harmine}}, year = {2026}, url = {https://4ort.xyz/entity/harmine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): harmine — https://4ort.xyz/entity/harmine (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. 16d ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Decomposition point +261
    Subclass of entheogen, beta-carboline alkaloid
    Chemical structure Harmine structure.svg
    Melting point {'unit': 'Q25267', 'amount': '+264'}
    + 1 other property edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
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