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harmalol

chemical compound
ChemicalSubstance type_of_chemical_entity Q15138221
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harmalol

Summary

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

Key Facts

  • harmalol's instance of is recorded as type of chemical entity[3].
  • harmalol's chemical structure is recorded as Harmalol structure.svg[4].
  • harmalol's CAS Registry Number is recorded as 525-57-5[5].
  • harmalol's EC number is recorded as 208-375-4[6].
  • harmalol's canonical SMILES is recorded as OC=1C=CC2=C(C1)NC=3C(=NCCC23)C[7].
  • harmalol's InChI is recorded as InChI=1S/C12H12N2O/c1-7-12-10(4-5-13-7)9-3-2-8(15)6-11(9)14-12/h2-3,6,14-15H,4-5H2,1H3[8].
  • harmalol's InChIKey is recorded as RHVPEFQDYMMNSY-UHFFFAOYSA-N[9].
  • harmalol's chemical formula is recorded as C₁₂H₁₂N₂O[10].
  • harmalol's subclass of is recorded as beta-carboline alkaloid[11].
  • harmalol's Commons category is recorded as Harmalol[12].
  • harmalol's Freebase ID is recorded as /m/0xnx2vr[13].
  • harmalol's UNII is recorded as 2NQN80556Q[14].
  • harmalol's ChemSpider ID is recorded as 4510170[15].
  • harmalol's PubChem CID is recorded as 3565[16].
  • harmalol's KEGG ID is recorded as C06537[17].
  • harmalol's ChEBI ID is recorded as 27943[18].
  • harmalol's found in taxon is recorded as Peganum harmala[19].
  • harmalol's found in taxon is recorded as Cashew[20].
  • harmalol's found in taxon is recorded as Polygala tenuifolia[21].
  • harmalol's found in taxon is recorded as Passiflora incarnata[22].
  • harmalol's found in taxon is recorded as Tribulus terrestris[23].
  • harmalol's found in taxon is recorded as Banisteriopsis caapi[24].
  • harmalol's found in taxon is recorded as Passiflora amethystina[25].
  • harmalol's found in taxon is recorded as Passiflora citrina[26].
  • harmalol's found in taxon is recorded as Passiflora guatemalensis[27].

Why It Matters

harmalol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (4 views/month).[2] harmalol has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[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] ↑ . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . wikidata.org.
  7. [9] ↑ . ChEBI release 2020-09-01. wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . Q2311683. Retrieved . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . wikidata.org.
  17. [19] ↑ . Chemical and biological investigation of harmal plant. 2. Alkaloidal investigation. wikidata.org.
  18. [20] ↑ . 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.
  19. [21] ↑ . 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.
  20. [22] ↑ . 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.
  21. [23] ↑ . 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.
  22. [24] ↑ . Monoamine oxidase inhibitors in South American hallucinogenic plants: tryptamine and beta-carboline constituents of ayahuasca. 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.

📑 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). harmalol. Retrieved May 3, 2026, from https://4ort.xyz/entity/harmalol
MLA “harmalol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/harmalol.
BibTeX @misc{4ortxyz_harmalol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{harmalol}}, year = {2026}, url = {https://4ort.xyz/entity/harmalol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): harmalol — https://4ort.xyz/entity/harmalol (retrieved 2026-05-03)

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