harman

chemical compound
ChemicalSubstance type_of_chemical_entity Q15411006
Press Enter · cited answer in seconds

harman

Summary

harman is a type of chemical entity[1]. harman ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (48 views/month).[2]

Key Facts

  • harman's instance of is recorded as type of chemical entity[3].
  • harman's chemical structure is recorded as Harmane structure.svg[4].
  • harman's chemical structure is recorded as Harmane.svg[5].
  • harman's CAS Registry Number is recorded as 486-84-0[6].
  • harman's EC number is recorded as 207-642-2[7].
  • harman's canonical SMILES is recorded as CC1=NC=CC2=C1NC3=CC=CC=C23[8].
  • harman's InChI is recorded as InChI=1S/C12H10N2/c1-8-12-10(6-7-13-8)9-4-2-3-5-11(9)14-12/h2-7,14H,1H3[9].
  • harman's InChIKey is recorded as PSFDQSOCUJVVGF-UHFFFAOYSA-N[10].
  • harman's chemical formula is recorded as C₁₂H₁₀N₂[11].
  • harman's subclass of is recorded as beta-carboline alkaloid[12].
  • harman's Commons category is recorded as Harmane[13].
  • harman's MeSH descriptor ID is recorded as C005010[14].
  • harman's ChEMBL ID is recorded as CHEMBL12014[15].
  • harman's Freebase ID is recorded as /m/0xplk15[16].
  • harman's UNII is recorded as 82D6J0535P[17].
  • harman's ChemSpider ID is recorded as 4444755[18].
  • harman's PubChem CID is recorded as 5281404[19].
  • harman's KEGG ID is recorded as C09209[20].
  • harman's ChEBI ID is recorded as 5623[21].
  • harman's found in taxon is recorded as Homo sapiens[22].
  • harman's found in taxon is recorded as Strychnos usambarensis[23].
  • harman's found in taxon is recorded as Prunus dulcis[24].
  • harman's found in taxon is recorded as Cashew[25].
  • harman's found in taxon is recorded as Polygala tenuifolia[26].
  • harman's found in taxon is recorded as Passiflora incarnata[27].

Why It Matters

harman ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (48 views/month).[2] harman has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28] harman is known by 13 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] . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  5. [7] . Global Substance Registration System. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . PubChem. Retrieved . wikidata.org.
  9. [11] . PubChem. Retrieved . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . Medical Subject Headings. Retrieved . 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] . ChEBI. Retrieved . wikidata.org.
  19. [21] . ChEBI. Retrieved . wikidata.org.
  20. [22] . Recon 2.2: from reconstruction to model of human metabolism. wikidata.org.
  21. [23] . Qualitative and quantitative evaluation of bisindole usambarane alkaloids inStrychnos usambarensis roots by high performance liquid chromatography-diode-array. wikidata.org.
  22. [24] . 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.
  23. [25] . 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.
  24. [26] . 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.
  25. [27] . 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.

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). harman. Retrieved May 3, 2026, from https://4ort.xyz/entity/harman
MLA “harman.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/harman.
BibTeX @misc{4ortxyz_harman_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{harman}}, year = {2026}, url = {https://4ort.xyz/entity/harman}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): harman — https://4ort.xyz/entity/harman (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/harman · 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. 27d ago · KaleemBot bot · 2026-05-02 view diff on Wikidata ↗
    Mass {'unit': 'Q483261', 'amount': '+182.084398'}
    Subclass of beta-carboline alkaloid
    Found in taxon Homo sapiens, Strychnos usambarensis, Prunus dulcis +71
    Has characteristic bitterness
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ Added [[wikipedia:ur:ہارمین]]"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.