tetrahydroisoquinoline

chemical compound
ChemicalSubstance type_of_chemical_entity Q411677
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tetrahydroisoquinoline

Summary

tetrahydroisoquinoline is a type of chemical entity[1]. tetrahydroisoquinoline ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (46 views/month).[2]

Key Facts

  • tetrahydroisoquinoline's instance of is recorded as type of chemical entity[3].
  • tetrahydroisoquinoline's chemical structure is recorded as Tetrahydroisoquinoline-structure.svg[4].
  • tetrahydroisoquinoline's CAS Registry Number is recorded as 91-21-4[5].
  • tetrahydroisoquinoline's EC number is recorded as 202-050-0[6].
  • tetrahydroisoquinoline's canonical SMILES is recorded as C1CNCC2=CC=CC=C21[7].
  • tetrahydroisoquinoline's InChI is recorded as InChI=1S/C9H11N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-4,10H,5-7H2[8].
  • tetrahydroisoquinoline's InChIKey is recorded as UWYZHKAOTLEWKK-UHFFFAOYSA-N[9].
  • tetrahydroisoquinoline's chemical formula is recorded as C₉H₁₁N[10].
  • tetrahydroisoquinoline's subclass of is recorded as isoquinoline alkaloid[11].
  • tetrahydroisoquinoline's Commons category is recorded as Tetrahydroisoquinoline[12].
  • tetrahydroisoquinoline's ChEMBL ID is recorded as CHEMBL14346[13].
  • tetrahydroisoquinoline's PDB structure ID is recorded as 4MRF[14].
  • tetrahydroisoquinoline's Freebase ID is recorded as /m/03cwxtv[15].
  • tetrahydroisoquinoline's UNII is recorded as 56W89FBX3E[16].
  • tetrahydroisoquinoline's RTECS number is recorded as NX4900000[17].
  • tetrahydroisoquinoline's ChemSpider ID is recorded as 6779[18].
  • tetrahydroisoquinoline's PubChem CID is recorded as 7046[19].
  • tetrahydroisoquinoline's ChEBI ID is recorded as 125498[20].
  • tetrahydroisoquinoline's found in taxon is recorded as Nelumbo nucifera[21].
  • tetrahydroisoquinoline's topic's main category is recorded as Category:Tetrahydroisoquinoline[22].
  • tetrahydroisoquinoline's Human Metabolome Database ID is recorded as HMDB0012489[23].
  • tetrahydroisoquinoline's mass is recorded as {'unit': 'Q483261', 'amount': '+133.089'}[24].
  • tetrahydroisoquinoline's melting point is recorded as {'unit': 'Q25267', 'amount': '-30.0'}[25].
  • tetrahydroisoquinoline's ECHA Substance Infocard ID is recorded as 100.001.864[26].
  • tetrahydroisoquinoline's NSC number is recorded as 15312[27].

Why It Matters

tetrahydroisoquinoline ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (46 views/month).[2] tetrahydroisoquinoline has Wikipedia articles in 6 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] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . Global Substance Registration System. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . PubChem. Retrieved . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . ChEMBL. Retrieved . wikidata.org.
  12. [14] . Protein Data Bank. Retrieved . wikidata.org.
  13. [15] . Freebase Data Dumps. wikidata.org.
  14. [16] . Global Substance Registration System. Retrieved . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . Q2311683. Retrieved . wikidata.org.
  17. [19] . PubChem. Retrieved . wikidata.org.
  18. [20] . ChEBI. Retrieved . wikidata.org.
  19. [21] . Alkaloid constituents from flower buds and leaves of sacred lotus (Nelumbo nucifera, Nymphaeaceae) with melanogenesis inhibitory activity in B16 melanoma cells.. wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . PubChem. Retrieved . wikidata.org.
  23. [25] . Jean-Claude Bradley Open Melting Point Dataset. wikidata.org.
  24. [26] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  25. [27] . 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). tetrahydroisoquinoline. Retrieved May 3, 2026, from https://4ort.xyz/entity/tetrahydroisoquinoline
MLA “tetrahydroisoquinoline.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/tetrahydroisoquinoline.
BibTeX @misc{4ortxyz_tetrahydroisoquinoline_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{tetrahydroisoquinoline}}, year = {2026}, url = {https://4ort.xyz/entity/tetrahydroisoquinoline}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): tetrahydroisoquinoline — https://4ort.xyz/entity/tetrahydroisoquinoline (retrieved 2026-05-03)

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