dexanabinol

chemical compound
ChemicalSubstance type_of_chemical_entity Q962504
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dexanabinol

Summary

dexanabinol is a type of chemical entity[1]. dexanabinol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (30 views/month).[2]

Key Facts

  • dexanabinol's instance of is recorded as type of chemical entity[3].
  • dexanabinol's chemical structure is recorded as HU-211 structure.png[4].
  • dexanabinol's CAS Registry Number is recorded as 112924-45-5[5].
  • dexanabinol's EC number is recorded as 675-766-8[6].
  • dexanabinol's canonical SMILES is recorded as CCCCCCC(C)(C)C1=CC2=C(C3CC(=CCC3C(O2)(C)C)CO)C(=C1)O[7].
  • dexanabinol's InChI is recorded as InChI=1S/C25H38O3/c1-6-7-8-9-12-24(2,3)18-14-21(27)23-19-13-17(16-26)10-11-20(19)25(4,5)28-22(23)15-18/h10,14-15,19-20,26-27H,6-9,11-13,16H2,1-5H3/t19-,20-/m0/s1[8].
  • dexanabinol's InChIKey is recorded as SSQJFGMEZBFMNV-PMACEKPBSA-N[9].
  • dexanabinol's chemical formula is recorded as C₂₅H₃₈O₃[10].
  • dexanabinol's subclass of is recorded as (10aS)-9-(hydroxymethyl)-6,6-dimethyl-3-(2-methyloctan-2-yl)-6a,7,10,10a-tetrahydrobenzo[c][1]benzopyran-1-ol[11].
  • dexanabinol's MeSH descriptor ID is recorded as C062018[12].
  • dexanabinol's ChEMBL ID is recorded as CHEMBL334533[13].
  • dexanabinol's Freebase ID is recorded as /m/07kj63n[14].
  • dexanabinol's UNII is recorded as R6VT8U5372[15].
  • dexanabinol's ChemSpider ID is recorded as 96934[16].
  • dexanabinol's PubChem CID is recorded as 107778[17].
  • dexanabinol's ChEBI ID is recorded as 230837[18].
  • dexanabinol's DrugBank ID is recorded as DB06444[19].
  • dexanabinol's isomeric SMILES is recorded as CCCCCCC(C)(C)C1=CC2=C([C@H]3CC(=CC[C@@H]3C(O2)(C)C)CO)C(=C1)O[20].
  • dexanabinol's mass is recorded as {'unit': 'Q483261', 'amount': '+386.282'}[21].
  • dexanabinol's ECHA Substance Infocard ID is recorded as 100.201.022[22].
  • dexanabinol's subject has role is recorded as antiarrhythmic agent[23].
  • dexanabinol's subject has role is recorded as excitatory amino acid antagonist[24].
  • dexanabinol's subject has role is recorded as neuroprotective agent[25].
  • dexanabinol's subject has role is recorded as antiemetic[26].
  • dexanabinol's SureChEMBL ID is recorded as 1649687[27].

Why It Matters

dexanabinol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (30 views/month).[2] dexanabinol has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] dexanabinol is known by 4 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] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . ECHA Substance Infocard database. 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] . Medical Subject Headings. Retrieved . wikidata.org.
  11. [13] . ChEMBL. Retrieved . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . Global Substance Registration System. Retrieved . wikidata.org.
  14. [16] . Q2311683. Retrieved . wikidata.org.
  15. [17] . PubChem. Retrieved . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . PubChem. Retrieved . wikidata.org.
  19. [21] . PubChem. Retrieved . wikidata.org.
  20. [22] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  21. [23] . Medical Subject Headings. Retrieved . wikidata.org.
  22. [24] . Medical Subject Headings. Retrieved . wikidata.org.
  23. [25] . Medical Subject Headings. Retrieved . wikidata.org.
  24. [26] . Medical Subject Headings. 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.
  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). dexanabinol. Retrieved May 3, 2026, from https://4ort.xyz/entity/dexanabinol
MLA “dexanabinol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/dexanabinol.
BibTeX @misc{4ortxyz_dexanabinol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{dexanabinol}}, year = {2026}, url = {https://4ort.xyz/entity/dexanabinol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): dexanabinol — https://4ort.xyz/entity/dexanabinol (retrieved 2026-05-03)

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