salvinorin A

chemical compound
ChemicalSubstance type_of_chemical_entity Q413512
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salvinorin A

Summary

salvinorin An is a type of chemical entity[1]. It ranks in the top 3% of type_of_chemical_entity entities by monthly Wikipedia readership (509 views/month).[2]

Key Facts

  • salvinorin A's instance of is recorded as type of chemical entity[3].
  • salvinorin A's chemical structure is recorded as Salvinorin A structure.svg[4].
  • salvinorin A's physically interacts with is recorded as opioid receptor kappa 1[5].
  • salvinorin A's CAS Registry Number is recorded as 83729-01-5[6].
  • salvinorin A's EC number is recorded as 689-027-2[7].
  • salvinorin A's canonical SMILES is recorded as CC(=O)OC1CC(C2(CCC3C(=O)OC(CC3(C2C1=O)C)C4=COC=C4)C)C(=O)OC[8].
  • salvinorin A's InChI is recorded as InChI=1S/C23H28O8/c1-12(24)30-16-9-15(20(26)28-4)22(2)7-5-14-21(27)31-17(13-6-8-29-11-13)10-23(14,3)19(22)18(16)25/h6,8,11,14-17,19H,5,7,9-10H2,1-4H3/t14-,15-,16-,17-,19-,22-,23-/m0/s1[9].
  • salvinorin A's InChIKey is recorded as OBSYBRPAKCASQB-AGQYDFLVSA-N[10].
  • salvinorin A's chemical formula is recorded as C₂₃H₂₈O₈[11].
  • salvinorin A's subclass of is recorded as heterocyclic compound[12].
  • salvinorin A's subclass of is recorded as salvinorins[13].
  • salvinorin A's Commons category is recorded as Salvinorin A[14].
  • salvinorin A's MeSH descriptor ID is recorded as C090499[15].
  • salvinorin A's has part is recorded as oxygen[16].
  • salvinorin A's has part is recorded as carbon[17].
  • salvinorin A's ChEMBL ID is recorded as CHEMBL445332[18].
  • salvinorin A's Guide to Pharmacology Ligand ID is recorded as 1666[19].
  • salvinorin A's Freebase ID is recorded as /m/01264l[20].
  • salvinorin A's UNII is recorded as T56W91NG6J[21].
  • salvinorin A's ChemSpider ID is recorded as 113947[22].
  • salvinorin A's PubChem CID is recorded as 128563[23].
  • salvinorin A's ChEBI ID is recorded as 67900[24].
  • salvinorin A's found in taxon is recorded as Salvia divinorum[25].
  • salvinorin A's DrugBank ID is recorded as DB12327[26].
  • salvinorin A's isomeric SMILES is recorded as CC(=O)O[C@H]1CC@HC(=O)OCC@HC(=O)OC">[27].

Why It Matters

salvinorin A ranks in the top 3% of type_of_chemical_entity entities by monthly Wikipedia readership (509 views/month).[2] It has Wikipedia articles in 22 language editions, a strong signal of global cultural recognition.[28] It is known by 14 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] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  4. [6] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  5. [7] . ECHA Substance Infocard database. 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] . wikidata.org.
  13. [15] . Medical Subject Headings. Retrieved . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . ChEMBL. Retrieved . wikidata.org.
  17. [19] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  18. [20] . Freebase Data Dumps. wikidata.org.
  19. [21] . Global Substance Registration System. Retrieved . wikidata.org.
  20. [22] . Q2311683. Retrieved . wikidata.org.
  21. [23] . PubChem. Retrieved . wikidata.org.
  22. [24] . ChEMBL. Retrieved . wikidata.org.
  23. [25] . Salvia divinorum and the unique diterpene hallucinogen, Salvinorin (divinorin) A.. wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . PubChem. Retrieved . 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). salvinorin A. Retrieved May 3, 2026, from https://4ort.xyz/entity/salvinorin-a
MLA “salvinorin A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/salvinorin-a.
BibTeX @misc{4ortxyz_salvinorin-a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{salvinorin A}}, year = {2026}, url = {https://4ort.xyz/entity/salvinorin-a}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): salvinorin A — https://4ort.xyz/entity/salvinorin-a (retrieved 2026-05-03)

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