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carnosol

chemical compound
ChemicalSubstance type_of_chemical_entity Q16634054
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carnosol

Summary

carnosol is a type of chemical entity[1]. carnosol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (18 views/month).[2]

Key Facts

  • carnosol's instance of is recorded as type of chemical entity[3].
  • carnosol's chemical structure is recorded as Carnosol.svg[4].
  • carnosol's CAS Registry Number is recorded as 5957-80-2[5].
  • carnosol's canonical SMILES is recorded as CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O[6].
  • carnosol's InChI is recorded as InChI=1S/C20H26O4/c1-10(2)11-8-12-13-9-14-19(3,4)6-5-7-20(14,18(23)24-13)15(12)17(22)16(11)21/h8,10,13-14,21-22H,5-7,9H2,1-4H3/t13-,14-,20+/m0/s1[7].
  • carnosol's InChIKey is recorded as XUSYGBPHQBWGAD-PJSUUKDQSA-N[8].
  • carnosol's chemical formula is recorded as C₂₀H₂₆O₄[9].
  • carnosol's subclass of is recorded as (1R,8S)-3,4-dihydroxy-5-isopropyl-11,11-dimethyl-16-oxatetracyclo[6.6.2.0¹,¹⁰.0²,⁷]hexadeca-2(7),3,5-trien-15-one[10].
  • carnosol's ChEMBL ID is recorded as CHEMBL218693[11].
  • carnosol's Freebase ID is recorded as /m/0j9l4nd[12].
  • carnosol's UNII is recorded as 483O455CKD[13].
  • carnosol's ChemSpider ID is recorded as 390568[14].
  • carnosol's PubChem CID is recorded as 442009[15].
  • carnosol's KEGG ID is recorded as C09069[16].
  • carnosol's ChEBI ID is recorded as 3429[17].
  • carnosol's found in taxon is recorded as Salvia officinalis[18].
  • carnosol's found in taxon is recorded as Salvia mellifera[19].
  • carnosol's found in taxon is recorded as Salvia canariensis[20].
  • carnosol's found in taxon is recorded as Salvia columbariae[21].
  • carnosol's found in taxon is recorded as Salvia munzii[22].
  • carnosol's found in taxon is recorded as Isodon grandifolius[23].
  • carnosol's found in taxon is recorded as 'Salvia africana-lutea' [ L. (1753) ][24].
  • carnosol's found in taxon is recorded as Salvia chionopeplica[25].
  • carnosol's found in taxon is recorded as Salvia przewalskii[26].
  • carnosol's found in taxon is recorded as Hyptis dilatata[27].

Why It Matters

carnosol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (18 views/month).[2] carnosol has Wikipedia articles in 7 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] ↑ . PubChem. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . ChEMBL. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  12. [14] ↑ . Q2311683. Retrieved . wikidata.org.
  13. [15] ↑ . PubChem. Retrieved . wikidata.org.
  14. [16] ↑ . ChEBI. Retrieved . wikidata.org.
  15. [17] ↑ . ChEMBL. Retrieved . wikidata.org.
  16. [18] ↑ . Topical anti-inflammatory activity of Salvia officinalis L. leaves: the relevance of ursolic acid. wikidata.org.
  17. [19] ↑ . C-16 hydroxylated abietane diterpenes from Salvia Mellifera. wikidata.org.
  18. [20] ↑ . Diterpenes from in vitro-grown Salvia canariensis. wikidata.org.
  19. [21] ↑ . Diterpenes from the aerial part of Salvia columbariae. wikidata.org.
  20. [22] ↑ . Abietane diterpenes from Salvia munzii. wikidata.org.
  21. [23] ↑ . Terpenoids from Isodon grandifolia var. Atuntzensis. wikidata.org.
  22. [24] ↑ . Bioactive diterpenes from Orthosiphon labiatus and Salvia africana-lutea. wikidata.org.
  23. [25] ↑ . Abietane diterpenoids from Salvia chinopeplica. wikidata.org.
  24. [26] ↑ . Two new icetexane diterpenoids from Salvia przewalskii. wikidata.org.
  25. [27] ↑ . Tricyclic diterpenes from hyptys dilatata. 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). carnosol. Retrieved May 3, 2026, from https://4ort.xyz/entity/carnosol
MLA “carnosol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/carnosol.
BibTeX @misc{4ortxyz_carnosol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{carnosol}}, year = {2026}, url = {https://4ort.xyz/entity/carnosol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): carnosol — https://4ort.xyz/entity/carnosol (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/carnosol · 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. 19d ago · Shuaib-bot bot · 2026-05-01 view diff on Wikidata ↗
    Subclass of → (1R,8S)-3,4-dihydroxy-5-isopropyl-11,11-dimethyl-16-oxatetracyclo[6.6.2.0¹,¹⁰.0²,⁷]hexadeca-2(7),3,5-trien-15-one
    Found in taxon → Salvia officinalis, Salvia mellifera, Salvia canariensis +22
    Mass → {'unit': 'Q483261', 'amount': '+330.183109'}
    Stereoisomer of → (1S,8R,10R)-3,4-dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one, (1R,8S,10R)-3,4-dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-and-other-short:0||ur */"
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