carnosic acid

chemical compound
ChemicalSubstance type_of_chemical_entity Q412827
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carnosic acid

Summary

carnosic acid is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (42 views/month).[2]

Key Facts

  • carnosic acid's instance of is recorded as type of chemical entity[3].
  • carnosic acid's chemical structure is recorded as Carnosic acid.svg[4].
  • carnosic acid's CAS Registry Number is recorded as 3650-09-7[5].
  • carnosic acid's EC number is recorded as 609-253-7[6].
  • carnosic acid's canonical SMILES is recorded as CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O[7].
  • carnosic acid's InChI is recorded as InChI=1S/C20H28O4/c1-11(2)13-10-12-6-7-14-19(3,4)8-5-9-20(14,18(23)24)15(12)17(22)16(13)21/h10-11,14,21-22H,5-9H2,1-4H3,(H,23,24)/t14-,20+/m0/s1[8].
  • carnosic acid's InChIKey is recorded as QRYRORQUOLYVBU-VBKZILBWSA-N[9].
  • carnosic acid's chemical formula is recorded as C₂₀H₂₈O₄[10].
  • carnosic acid's subclass of is recorded as abietane diterpenoid[11].
  • carnosic acid's MeSH descriptor ID is recorded as C018381[12].
  • carnosic acid's ChEMBL ID is recorded as CHEMBL484853[13].
  • carnosic acid's Freebase ID is recorded as /m/0gg574r[14].
  • carnosic acid's UNII is recorded as LI791SXT24[15].
  • carnosic acid's ChemSpider ID is recorded as 58635[16].
  • carnosic acid's PubChem CID is recorded as 65126[17].
  • carnosic acid's ChEBI ID is recorded as 65585[18].
  • carnosic acid's found in taxon is recorded as Salvia officinalis[19].
  • carnosic acid's found in taxon is recorded as Salvia apiana[20].
  • carnosic acid's found in taxon is recorded as Salvia canariensis[21].
  • carnosic acid's found in taxon is recorded as Lepechinia meyenii[22].
  • carnosic acid's found in taxon is recorded as Lepechinia hastata[23].
  • carnosic acid's found in taxon is recorded as Salvia mellifera[24].
  • carnosic acid's found in taxon is recorded as Salvia columbariae[25].
  • carnosic acid's found in taxon is recorded as Salvia munzii[26].
  • carnosic acid's found in taxon is recorded as Nocardia[27].

Why It Matters

carnosic acid ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (42 views/month).[2] It has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[28] It is known by 5 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] . ChEBI. 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] . Freebase Data Dumps. 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] . ChEBI. Retrieved . wikidata.org.
  17. [19] . Antioxidant Constituents in Sage (Salvia officinalis). wikidata.org.
  18. [20] . 16-hydroxycarnosic acid, a diterpene from Salvia apiana. wikidata.org.
  19. [21] . Diterpenes from in vitro-grown Salvia canariensis. wikidata.org.
  20. [22] . Abietane diterpenoids from Lepechinia meyeni and Lepechinia hastata. wikidata.org.
  21. [23] . Abietane diterpenoids from Lepechinia meyeni and Lepechinia hastata. wikidata.org.
  22. [24] . C-16 hydroxylated abietane diterpenes from Salvia Mellifera. wikidata.org.
  23. [25] . Diterpenes from the aerial part of Salvia columbariae. wikidata.org.
  24. [26] . Abietane diterpenes from Salvia munzii. wikidata.org.
  25. [27] . Oxidation, reduction, and methylation of carnosic acid by Nocardia. 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). carnosic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/carnosic-acid
MLA “carnosic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/carnosic-acid.
BibTeX @misc{4ortxyz_carnosic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{carnosic acid}}, year = {2026}, url = {https://4ort.xyz/entity/carnosic-acid}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): carnosic acid — https://4ort.xyz/entity/carnosic-acid (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/carnosic-acid · 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. 4w ago · KaleemBot bot · 2026-04-30 view diff on Wikidata ↗
    Subclass of abietane diterpenoid
    Found in taxon Salvia officinalis, Salvia apiana, Salvia canariensis +30
    Mass {'unit': 'Q483261', 'amount': '+332.199'}
    Stereoisomer of (4aR,10aR)-5,6-dihydroxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid, salvin, Carnosic acid, Free acid
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ Added [[wikipedia:ur:کارنوسیک ایسڈ]]"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.