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oleanolic acid

chemical compound
ChemicalSubstance type_of_chemical_entity Q418628
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oleanolic acid

Summary

oleanolic acid is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (60 views/month).[2]

Key Facts

  • oleanolic acid's instance of is recorded as type of chemical entity[3].
  • oleanolic acid's chemical structure is recorded as Oleanolic acid.png[4].
  • oleanolic acid's physically interacts with is recorded as G protein-coupled bile acid receptor 1[5].
  • oleanolic acid's GND ID is recorded as 4698695-9[6].
  • oleanolic acid's CAS Registry Number is recorded as 508-02-1[7].
  • oleanolic acid's EC number is recorded as 208-081-6[8].
  • oleanolic acid's canonical SMILES is recorded as CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C[9].
  • oleanolic acid's InChI is recorded as InChI=1S/C30H48O3/c1-25(2)14-16-30(24(32)33)17-15-28(6)19(20(30)18-25)8-9-22-27(5)12-11-23(31)26(3,4)21(27)10-13-29(22,28)7/h8,20-23,31H,9-18H2,1-7H3,(H,32,33)/t20-,21-,22+,23-,27-,28+,29+,30-/m0/s1[10].
  • oleanolic acid's InChIKey is recorded as MIJYXULNPSFWEK-GTOFXWBISA-N[11].
  • oleanolic acid's chemical formula is recorded as C₃₀H₄₈O₃[12].
  • oleanolic acid's subclass of is recorded as carboxylic acid[13].
  • oleanolic acid's subclass of is recorded as (4aS,6aS,6bR,10S,12aR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid[14].
  • oleanolic acid's Commons category is recorded as Oleanolic acid[15].
  • oleanolic acid's MeSH descriptor ID is recorded as D009828[16].
  • oleanolic acid's ChEMBL ID is recorded as CHEMBL168[17].
  • oleanolic acid's Guide to Pharmacology Ligand ID is recorded as 3306[18].
  • oleanolic acid's Freebase ID is recorded as /m/0404cbg[19].
  • oleanolic acid's UNII is recorded as 6SMK8R7TGJ[20].
  • oleanolic acid's ChemSpider ID is recorded as 10062[21].
  • oleanolic acid's PubChem CID is recorded as 10494[22].
  • oleanolic acid's KEGG ID is recorded as C17148[23].
  • oleanolic acid's MeSH tree code is recorded as D02.455.849.919.530.733[24].
  • oleanolic acid's MeSH tree code is recorded as D02.455.849.919.650.600[25].
  • oleanolic acid's ChEBI ID is recorded as 37659[26].
  • oleanolic acid's found in taxon is recorded as Vitex polygama[27].

Why It Matters

oleanolic acid ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (60 views/month).[2] It has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[28] It is known by 34 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] ↑ . wikidata.org.
  5. [7] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  6. [8] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . PubChem. Retrieved . wikidata.org.
  10. [12] ↑ . PubChem. Retrieved . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . ChEMBL. Retrieved . wikidata.org.
  16. [18] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  17. [19] ↑ . Freebase Data Dumps. wikidata.org.
  18. [20] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  19. [21] ↑ . Q2311683. Retrieved . wikidata.org.
  20. [22] ↑ . PubChem. Retrieved . wikidata.org.
  21. [23] ↑ . ChEBI. Retrieved . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . ChEMBL. Retrieved . wikidata.org.
  25. [27] ↑ . Enzymatic inhibitory activity and trypanocidal effects of extracts and compounds from Siphoneugena densiflora O. Berg and Vitex polygama Cham. 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). oleanolic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/oleanolic-acid
MLA “oleanolic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/oleanolic-acid.
BibTeX @misc{4ortxyz_oleanolic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{oleanolic acid}}, year = {2026}, url = {https://4ort.xyz/entity/oleanolic-acid}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): oleanolic acid — https://4ort.xyz/entity/oleanolic-acid (retrieved 2026-05-03)

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