(E)-vulpinic acid

chemical compound
ChemicalSubstance type_of_chemical_entity Q411293
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(E)-vulpinic acid

Summary

(E)-vulpinic acid is a type of chemical entity[1]. (E)-vulpinic acid ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (22 views/month).[2]

Key Facts

  • (E)-vulpinic acid's instance of is recorded as type of chemical entity[3].
  • (E)-vulpinic acid's chemical structure is recorded as Vulpinic acid.svg[4].
  • (E)-vulpinic acid's CAS Registry Number is recorded as 521-52-8[5].
  • (E)-vulpinic acid's EC number is recorded as 208-314-1[6].
  • (E)-vulpinic acid's canonical SMILES is recorded as O=C1OC(C(O)=C1C=2C=CC=CC2)=C(C(=O)OC)C=3C=CC=CC3[7].
  • (E)-vulpinic acid's InChI is recorded as InChI=1S/C19H14O5/c1-23-18(21)15(13-10-6-3-7-11-13)17-16(20)14(19(22)24-17)12-8-4-2-5-9-12/h2-11,20H,1H3/b17-15+[8].
  • (E)-vulpinic acid's InChIKey is recorded as OMZRMXULWNMRAE-BMRADRMJSA-N[9].
  • (E)-vulpinic acid's chemical formula is recorded as C₁₉H₁₄O₅[10].
  • (E)-vulpinic acid's subclass of is recorded as Vulpic acid[11].
  • (E)-vulpinic acid's Commons category is recorded as Vulpinic acid[12].
  • (E)-vulpinic acid's ChEMBL ID is recorded as CHEMBL463212[13].
  • (E)-vulpinic acid's Freebase ID is recorded as /m/04zwf_3[14].
  • (E)-vulpinic acid's UNII is recorded as 13N7RF6M84[15].
  • (E)-vulpinic acid's ChemSpider ID is recorded as 10348869[16].
  • (E)-vulpinic acid's PubChem CID is recorded as 54690323[17].
  • (E)-vulpinic acid's ChEBI ID is recorded as 144250[18].
  • (E)-vulpinic acid's found in taxon is recorded as Tylimanthus tenellus[19].
  • (E)-vulpinic acid's found in taxon is recorded as Pulveroboletus ravenelii[20].
  • (E)-vulpinic acid's found in taxon is recorded as Candelaria concolor[21].
  • (E)-vulpinic acid's found in taxon is recorded as Letharia vulpina[22].
  • (E)-vulpinic acid's found in taxon is recorded as Vulpicida pinastri[23].
  • (E)-vulpinic acid's found in taxon is recorded as Podostictina encoensis[24].
  • (E)-vulpinic acid's found in taxon is recorded as Letharia columbiana[25].
  • (E)-vulpinic acid's isomeric SMILES is recorded as C(\C(OC)=O)(=C/1\C(O)=C(C(=O)O1)C2=CC=CC=C2)/C3=CC=CC=C3[26].
  • (E)-vulpinic acid's KNApSAcK ID is recorded as C00032503[27].

Why It Matters

(E)-vulpinic acid ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (22 views/month).[2] (E)-vulpinic acid has Wikipedia articles in 8 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] . SciFinder. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . PubChem. wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . Freebase Data Dumps. wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . ChEBI release 2021-03-01. wikidata.org.
  17. [19] . New Humulane-Type Sesquiterpenes from the Liverworts Tylimanthus tenellus and Marchantia emarginata subsp. tosana.. wikidata.org.
  18. [20] . Chemical and biological investigation of the fungus Pulveroboletus ravenelii. wikidata.org.
  19. [21] . Chemical constituents of the lichen, Candelaria concolor: a complete NMR and chemical degradative investigation.. wikidata.org.
  20. [22] . Toxicity and antifeedant activity of lichen compounds against the polyphagous herbivorous insect Spodoptera littoralis. wikidata.org.
  21. [23] . QUANTITATIVE VARIATION IN VULPINIC AND PINASTRIC ACIDS PRODUCED BY TUCKERMANNOPSIS PINASTRI (LICHEN-FORMING ASCOMYCOTINA, PARMELIACEAE). wikidata.org.
  22. [24] . STUDIES ON CHILEAN LICHENS XXXI: ADDITIONS TO THE CHEMISTRY OF PSEUDOCYPHELLARIA. wikidata.org.
  23. [25] . 1H and13C-NMR and biological activity investigations of four lichen-derived compounds. wikidata.org.
  24. [26] . 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.

📑 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). (E)-vulpinic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/e-vulpinic-acid
MLA “(E)-vulpinic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/e-vulpinic-acid.
BibTeX @misc{4ortxyz_e-vulpinic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(E)-vulpinic acid}}, year = {2026}, url = {https://4ort.xyz/entity/e-vulpinic-acid}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (E)-vulpinic acid — https://4ort.xyz/entity/e-vulpinic-acid (retrieved 2026-05-03)

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