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2-cis,4-trans-xanthoxin

chemical compound
ChemicalSubstance type_of_chemical_entity Q5933737
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2-cis,4-trans-xanthoxin

Summary

2-cis,4-trans-xanthoxin is a type of chemical entity[1]. 2-cis,4-trans-xanthoxin has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • 2-cis,4-trans-xanthoxin's instance of is recorded as type of chemical entity[3].
  • 2-cis,4-trans-xanthoxin's chemical structure is recorded as Xanthoxin.svg[4].
  • 2-cis,4-trans-xanthoxin's CAS Registry Number is recorded as 8066-07-7[5].
  • 2-cis,4-trans-xanthoxin's EC number is recorded as 232-513-2[6].
  • 2-cis,4-trans-xanthoxin's canonical SMILES is recorded as CC(=CC=O)C=CC12C(CC(CC1(O2)C)O)(C)C[7].
  • 2-cis,4-trans-xanthoxin's InChI is recorded as InChI=1S/C15H22O3/c1-11(6-8-16)5-7-15-13(2,3)9-12(17)10-14(15,4)18-15/h5-8,12,17H,9-10H2,1-4H3/b7-5+,11-6-/t12-,14+,15-/m0/s1[8].
  • 2-cis,4-trans-xanthoxin's InChIKey is recorded as ZTALKMXOHWQNIA-TVBSHJCBSA-N[9].
  • 2-cis,4-trans-xanthoxin's chemical formula is recorded as C₁₅H₂₂O₃[10].
  • 2-cis,4-trans-xanthoxin's subclass of is recorded as cyclofarnesoid[11].
  • 2-cis,4-trans-xanthoxin's subclass of is recorded as aldehydes[12].
  • 2-cis,4-trans-xanthoxin's part of is recorded as xanthoxin dehydrogenase activity[13].
  • 2-cis,4-trans-xanthoxin's Freebase ID is recorded as /m/0h1h3cv[14].
  • 2-cis,4-trans-xanthoxin's ChemSpider ID is recorded as 4445403[15].
  • 2-cis,4-trans-xanthoxin's PubChem CID is recorded as 5282222[16].
  • 2-cis,4-trans-xanthoxin's KEGG ID is recorded as C13453[17].
  • 2-cis,4-trans-xanthoxin's ChEBI ID is recorded as 32304[18].
  • 2-cis,4-trans-xanthoxin's found in taxon is recorded as common sunflower[19].
  • 2-cis,4-trans-xanthoxin's found in taxon is recorded as Phaseolus vulgaris[20].
  • 2-cis,4-trans-xanthoxin's found in taxon is recorded as maize[21].
  • 2-cis,4-trans-xanthoxin's found in taxon is recorded as Euphorbia bivonae[22].
  • 2-cis,4-trans-xanthoxin's found in taxon is recorded as tomato[23].
  • 2-cis,4-trans-xanthoxin's found in taxon is recorded as Codium latum[24].
  • 2-cis,4-trans-xanthoxin's isomeric SMILES is recorded as C/C(=C/C=O)/C=C/[C@]12C@(CC@HO)CC@(CC@HO)C">[25].
  • 2-cis,4-trans-xanthoxin's Human Metabolome Database ID is recorded as HMDB0304066[26].
  • 2-cis,4-trans-xanthoxin's KNApSAcK ID is recorded as C00007240[27].

Why It Matters

2-cis,4-trans-xanthoxin has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]

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] ↑ . wikidata.org.
  11. [13] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  12. [14] ↑ . Freebase Data Dumps. wikidata.org.
  13. [15] ↑ . Q2311683. Retrieved . wikidata.org.
  14. [16] ↑ . PubChem. Retrieved . wikidata.org.
  15. [17] ↑ . ChEBI. Retrieved . wikidata.org.
  16. [18] ↑ . ChEBI. Retrieved . wikidata.org.
  17. [19] ↑ . Measurement of xanthoxin in higher plant tissues using 13c labelled internal standards. wikidata.org.
  18. [20] ↑ . Measurement of xanthoxin in higher plant tissues using 13c labelled internal standards. wikidata.org.
  19. [21] ↑ . Measurement of xanthoxin in higher plant tissues using 13c labelled internal standards. wikidata.org.
  20. [22] ↑ . Chemical constituents and antiproliferative activity of Euphorbia bivonae. wikidata.org.
  21. [23] ↑ . Isomeric Ratio and Level of Xanthoxin in Tomato Plants Measured by a New Analytical Method. wikidata.org.
  22. [24] ↑ . Isolation and identification of xanthoxin from marine plants.. wikidata.org.
  23. [25] ↑ . PubChem. Retrieved . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . ChEBI. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . 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). 2-cis,4-trans-xanthoxin. Retrieved May 3, 2026, from https://4ort.xyz/entity/2-cis-4-trans-xanthoxin
MLA “2-cis,4-trans-xanthoxin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/2-cis-4-trans-xanthoxin.
BibTeX @misc{4ortxyz_2-cis-4-trans-xanthoxin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{2-cis,4-trans-xanthoxin}}, year = {2026}, url = {https://4ort.xyz/entity/2-cis-4-trans-xanthoxin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 2-cis,4-trans-xanthoxin — https://4ort.xyz/entity/2-cis-4-trans-xanthoxin (retrieved 2026-05-03)

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