trilinolein

chemical compound
ChemicalSubstance type_of_chemical_entity Q3539173
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trilinolein

Summary

trilinolein is a type of chemical entity[1]. trilinolein has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • trilinolein's instance of is recorded as type of chemical entity[3].
  • trilinolein's canonical SMILES is recorded as CCCCCC=CCC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCC=CCCCCC)OC(=O)CCCCCCCC=CCC=CCCCCC[4].
  • trilinolein's chemical formula is recorded as C₅₇H₉₈O₆[5].
  • trilinolein is a type of biogenic acyclic ester[6].
  • trilinolein is a type of triglyceride[7].
  • trilinolein is part of omega-hydroxyceramide transacylase activity[8].
  • trilinolein comprises carbon[9].
  • trilinolein comprises oxygen[10].
  • trilinolein comprises hydrogen[11].
  • trilinolein's found in taxon is recorded as Panax ginseng[12].
  • trilinolein's found in taxon is recorded as Panax pseudoginseng[13].
  • trilinolein's found in taxon is recorded as Magnolia sieboldii[14].
  • trilinolein's found in taxon is recorded as Plumbago zeylanica[15].
  • trilinolein's found in taxon is recorded as Barringtonia asiatica[16].
  • trilinolein's found in taxon is recorded as Bauhinia purpurea[17].
  • trilinolein's found in taxon is recorded as Dirca palustris[18].
  • trilinolein's found in taxon is recorded as Inezia integrifolia[19].
  • trilinolein's found in taxon is recorded as Morchella esculenta[20].
  • trilinolein's found in taxon is recorded as Phoradendron reichenbachianum[21].
  • trilinolein's found in taxon is recorded as Sciadopitys verticillata[22].
  • trilinolein's found in taxon is recorded as Panax notoginseng[23].
  • trilinolein's isomeric SMILES is recorded as CCCCC/C=C\C/C=C\CCCCCCCC(=O)OCC(OC(=O)CCCCCCC/C=C\C/C=C\CCCCC)COC(=O)CCCCCCC/C=C\C/C=C\CCCCC[24].
  • trilinolein's mass is recorded as {'unit': 'Q483261', 'amount': '+878.736341'}[25].
  • trilinolein's subject has role is recorded as platelet aggregation inhibitors[26].

Why It Matters

trilinolein has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2] trilinolein is known by 6 alternative names across languages and contexts.[27]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . PubChem. Retrieved . wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . geneontology.org. Retrieved . geneontology.org. Provenance: wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . Determinations of Trilinolein and 1,2– Dilinoleoyl-3-Oleoyl-Glycerol in Various Panax Ginseng by HPLC. wikidata.org.
  11. [13] . Determination of Triacylglycerols in Panax Pseudo-Ginseng by HPLC Polymeric Column. wikidata.org.
  12. [14] . Apoptosis-Inducing costunolide and a novel acyclic monoterpene from the stem bark of Magnolia sieboldii. wikidata.org.
  13. [15] . Cytotoxic constituents from Plumbago zeylanica. wikidata.org.
  14. [16] . New triterpenes from Barringtonia asiatica.. wikidata.org.
  15. [17] . Studies on the Constituents from the Bark ofBauhinia Purpurea. wikidata.org.
  16. [18] . Insecticidal Fatty Acids and Triglycerides from Dirca palustris. wikidata.org.
  17. [19] . Sesquiterpene lactones from Inezia integrifolia. wikidata.org.
  18. [20] . Antioxidant and NF-κB inhibitory constituents isolated fromMorchella esculenta. wikidata.org.
  19. [21] . Cytotoxic activity of moronic acid and identification of the new triterpene 3,4-seco-olean-18-ene-3,28-dioic acid from Phoradendron reichenbachianum. wikidata.org.
  20. [22] . Occurrence of a novel cannabimimetic molecule 2-sciadonoylglycerol (2-eicosa-5',11',14'-trienoylglycerol) in the umbrella pine Sciadopitys verticillata seeds. wikidata.org.
  21. [23] . Chemical Diversity of Panax ginseng, Panax quinquifolium, and Panax notoginseng. wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . PubChem. Retrieved . wikidata.org.
  24. [26] . Medical Subject Headings. Retrieved . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.org.
  2. [27] . 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). trilinolein. Retrieved May 3, 2026, from https://4ort.xyz/entity/trilinolein
MLA “trilinolein.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/trilinolein.
BibTeX @misc{4ortxyz_trilinolein_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{trilinolein}}, year = {2026}, url = {https://4ort.xyz/entity/trilinolein}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): trilinolein — https://4ort.xyz/entity/trilinolein (retrieved 2026-05-03)

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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. 28d ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Has parts
    Instance of type of chemical entity
    Part of
    Subclass of
    + 8 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
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