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tocotrienol

chemical compound
ChemicalSubstance group_of_stereoisomers Q27236375
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tocotrienol

Summary

tocotrienol is a group of stereoisomers[1].

Key Facts

  • tocotrienol's instance of is recorded as group of stereoisomers[2].
  • tocotrienol's CAS Registry Number is recorded as 6829-55-6[3].
  • tocotrienol's canonical SMILES is recorded as CC(=CCCC(=CCCC(=CCCC1(CCC2=C(O1)C=CC(=C2)O)C)C)C)C[4].
  • tocotrienol's InChI is recorded as InChI=1S/C26H38O2/c1-20(2)9-6-10-21(3)11-7-12-22(4)13-8-17-26(5)18-16-23-19-24(27)14-15-25(23)28-26/h9,11,13-15,19,27H,6-8,10,12,16-18H2,1-5H3/b21-11+,22-13+[5].
  • tocotrienol's InChIKey is recorded as GJJVAFUKOBZPCB-ZGRPYONQSA-N[6].
  • tocotrienol's chemical formula is recorded as C₂₆H₃₈O₂[7].
  • tocotrienol's subclass of is recorded as chromane[8].
  • tocotrienol's ChEMBL ID is recorded as CHEMBL120643[9].
  • tocotrienol's UNII is recorded as 0867I0N41V[10].
  • tocotrienol's ChemSpider ID is recorded as 8105532[11].
  • tocotrienol's PubChem CID is recorded as 9929901[12].
  • tocotrienol's ChEBI ID is recorded as 197268[13].
  • tocotrienol's found in taxon is recorded as Hippophae rhamnoides[14].
  • tocotrienol's found in taxon is recorded as Iryanthera lancifolia[15].
  • tocotrienol's DrugBank ID is recorded as DB12647[16].
  • tocotrienol's isomeric SMILES is recorded as CC(=CCC/C(=C/CC/C(=C/CCC1(CCC2=C(O1)C=CC(=C2)O)C)/C)/C)C[17].
  • tocotrienol's Human Metabolome Database ID is recorded as HMDB0036368[18].
  • tocotrienol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+382.287'}[19].
  • tocotrienol's SureChEMBL ID is recorded as 1448780[20].
  • tocotrienol's DSSTox substance ID is recorded as DTXSID601336446[21].
  • tocotrienol's UniChem compound ID is recorded as 512037[22].
  • tocotrienol's Probes And Drugs ID is recorded as PD058490[23].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  3. [4] ↑ . PubChem. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . PubChem. Retrieved . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . ChEMBL. Retrieved . wikidata.org.
  9. [10] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  10. [11] ↑ . Q2311683. Retrieved . wikidata.org.
  11. [12] ↑ . PubChem. Retrieved . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . Anti-atherogenic effects of seabuckthorn (Hippophaea rhamnoides) seed oil.. wikidata.org.
  14. [15] ↑ . Butanolides as a common feature of iryanthera lancifolia and virola surinamensis. wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . PubChem. Retrieved . wikidata.org.
  17. [18] ↑ . wikidata.org.
  18. [19] ↑ . PubChem. Retrieved . wikidata.org.
  19. [20] ↑ . wikidata.org.
  20. [21] ↑ . wikidata.org.
  21. [22] ↑ . UniChem. wikidata.org.
  22. [23] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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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). tocotrienol. Retrieved May 3, 2026, from https://4ort.xyz/entity/tocotrienol-q27236375
MLA “tocotrienol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/tocotrienol-q27236375.
BibTeX @misc{4ortxyz_tocotrienol-q27236375_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{tocotrienol}}, year = {2026}, url = {https://4ort.xyz/entity/tocotrienol-q27236375}, note = {Accessed: 2026-05-03}}
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