(+)-γ-tocopherol

chemical compound
Class type of: DL-γ-tocopherol Q155753

Facts

10 properties
Instance of
type of chemical entity
Subclass of
DL-γ-tocopherol
Part of
tocopherol O-methyltransferase activity, gamma-tocopherol cyclase activity
Canonical SMILES
CC1=C(C=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)O
Chemical formula
C₂₈H₄₈O₂
Isomeric SMILES
CC1=C(C=C2CC[C@@](OC2=C1C)(C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)O
Mass
+416.365
Stereoisomer of
(S)-2,7,8-Trimethyl-2-[(4S,8S)-4,8,12-trimethyltridecyl]-3,4-dihydro-2H-1-benzopyran-6-ol, (2S)-2,7,8-trimethyl-2-[(4S,8R)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-ol
🏷️ Also known as
en Tocopherols en γ-tocopherol en Vitamin E gamma en 2,7,8-trimethyl-2-(4,8,12-trimethyltridecyl)-3,4-dihydro-2H-1-benzopyran-6-ol en 2,7,8-Trimethyl-2-(4,8,12-trimethyltridecyl)-6-chromanol en (2R)-3,4-dihydro-2,7,8-trimethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-2H-1-benzopyran-6-ol en 3,4-Dihydro-2,7,8-trimethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-ol en 7,8-Dimethyltocolo-xylotocopherol en D-gamma-tocopherol en DL-alpha-Tocopherol en gamma-Tocopherol en Methyltocols en O-Xylotocopherol en Tocopherol cs DL-α-tokoferol de DL-alpha-Tocopherol el DL-α-τοκοφερόλη es DL-alfa tocoferol fa گاما-توکوفرول fi DL-alfa-tokoferoli
🔖 Identifiers · 31
CAS Registry Number
54-28-4
Cannabis Database ID
004919
ChEBI ID
18185
ChEMBL ID
CHEMBL2151591
ChemSpider ID
83708
CosIng number
80273
DSSTOX compound identifier
DTXCID0028957
DSSTox substance ID
DTXSID9049031
DrugBank ID
DB15394
E number
E308
EC number
200-201-5
ECHA Substance Infocard ID
100.000.183
Show all 31 identifiers +19
Freebase ID
/m/0466p20
Human Metabolome Database ID
HMDB0001492
KEGG ID
C02483
KNApSAcK ID
C00007365
LIPID MAPS ID
LMPR02020065
MassBank accession ID
MSBNK-Kyoto_Univ-CA000173
MeSH descriptor ID
D024504
Microsoft Academic ID (discontinued)
2781064192
Probes And Drugs ID
PD121899
PubChem CID
92729
Reaxys registry number
93072
SureChEMBL ID
120346
UMLS CUI
C0017054
UniChem compound ID
1067339

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Summary

(+)-γ-tocopherol is a type of chemical entity[1]. (+)-γ-tocopherol is a type of DL-γ-tocopherol[2].

Key Facts

  • Canonical SMILES: CC1=C(C=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)O[3]
  • Chemical formula: C₂₈H₄₈O₂[4]
  • Part of: tocopherol O-methyltransferase activity[5], gamma-tocopherol cyclase activity[6]
  • Found in taxon: Homo sapiens[7], Sesamum indicum[8], soybean[9], Caryodendron orinocense[10], Ginkgo biloba[11], Crataegus monogyna[12], Rubus idaeus[13], Linum usitatissimum[14], Origanum vulgare[15], Origanum dictamnus[16], Origanum onites[17], Satureja thymbra[18], Spinacia oleracea[19], Oryza sativa[20]
  • Isomeric SMILES: CC1=C(C=C2CCC@@(C)CCCC@HCCCC@HCCCC(C)C)OC@@(C)CCCC@HCCCC@HCCCC(C)C)O">[21]
  • Mass: 416.365 dalton[22]
  • Subject has role: antioxidant[23], vitamin[24], primary metabolite[25]

References

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

Direct Wikidata claims

  1. [3] ↑ . PubChem. Retrieved . wikidata.org.
  2. [4] ↑ . PubChem. Retrieved . wikidata.org.
  3. [2] ↑ . wikidata.org.
  4. [5] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  5. [6] ↑ . geneontology.org. Retrieved . geneontology.org. Provenance: wikidata.org.
  6. [7] ↑ . Recon 2.2: from reconstruction to model of human metabolism. wikidata.org.
  7. [8] ↑ . Final Report on the Safety Assessment of Sesame Oil. wikidata.org.
  8. [9] ↑ . Histochemistry. VI. Tocopherols and isoflavones in soybeans (Glycine max MERRILL, seeds).. wikidata.org.
  9. [10] ↑ . Caryodendron orinocense ('nuez de Barinas') oil: tocopherol content and use in cosmetics. wikidata.org.
  10. [11] ↑ . Chemical Composition and Surface Structures of Epicuticular Leaf Waxes of Ginkgo biloba, Magnolia grandiflora and Liriodendron tulipifera. wikidata.org.
  11. [12] ↑ . A comparison of the composition of epicuticular wax from red raspberry (Rubus idaeus L.) and hawthorn (Crataegus monogyna Jacq.) flowers. wikidata.org.
  12. [13] ↑ . A comparison of the composition of epicuticular wax from red raspberry (Rubus idaeus L.) and hawthorn (Crataegus monogyna Jacq.) flowers. wikidata.org.
  13. [14] ↑ . Tocopherols in Flaxseed. wikidata.org.
  14. [15] ↑ . Nutrient antioxidants in oregano. wikidata.org.
  15. [16] ↑ . Nutrient antioxidants in oregano. wikidata.org.
  16. [17] ↑ . Nutrient antioxidants in oregano. wikidata.org.
  17. [18] ↑ . Nutrient antioxidants in oregano. wikidata.org.
  18. [19] ↑ . Determination by HPLC of changes in tocopherol levels in spinach after industrial processing. wikidata.org.
  19. [20] ↑ . Identification and quantitation of γ-oryzanol components and simultaneous assessment of tocols in rice bran oil. wikidata.org.
  20. [21] ↑ . PubChem. Retrieved . wikidata.org.
  21. [22] ↑ . PubChem. Retrieved . wikidata.org.
  22. [23] ↑ . Medical Subject Headings. Retrieved . wikidata.org.
  23. [24] ↑ . Medical Subject Headings. Retrieved . wikidata.org.
  24. [25] ↑ . Reactome. plantreactome.gramene.org. Provenance: 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). (+)-γ-tocopherol. Retrieved November 10, 2026, from https://4ort.xyz/entity/tocopherol-q155753
MLA “(+)-γ-tocopherol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 10 Nov. 2026, https://4ort.xyz/entity/tocopherol-q155753.
BibTeX @misc{4ortxyz_tocopherol-q155753_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(+)-γ-tocopherol}}, year = {2026}, url = {https://4ort.xyz/entity/tocopherol-q155753}, note = {Accessed: 2026-11-10}}
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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. 20w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Stereoisomer of → (S)-2,7,8-Trimethyl-2-[(4S,8S)-4,8,12-trimethyltridecyl]-3,4, (2S)-2,7,8-trimethyl-2-[(4S,8R)-4,8,12-trimethyltridecyl]-3,
    Instance of → type of chemical entity
    Found in taxon → Homo sapiens, Sesamum indicum, soybean +1
    Subclass of → DL-γ-tocopherol
    + 3 other properties edited (see Wikidata diff for full list)
    "Changed [tr] labels, descriptions or aliases: QuickStatements 3.0 batch #37300"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.