Structure via PubChem · Public domain (PubChem)
γ-токоферол
Sign in to saveAlso known as (2R)-3,4-dihydro-2,7,8-trimethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-2H-1-benzopyran-6-ol, D-gamma-tocopherol, 3,4-Dihydro-2,7,8-trimethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-ol, 2,7,8-trimethyl-2-(4,8,12-trimethyltridecyl)-3,4-dihydro-2H-1-benzopyran-6-ol, 2,7,8-Trimethyl-2-(4,8,12-trimethyltridecyl)-6-chromanol, O-Xylotocopherol, 7,8-Dimethyltocolo-xylotocopherol, Vitamin E gamma
химическое соединение, витамин Е
In the Vinony graph
Within Vinony's link graph, γ-токоферол is referenced by 109 other articles, and connects out to chemical compound, vitamin and vitamin C.
It sits within the topics Chembox image size set, ECHA InfoCard ID from Wikidata and E-number additives.
Its subject is documented across 13 Wikipedia language editions.
Chemical data
- Formula
- C28H48O2
- Molecular weight
- 416.7 g/mol
- IUPAC name
- (2R)-2,7,8-trimethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-ol
- SMILES
- CC1=C(C=C2CC[C@@](OC2=C1C)(C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)O
- InChIKey
- QUEDXNHFTDJVIY-DQCZWYHMSA-N
- XLogP
- 10.3
- Polar surface area
- 29.5 Ų
- H-bond donors
- 1
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
- Indications
- inflammation, asthma
via ChEMBL · EBI
Research
3,490 papers- Gamma-tocopherol--an underestimated vitamin?Annals of nutrition & metabolism · 2004
- gamma-tocopherol, the major form of vitamin E in the US diet, deserves more attention.The American journal of clinical nutrition · 2001
- Vitamin E and its anticancer effects.Critical reviews in food science and nutrition · 2019
- The Potential Physiological Role of γ-Tocopherol in Human Health: A Qualitative Review.Nutrition and cancer · 2020
- Engineering of a functional γ-tocopherol transfer protein.Redox biology · 2021
via PubMed
Wikidata facts
- Mass
- 416.365
Show 5 more facts
- found in taxon
- Vitis vinifera
- 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
- canonical SMILES
- CC1=C(C=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)O
- subject has role
- primary metabolite
via Wikidata · CC0