(+)-γ-tocopherol
chemical compound
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
- Found in taxon
- Homo sapiens, Sesamum indicum, soybean, Caryodendron orinocense, Ginkgo biloba, Crataegus monogyna, Rubus idaeus, Linum usitatissimum, Origanum vulgare, Origanum dictamnus, Origanum onites, Satureja thymbra, Spinacia oleracea, Oryza molida, Hippophae rhamnoides, snap bean, Scutellaria strigillosa, Chlamydomonas reinhardtii, Campanula medium, Hypericum ericoides, Hypericum perfoliatum, Hypericum perforatum, Hypericum tomentosum, Calendula officinalis, Eriocaulon buergerianum, Olea europaea, West African Pepper, Schefflera taiwaniana, Vitex negundo, Vitex negundo var. cannabifolia, Chamaemelum nobile, Arabidopsis thaliana, Brassica oleracea, Brassica rapa, Cucurbita, Phaseolus vulgaris, Perilla frutescens, pomegranate, Prunus avium, tomato, Aronia melanocarpa, Argania spinosa, Trachycarpus fortunei, common sunflower, Vitis vinifera
- 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
- Subject has role
- antioxidant, vitamin, primary metabolite
🏷️ 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
- InChIKey
- QUEDXNHFTDJVIY-DQCZWYHMSA-N
- KEGG ID
- C02483
- KNApSAcK ID
- C00007365
- LIPID MAPS ID
- LMPR02020065
- MassBank accession ID
- MSBNK-Kyoto_Univ-CA000173
- MeSH descriptor ID
- D024504
- MeSH tree code
- D03.383.663.283.909.750.500, D03.633.100.150.909.750.500
- Microsoft Academic ID (discontinued)
- 2781064192
- Probes And Drugs ID
- PD121899
- PubChem CID
- 92729
- Reaxys registry number
- 93072
- SPLASH
- splash10-014i-0000900000-e4ddf53a8c42758f4aae, splash10-0udi-0900100000-bf7aee1c3cc613457a13, splash10-0udi-1900000000-0db174c4f3b12b117164, splash10-0udi-1900000000-261e6db3915086f7e44b, splash10-0udi-1900000000-b372a020231097ff8d00
- SureChEMBL ID
- 120346
- UMLS CUI
- C0017054
- UNII
- 8EF1Z1238F
- UniChem compound ID
- 1067339
🔗 Connections
Found in taxon 44
Subject has role 3
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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]