CHEBI:33270 - α-tocotrienol

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ChEBI Name α-tocotrienol
ChEBI ASCII Name alpha-tocotrienol
Definition A tocotrienol that is chroman-6-ol substituted by methyl groups at positions 2, 5, 7 and 8 and a farnesyl chain at position 2. It has been found in palm oil derived from Elaeis guineensis.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:35062
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Formula C29H44O2
Net Charge 0
Average Mass 424.65846
Monoisotopic Mass 424.33413
InChI InChI=1S/C29H44O2/c1-20(2)12-9-13-21(3)14-10-15-22(4)16-11-18-29(8)19-17-26-25(7)27(30)23(5)24(6)28(26)31-29/h12,14,16,30H,9-11,13,15,17-19H2,1-8H3/b21-14+,22-16+/t29-/m1/s1
SMILES CC(C)=CCC\C(C)=C\CC\C(C)=C\CC[C@]1(C)CCc2c(C)c(O)c(C)c(C)c2O1
Metabolite of Species Details
Homo sapiens (NCBI:txid9606) See: DOI
Roles Classification
Chemical Role(s): antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
(via vitamin E )
(via tocol )
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
fat-soluble vitamin
Vitamins like A, D, E and K that dissolve in fats and are stored in body tissues. Unlike the water-soluble vitamins, these are stored in the body for long periods of time and generally pose a greater risk for toxicity when consumed in excess.
(via vitamin E )
Application(s): neuroprotective agent
Any compound that can be used for the treatment of neurodegenerative disorders.
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ChEBI Ontology
Outgoing α-tocotrienol (CHEBI:33270) has role neuroprotective agent (CHEBI:63726)
α-tocotrienol (CHEBI:33270) has role plant metabolite (CHEBI:76924)
α-tocotrienol (CHEBI:33270) is a tocotrienol (CHEBI:33235)
α-tocotrienol (CHEBI:33270) is a vitamin E (CHEBI:33234)
Synonyms Sources
α-tocotrienol UniProt
α-tocotrienol ChemIDplus
ζ1-tocopherol ChemIDplus
Manual Xrefs Databases
Alpha-Tocotrienol Wikipedia
CPD-15836 MetaCyc
EP2362875 Patent
HMDB0006327 HMDB
US2010105930 Patent
WO2010051277 Patent
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Registry Numbers Types Sources
1721-51-3 CAS Registry Number KEGG COMPOUND
1721-51-3 CAS Registry Number ChemIDplus
45723 Beilstein Registry Number Beilstein
5484296 Beilstein Registry Number Beilstein
5484296 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
16923160 PubMed citation Europe PMC
20823491 PubMed citation Europe PMC
22013739 PubMed citation Europe PMC
22252050 PubMed citation Europe PMC
24013375 PubMed citation Europe PMC
Last Modified
23 October 2015