CHEBI:45713 - trans-resveratrol

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ChEBI Name trans-resveratrol
ChEBI ASCII Name trans-resveratrol
Definition A resveratrol in which the double bond has E configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:36000, CHEBI:45712
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Formula C14H12O3
Net Charge 0
Average Mass 228.24328
Monoisotopic Mass 228.07864
InChI InChI=1S/C14H12O3/c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11/h1-9,15-17H/b2-1+
SMILES Oc1ccc(cc1)\C=C\c1cc(O)cc(O)c1
Metabolite of Species Details
Vitis vinifera (NCBI:txid29760) See: PubMed
Arachis hypogaea (NCBI:txid3818) Found in seed (BTO:0001226). See: PubMed
Roles Classification
Chemical Role(s): antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
(via resveratrol )
radical scavenger
A role played by a substance that can react readily with, and thereby eliminate, radicals.
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.
A toxin made by a plant that acts against an organism attacking it.
(via resveratrol )
quorum sensing inhibitor
Any compound that interferes with bacterial communication (quorum sensing, QS).
glioma-associated oncogene inhibitor
An inhibitor of any of the glioma-associated oncogene (GLI) proteins.
(via resveratrol )
Application(s): geroprotector
Any compound that supports healthy aging, slows the biological aging process, or extends lifespan.
(via resveratrol )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing trans-resveratrol (CHEBI:45713) has role antioxidant (CHEBI:22586)
trans-resveratrol (CHEBI:45713) has role phytoalexin (CHEBI:26115)
trans-resveratrol (CHEBI:45713) has role plant metabolite (CHEBI:76924)
trans-resveratrol (CHEBI:45713) has role quorum sensing inhibitor (CHEBI:138977)
trans-resveratrol (CHEBI:45713) has role radical scavenger (CHEBI:48578)
trans-resveratrol (CHEBI:45713) is a resveratrol (CHEBI:27881)
Incoming (−)-trans-ε-viniferin (CHEBI:10556) has functional parent trans-resveratrol (CHEBI:45713)
(+)-trans-ε-viniferin (CHEBI:76137) has functional parent trans-resveratrol (CHEBI:45713)
(2R,3R)-trans-δ-viniferin (CHEBI:76147) has functional parent trans-resveratrol (CHEBI:45713)
(2R,3S)-trans-ε-viniferin (CHEBI:76143) has functional parent trans-resveratrol (CHEBI:45713)
(2S,3R)-trans-ε-viniferin (CHEBI:76140) has functional parent trans-resveratrol (CHEBI:45713)
(2S,3S)-trans-δ-viniferin (CHEBI:76141) has functional parent trans-resveratrol (CHEBI:45713)
(E)-trans-miyabenol C (CHEBI:76193) has functional parent trans-resveratrol (CHEBI:45713)
3-methoxy-4',5-dihydroxy-trans-stilbene (CHEBI:63672) has functional parent trans-resveratrol (CHEBI:45713)
trans-diptoindonesin B (CHEBI:76196) has functional parent trans-resveratrol (CHEBI:45713)
trans-piceid (CHEBI:8198) has functional parent trans-resveratrol (CHEBI:45713)
resveratrol-3-O-sulfate (CHEBI:84040) has functional parent trans-resveratrol (CHEBI:45713)
Synonyms Sources
(E)-5-(2-(4-hydroxyphenyl)ethenyl)-1,3-benzenediol ChemIDplus
(E)-resveratrol ChEBI
3,4',5-stilbenetriol ChemIDplus
3,4',5-trihydroxy-trans-stilbene MetaCyc
3,4',5-trihydroxystilbene ChemIDplus
3,5,4'-trihydroxystilbene ChemIDplus
5-[(E)-2-(4-hydroxyphenyl)vinyl]benzene-1,3-diol PDBeChem
trans-resveratrol UniProt
Manual Xrefs Databases
C00002903 KNApSAcK
CPD-83 MetaCyc
DB02709 DrugBank
HMDB0003747 HMDB
Resveratrol Wikipedia
View more database links
Registry Numbers Types Sources
1912434 Beilstein Registry Number Beilstein
1912434 Reaxys Registry Number Reaxys
501-36-0 CAS Registry Number ChemIDplus
501-36-0 CAS Registry Number NIST Chemistry WebBook
Citations Waiting for Citations Types Sources
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Last Modified
10 November 2017