CHEBI:17745 - coniferol

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ChEBI Name coniferol
Definition A phenylpropanoid that is one of the main monolignols, produced by the reduction of the carboxy functional group in cinnamic acid and the addition of a hydroxy and a methoxy substituent to the aromatic ring.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:14016, CHEBI:14017, CHEBI:4730, CHEBI:23371, CHEBI:3858
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Formula C10H12O3
Net Charge 0
Average Mass 180.203
Monoisotopic Mass 180.07864
InChI InChI=1S/C10H12O3/c1-13-10-7-8(3-2-6-11)4-5-9(10)12/h2-5,7,11-12H,6H2,1H3/b3-2+
Metabolite of Species Details
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Brassica napus (NCBI:txid3708) Found in leaf lamina (BTO:0000719). From MetaboLights See: MetaboLights Study
Apis mellifera ligustica (NCBI:txid7469) See: PubMed
Roles Classification
Biological Role(s): monolignol
A metabolite of plant origin (phytochemical) which acts as a source material for biosynthesis of both lignans and lignin.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
A semiochemical used in olfactory communication between organisms of the same species eliciting a change in sexual or social behaviour.
animal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in animals that include diverse creatures from sponges, insects to mammals.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
volatile oil component
Any plant metabolite that is found naturally as a component of a volatile oil.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing coniferol (CHEBI:17745) has functional parent (E)-cinnamyl alcohol (CHEBI:33227)
coniferol (CHEBI:17745) has role animal metabolite (CHEBI:75767)
coniferol (CHEBI:17745) has role monolignol (CHEBI:64477)
coniferol (CHEBI:17745) has role mouse metabolite (CHEBI:75771)
coniferol (CHEBI:17745) has role pheromone (CHEBI:26013)
coniferol (CHEBI:17745) has role plant metabolite (CHEBI:76924)
coniferol (CHEBI:17745) has role volatile oil component (CHEBI:27311)
coniferol (CHEBI:17745) is a guaiacols (CHEBI:134251)
coniferol (CHEBI:17745) is a phenylpropanoid (CHEBI:26004)
Incoming trans-coniferyl alcohol diacetate (CHEBI:86578) has functional parent coniferol (CHEBI:17745)
buddlenol B (CHEBI:86632) has functional parent coniferol (CHEBI:17745)
coniferin (CHEBI:16220) has functional parent coniferol (CHEBI:17745)
coniferyl p-coumarate (CHEBI:86599) has functional parent coniferol (CHEBI:17745)
coniferyl acetate (CHEBI:47905) has functional parent coniferol (CHEBI:17745)
coniferyl benzoate (CHEBI:86598) has functional parent coniferol (CHEBI:17745)
coniferyl ester (CHEBI:64292) has functional parent coniferol (CHEBI:17745)
dehydrodiconiferyl alcohol (CHEBI:91184) has functional parent coniferol (CHEBI:17745)
glycosmisic acid (CHEBI:91209) has functional parent coniferol (CHEBI:17745)
guaiacyl lignin (CHEBI:64475) has functional parent coniferol (CHEBI:17745)
guaiacylglycerol β-coniferyl ether (CHEBI:91172) has functional parent coniferol (CHEBI:17745)
pinoresinol (CHEBI:8225) has functional parent coniferol (CHEBI:17745)
simulanol (CHEBI:86940) has functional parent coniferol (CHEBI:17745)
Synonyms Sources
(E)-coniferol UniProt
4-(3-Hydroxy-1-propenyl)-2-methoxyphenol KEGG COMPOUND
4-(3-hydroxy-1-propenyl)-2-methoxyphenol ChEBI
4-[(1E)-3-hydroxy-1-propenyl]-2-methoxyphenol NIST Chemistry WebBook
Coniferyl alcohol KEGG COMPOUND
trans-coniferol HMDB
trans-coniferyl alcohol HMDB
Manual Xrefs Databases
C00000614 KNApSAcK
Coniferyl_alcohol Wikipedia
FDB015496 FooDB
HMDB0012915 HMDB
N7I PDBeChem
View more database links
Registry Numbers Types Sources
2048963 Reaxys Registry Number Reaxys
2048963 Beilstein Registry Number Beilstein
458-35-5 CAS Registry Number KEGG COMPOUND
458-35-5 CAS Registry Number ChemIDplus
458-35-5 CAS Registry Number NIST Chemistry WebBook
Citations Waiting for Citations Types Sources
11430982 PubMed citation Europe PMC
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Last Modified
30 June 2020