CHEBI:17745 - coniferol

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ChEBI Name coniferol
ChEBI ID CHEBI:17745
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+
InChIKey JMFRWRFFLBVWSI-NSCUHMNNSA-N
SMILES C1=C(C(=CC=C1/C=C/CO)O)OC
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).
pheromone
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)
IUPAC Name
4-[(1E)-3-hydroxyprop-1-en-1-yl]-2-methoxyphenol
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
Coniferol KEGG COMPOUND
Coniferyl alcohol KEGG COMPOUND
trans-coniferol HMDB
trans-coniferyl alcohol HMDB
Manual Xrefs Databases
C00000614 KNApSAcK
C00590 KEGG COMPOUND
CONIFERYL-ALCOHOL MetaCyc
Coniferyl_alcohol Wikipedia
FDB015496 FooDB
HMDB0012915 HMDB
N7I PDBeChem
View more database links
Registry Numbers Types Sources
2048963 Reaxys Registry Number Reaxys
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
11684179 PubMed citation Europe PMC
12676987 PubMed citation Europe PMC
20336005 PubMed citation Europe PMC
21319787 PubMed citation Europe PMC
22851762 PubMed citation Europe PMC
22920542 PubMed citation Europe PMC
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23448127 PubMed citation Europe PMC
23624856 PubMed citation Europe PMC
23633600 PubMed citation Europe PMC
23876147 PubMed citation Europe PMC
31629237 PubMed citation Europe PMC
6660881 PubMed citation Europe PMC
Last Modified
30 June 2020