CHEBI:64555 - trans-p-coumaryl alcohol

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ChEBI Name trans-p-coumaryl alcohol
ChEBI ID CHEBI:64555
ChEBI ASCII Name trans-p-coumaryl alcohol
Definition 4-Hydroxycinnamyl alcohol with E-configuration of the propenyl double bond. It is one of the main monolignols.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C9H10O2
Net Charge 0
Average Mass 150.17450
Monoisotopic Mass 150.068
InChI InChI=1S/C9H10O2/c10-7-1-2-8-3-5-9(11)6-4-8/h1-6,10-11H,7H2/b2-1+
InChIKey PTNLHDGQWUGONS-OWOJBTEDSA-N
SMILES OC\C=C\c1ccc(O)cc1
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.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
(via 4-hydroxycinnamyl alcohol )
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ChEBI Ontology
Outgoing trans-p-coumaryl alcohol (CHEBI:64555) has functional parent (E)-cinnamyl alcohol (CHEBI:33227)
trans-p-coumaryl alcohol (CHEBI:64555) has role monolignol (CHEBI:64477)
trans-p-coumaryl alcohol (CHEBI:64555) is a 4-hydroxycinnamyl alcohol (CHEBI:28386)
trans-p-coumaryl alcohol (CHEBI:64555) is a phenols (CHEBI:33853)
trans-p-coumaryl alcohol (CHEBI:64555) is a phenylpropanoid (CHEBI:26004)
Incoming 4-hydroxy cinnamyl alcohol diacetate (CHEBI:86565) has functional parent trans-p-coumaryl alcohol (CHEBI:64555)
p-hydroxyphenyl lignin (CHEBI:64474) has functional parent trans-p-coumaryl alcohol (CHEBI:64555)
trans-coumaryl acetate (CHEBI:73346) has functional parent trans-p-coumaryl alcohol (CHEBI:64555)
IUPAC Name
4-[(1E)-3-hydroxyprop-1-en-1-yl]phenol
Synonyms Sources
(E)-4-coumaryl alcohol UniProt
4-Hydroxycinnamyl alcohol KEGG COMPOUND
p-Coumaryl alcohol KEGG COMPOUND
Manual Xrefs Databases
C00000613 KNApSAcK
C02646 KEGG COMPOUND
Paracoumaryl_alcohol Wikipedia
View more database links
Registry Numbers Types Sources
2961090 Reaxys Registry Number Reaxys
3690-05-9 CAS Registry Number KEGG COMPOUND
Last Modified
21 July 2015