EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C9H10O2 |
| Net Charge | 0 |
| Average Mass | 150.177 |
| Monoisotopic Mass | 150.06808 |
| SMILES | OC/C=C/c1ccc(O)cc1 |
| 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 |
| Wikipedia |
|---|
| Roles Classification |
|---|
| Biological Roles: | 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. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| 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 Relation(s) |
| 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) |
| 4-hydroxy cinnamyl alcohol diacetate (CHEBI:86565) has functional parent trans-p-coumaryl alcohol (CHEBI:64555) |
| IUPAC Name |
|---|
| 4-[(1E)-3-hydroxyprop-1-en-1-yl]phenol |
| Synonyms | Source |
|---|---|
| 4-Hydroxycinnamyl alcohol | KEGG COMPOUND |
| p-Coumaryl alcohol | KEGG COMPOUND |
| UniProt Name | Source |
|---|---|
| (E)-4-coumaroyl alcohol | UniProt |
| Manual Xrefs | Databases |
|---|---|
| Paracoumaryl_alcohol | Wikipedia |
| C02646 | KEGG COMPOUND |
| C00000613 | KNApSAcK |
| Registry Numbers | Sources |
|---|---|
| Reaxys:2961090 | Reaxys |
| CAS:3690-05-9 | KEGG COMPOUND |