p-coumaric acid
Compound Overview
| Name | p-coumaric acid |
|---|---|
| IUPAC Name | (2E)-3-(4-hydroxyphenyl)prop-2-enoic acid |
| Formula | C9H8O3 |
| SMILES | C1=CC(=CC=C1C=CC(=O)O)O |
| Carbon Number | 9 |
| Molecular Weight | 164.16 |
| Polymer Type | monomer |
| Synonyms |
trans-p-coumaric acid trans-p-coumarinic acid trans-p-Hydroxycinnamate trans-p-hydroxycinnamic acid naringeninic acid 4-Hydroxycinnamic acid (E)-p-coumaric acid (E)-p-hydroxycinnamic acid p-coumarate (2E)-3-(4-hydroxyphenyl)prop-2-enoic acid |
Chemical Structure
Structure from PubChem
External Databases
Empirical Data
Organisms that can utilize this substrate (22) Empirical
Pathways Empirical
| Pathway Name | Full Name |
|---|---|
| p-coumaric acid | p-coumaric acid |
Predicted Relationships
Hide predicted
The sections below contain relationships inferred from the empirical data above. They are computationally predicted and have not been independently verified. Learn more about data assumptions →
Organisms predicted to process p-coumaric acid through a pathway Predicted
For each pathway where p-coumaric acid enters as a reactant, organisms recorded as being able to utilise it but not yet confirmed for that pathway are listed as predicted. Not experimentally verified. What does this mean?
Reactions involving p-coumaric acid
| Reaction | Role in Reaction |
|---|---|
| p-coumaric acid + CoA + ATP → p-coumaroyl-CoA + AMP + PPi | substrate |
Transporters
No transporters are currently linked to this substrate.