Can act as a competitive inhibitor of certain phenylpropanoid enzymes
[1]
Poor water solubility
Chemical instability
Potent antioxidant activity
Bioactive properties
[2]
Intermediate in monolignol and lignin biosynthesis
Precursor of guaiacyl (G) and syringyl (S) lignin units
Regulates metabolic flux in phenylpropanoid pathways
[1]
Pharmaceutical and nutraceutical applications (as a promising candidate)
[2]
Classification by use
Chemicals used as biochemical pathway intermediates
Chemicals used in plant secondary metabolism studies
[1]
Bioactive compound
Pharmaceutical/nutraceutical ingredient
[2]
A trustworthy factory and manufacturer
[Cite:1] 4-Coumaroyl and Caffeoyl Shikimic Acids Inhibit 4-Coumaric Acid:Coenzyme A Ligases and Modulate Metabolic Flux for 3-Hydroxylation in Monolignol Biosynthesis of Populus trichocarpa, Moleculor Plant, Volume 8, Issue 1, 5 January 2015, Pages 176-187
[Cite:2] Supramolecular characterization of reaction product of quercetin and caffeic acid with laccase and DFT approach, Journal of Molecular Structure, Volume 1351, Part 2, 5 February 2026, 144357