Coumaric acid

From Food & Medicine Encyclopedia

Coumaric Acid is a hydroxycinnamic acid, an organic compound that is a hydroxy derivative of cinnamic acid. There are three isomers, o-coumaric acid, m-coumaric acid, and p-coumaric acid, that differ by the position of the hydroxy substitution of the phenyl group.

Chemical Structure[edit]

Coumaric acid has the molecular formula C9H8O3. It is a crystalline solid that is slightly soluble in water. The three isomers of coumaric acid are distinguished by the position of the hydroxy group on the phenyl ring: ortho (o-), meta (m-), and para (p-).

Natural Occurrence[edit]

Coumaric acid is found in a variety of plants, including parsley, thyme, oregano, and celery. It is also found in the vinegar produced from fermented foods, such as sauerkraut and pickles.

Health Benefits[edit]

Research has suggested that coumaric acid may have antioxidant, anti-inflammatory, and anticancer properties. It may also help to prevent heart disease and diabetes.

Pharmacology[edit]

In the body, coumaric acid is metabolized into ferulic acid, another hydroxycinnamic acid with potential health benefits. The metabolism of coumaric acid involves the enzyme 4-coumarate-CoA ligase, which is involved in the biosynthesis of lignin, a complex organic polymer that is a major component of the cell walls of plants.

See Also[edit]

This article is a stub related to pharmacology. You can help WikiMD by expanding it!


Medical Disclaimer: WikiMD is for informational purposes only and is not a substitute for professional medical advice. Content may be inaccurate or outdated and should not be used for diagnosis or treatment. Always consult your healthcare provider for medical decisions. Verify information with trusted sources such as CDC.gov and NIH.gov. By using this site, you agree that WikiMD is not liable for any outcomes related to its content. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.