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<i>p</i>‐Coumaric acid and its conjugates: dietary sources, pharmacokinetic properties and biological activities

Journal of the Science of Food and Agriculture · 2015 · Vol. 96(9) · pp. 2952–2962
Kehan PeiJuanying OuJunqing HuangShiyi Ou

Abstract

p-Coumaric acid (4-hydroxycinnamic acid) is a phenolic acid that has low toxicity in mice (LD50 = 2850 mg kg(-1) body weight), serves as a precursor of other phenolic compounds, and exists either in free or conjugated form in plants. Conjugates of p-coumaric acid have been extensively studied in recent years due to their bioactivities. In this review, the occurrence, bioavailability and bioaccessibility of p-coumaric acid and its conjugates with mono-, oligo- and polysaccharides, alkyl alcohols, organic acids, amine and lignin are discussed. Their biological activities, including antioxidant, anti-cancer, antimicrobial, antivirus, anti-inflammatory, antiplatelet aggregation, anxiolytic, antipyretic, analgesic, and anti-arthritis activities, and their mitigatory effects against diabetes, obesity, hyperlipaemia and gout are compared. Cumulative evidence from multiple studies indicates that conjugation of p-coumaric acid greatly strengthens its biological activities; however, the high biological activity but low absorption of its conjugates remains a puzzle. © 2015 Society of Chemical Industry.

Phytochemicals and Antioxidant ActivitiesEssential Oils and Antimicrobial ActivityGinkgo biloba and Cashew ApplicationsChemistryBioavailabilityp-Coumaric acidAntioxidantCoumaric acidHydroxycinnamic acidBiological activityAntimicrobialBiochemistryOrganic chemistry

MeSH terms

Diet, HealthyAgaricalesAnimalsAnti-Infective AgentsAntineoplastic Agents, PhytogenicAntioxidantsCoumaric AcidsFood PreservativesHumansHypoglycemic AgentsIntestinal AbsorptionPlants, EdiblePlants, MedicinalPropionatesDietary Supplements

Funding

  • National Cancer Institute
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