Correlation Engine 2.0
Clear Search sequence regions


  • amino acids (6)
  • dipeptides (6)
  • food (1)
  • food additives (2)
  • free radicals (1)
  • help (1)
  • ions (1)
  • lipid (2)
  • metal (1)
  • molecular structures (1)
  • peptides (1)
  • thiol (4)
  • tryptophan (1)
  • Sizes of these terms reflect their relevance to your search.

    In the history of modern nutritional science, understanding antioxidants is one of the major topics. In many cases, food-derived antioxidants have π conjugate or thiol group in their molecular structures because π conjugate stabilizes radical by its delocalization and two thiol groups form a disulfide bond in its antioxidative process. In recent years, antioxidant peptides have received much attention because for their ability to scavenge free radicals, inhibition of lipid peroxidation, chelation of transition metal ions, as well as their additional nutritional value. Among them, dipeptides are attracting much interest as post-amino acids, which have residues in common with amino acids, but also have different physiological properties and functions from those of amino acids. Especially, dipeptides containing moieties of several amino acid (tryptophan, tyrosine, histidine, cysteine, and methionine) possess potent antioxidant activity. This review summarizes previous details of structural property, radical scavenging activity, and biological activity of antioxidant dipeptide. Hopefully, this review will help provide a new insight into the study of the biological functions of antioxidant dipeptides.

    Citation

    Hitoshi Ozawa, Taiki Miyazawa, Gregor Carpentero Burdeos, Teruo Miyazawa. Biological Functions of Antioxidant Dipeptides. Journal of nutritional science and vitaminology. 2022;68(3):162-171

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 35768247

    View Full Text