Jo, Cheo-Run, Jeong, Ill-Yun, Lee, Na-Young, Kim, Kwan-Soo, Byun, Myung-Woo
언어
한국어(KOR)
URL
https://www.earticle.net/Article/A78984
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원문정보
초록
영어
Octadeca-9,12-dienyl-3,4,5-hydroxybenzoate (GA-LA) was chemically synthesized from gallic acid and linoleic acid ester, and its biological functions were tested. Radical-scavenging activity of GA-LA was comparable to those of gallic and ascorbic acids at 0.24 mM, and tyrosinase inhibition effect was higher than that of ascorbic acid. Gallic and linoleic acids did not show any tyrosinase activity. Results of cyclooxygenase (COX) inhibition effect indicate GA-LA has higher selectivity in COX-1 inhibition. GA-LA from gallic and linoleic acids could be used as functional reagent for antioxidative, skin-whitening, and anti-inflammatory effects in food, pharmaceutrical, and cosmetic industries.
목차
Abstract Introduction Materials and Methods Results and Discussion Acknowledgments References
Jo, Cheo-Run [ Radiation Food Science and Biotechnology Team, Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute ]
Jeong, Ill-Yun [ Radiation Food Science and Biotechnology Team, Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute ]
Lee, Na-Young [ Radiation Food Science and Biotechnology Team, Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute ]
Kim, Kwan-Soo [ Department of Food Science & Nutrition, Chosun University ]
Byun, Myung-Woo [ Radiation Food Science and Biotechnology Team, Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute ]
Corresponding author