메뉴 건너뛰기




Volumn 123, Issue 2, 2010, Pages 442-450

Antioxidation reaction mechanism studies of phenolic lignans, identification of antioxidation products of secoisolariciresinol from lipid oxidation

Author keywords

Antioxidation; Ethyl linoleate; Lignan; Peroxide; Reaction mechanism in lipid; Secoisolariciresinol

Indexed keywords

2,2' AZOBIS(ISOBUTYRONITRILE); BENZENE; ISOBUTYRONITRILE; LARICIRESINOL; LIGNAN DERIVATIVE; LINOLEIC ACID ETHYL ESTER; NITRILE; PEROXIDE; SECOISOLARICIRESINOL; UNCLASSIFIED DRUG;

EID: 77953285657     PISSN: 03088146     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.foodchem.2010.04.065     Document Type: Article
Times cited : (41)

References (34)
  • 2
    • 0020026453 scopus 로고
    • Origin of lignans in mammals and identification of precursors from plants
    • Axelson M., Sjovall J., Gustafsson B.E., and Setchell K. Origin of lignans in mammals and identification of precursors from plants. Nature 298 (1982) 656-660
    • (1982) Nature , vol.298 , pp. 656-660
    • Axelson, M.1    Sjovall, J.2    Gustafsson, B.E.3    Setchell, K.4
  • 3
    • 0027232771 scopus 로고
    • Model biomembranes: Quantitative studies of peroxidation, antioxidant action, partitioning, and oxidative stress
    • Barclay L.R.C. Model biomembranes: Quantitative studies of peroxidation, antioxidant action, partitioning, and oxidative stress. Canadian Journal of Chemistry 71 (1993) 1-16
    • (1993) Canadian Journal of Chemistry , vol.71 , pp. 1-16
    • Barclay, L.R.C.1
  • 4
    • 77953288730 scopus 로고    scopus 로고
    • Bond dissociation energies and thermodynamic functions of antioxidants
    • CRC Press, Boca Raton
    • Denisov E.T., and Denisova T.G. Bond dissociation energies and thermodynamic functions of antioxidants. Handbook of antioxidants. 2nd ed. (2000), CRC Press, Boca Raton 83-88
    • (2000) Handbook of antioxidants. 2nd ed. , pp. 83-88
    • Denisov, E.T.1    Denisova, T.G.2
  • 6
    • 33646426192 scopus 로고    scopus 로고
    • Antioxidants
    • The Oily Press, Briggwater
    • Frankel E.N. Antioxidants. Lipid oxidation. 2nd ed. (2005), The Oily Press, Briggwater 209-216
    • (2005) Lipid oxidation. 2nd ed. , pp. 209-216
    • Frankel, E.N.1
  • 8
    • 0343504858 scopus 로고
    • Metabolite derived from shikimic acid
    • Clarendon Press, Oxford
    • Mann J. Metabolite derived from shikimic acid. Secondary mtabolism (1987), Clarendon Press, Oxford 174-190
    • (1987) Secondary mtabolism , pp. 174-190
    • Mann, J.1
  • 10
    • 0035183667 scopus 로고    scopus 로고
    • Antioxidant mechanism of carnosic acid: Structural identification of two oxidation products
    • Masuda T., Inaba Y., and Takeda Y. Antioxidant mechanism of carnosic acid: Structural identification of two oxidation products. Journal of Agricultural and Food Chemistry 49 (2001) 5560-5565
    • (2001) Journal of Agricultural and Food Chemistry , vol.49 , pp. 5560-5565
    • Masuda, T.1    Inaba, Y.2    Takeda, Y.3
  • 11
    • 0034843535 scopus 로고    scopus 로고
    • Chemical studies on antioxidant mechanism of curcumin: analysis of oxidative coupling produces from curcumin and linoleate
    • Masuda T., Maekawa T., Hidaka K., Bando H., Takada Y., and Yamaguchi H. Chemical studies on antioxidant mechanism of curcumin: analysis of oxidative coupling produces from curcumin and linoleate. Journal of Agricultural and Food Chemistry 49 (2001) 2539-2547
    • (2001) Journal of Agricultural and Food Chemistry , vol.49 , pp. 2539-2547
    • Masuda, T.1    Maekawa, T.2    Hidaka, K.3    Bando, H.4    Takada, Y.5    Yamaguchi, H.6
  • 12
  • 13
    • 4043146489 scopus 로고    scopus 로고
    • Thermal recovery of antioxidant activity from carnosol quinone, the main antioxidation product of carnosol
    • Masuda T., Kirikihira T., Takeda Y., and Yonemori S. Thermal recovery of antioxidant activity from carnosol quinone, the main antioxidation product of carnosol. Journal of the Science of Food and Agriculture 84 (2004) 1421-1427
    • (2004) Journal of the Science of Food and Agriculture , vol.84 , pp. 1421-1427
    • Masuda, T.1    Kirikihira, T.2    Takeda, Y.3    Yonemori, S.4
  • 14
    • 33748419160 scopus 로고    scopus 로고
    • Antioxidant mechanism studies on ferulic acid, isolation and structure identification of the main antioxidation product from methyl ferulate
    • Masuda T., Yamada K., Maekawa T., Takeda Y., and Yamaguchi H. Antioxidant mechanism studies on ferulic acid, isolation and structure identification of the main antioxidation product from methyl ferulate. Food Science and Technology Research 12 (2006) 178-182
    • (2006) Food Science and Technology Research , vol.12 , pp. 178-182
    • Masuda, T.1    Yamada, K.2    Maekawa, T.3    Takeda, Y.4    Yamaguchi, H.5
  • 15
    • 33748429030 scopus 로고    scopus 로고
    • Antioxidant mechanism studies on ferulic acid, identification of oxidative coupling products from methyl ferulate and linoleate
    • Masuda T., Yamada K., Maekawa T., Takeda Y., and Yamaguchi H. Antioxidant mechanism studies on ferulic acid, identification of oxidative coupling products from methyl ferulate and linoleate. Journal of Agricultural and Food Chemistry 54 (2006) 6069-6074
    • (2006) Journal of Agricultural and Food Chemistry , vol.54 , pp. 6069-6074
    • Masuda, T.1    Yamada, K.2    Maekawa, T.3    Takeda, Y.4    Yamaguchi, H.5
  • 16
    • 49049101299 scopus 로고    scopus 로고
    • Antioxidation mechanism studies of caffeic acid: Identification of antioxidation products of methyl caffeate from lipid oxidation
    • Masuda T., Yamada K., Akiyama J., Someya T., Odaka Y., Takeda Y., et al. Antioxidation mechanism studies of caffeic acid: Identification of antioxidation products of methyl caffeate from lipid oxidation. Journal of Agricultural and Food Chemistry 56 (2008) 5947-5952
    • (2008) Journal of Agricultural and Food Chemistry , vol.56 , pp. 5947-5952
    • Masuda, T.1    Yamada, K.2    Akiyama, J.3    Someya, T.4    Odaka, Y.5    Takeda, Y.6
  • 18
    • 22144467376 scopus 로고    scopus 로고
    • Lignan contents of Dutch plant food: A database including lariciresinol, pinoresinol, secoisolariciresinol, and matairesinol
    • Milder I.E., Arts I.C., Putte B., Venema D.P., and Hollman P.C. Lignan contents of Dutch plant food: A database including lariciresinol, pinoresinol, secoisolariciresinol, and matairesinol. British Journal of Nutrition 93 (2005) 393-402
    • (2005) British Journal of Nutrition , vol.93 , pp. 393-402
    • Milder, I.E.1    Arts, I.C.2    Putte, B.3    Venema, D.P.4    Hollman, P.C.5
  • 20
    • 4544264733 scopus 로고    scopus 로고
    • Effect of alcoholic solvents on antiradical abilities of protocatechuic acid and its alkyl esters
    • Saito S., Okamoto Y., and Kawabata J. Effect of alcoholic solvents on antiradical abilities of protocatechuic acid and its alkyl esters. Bioscience, Biotechnology, and Biochemistry 68 (2004) 1221-1227
    • (2004) Bioscience, Biotechnology, and Biochemistry , vol.68 , pp. 1221-1227
    • Saito, S.1    Okamoto, Y.2    Kawabata, J.3
  • 22
    • 39849098275 scopus 로고    scopus 로고
    • Phenolic compounds of major oilseeds and plant oils
    • CRC Press, Boca Raton
    • Shahidi F., and Naczk M. Phenolic compounds of major oilseeds and plant oils. Phenolics in food and nutraceuticals (2004), CRC Press, Boca Raton 83-116
    • (2004) Phenolics in food and nutraceuticals , pp. 83-116
    • Shahidi, F.1    Naczk, M.2
  • 24
    • 33748188128 scopus 로고    scopus 로고
    • Phytoestrogen content of foods consumed in Canada, including isoflavones, lignans, and coumestan
    • Thompson L.U., Boucher B.A., Liu Z., Cotterchio M., and Kreiger N. Phytoestrogen content of foods consumed in Canada, including isoflavones, lignans, and coumestan. Nutrition and Cancer 54 (2006) 184-201
    • (2006) Nutrition and Cancer , vol.54 , pp. 184-201
    • Thompson, L.U.1    Boucher, B.A.2    Liu, Z.3    Cotterchio, M.4    Kreiger, N.5
  • 25
    • 13244284580 scopus 로고    scopus 로고
    • The usual intake of lignans but not that of isoflavones may be related to cardiovascular risk factors in U.S. men
    • van der Schouw Y.T., Sampson L., Willett W.C., and Rimm E.B. The usual intake of lignans but not that of isoflavones may be related to cardiovascular risk factors in U.S. men. Journal of Nutrition 135 (2005) 260-266
    • (2005) Journal of Nutrition , vol.135 , pp. 260-266
    • van der Schouw, Y.T.1    Sampson, L.2    Willett, W.C.3    Rimm, E.B.4
  • 26
    • 19544385077 scopus 로고    scopus 로고
    • Dietary lignans: potential role in cancer prevention
    • Webb A.L., and McCullough M.L. Dietary lignans: potential role in cancer prevention. Nutrition and Cancer 51 (2005) 117-131
    • (2005) Nutrition and Cancer , vol.51 , pp. 117-131
    • Webb, A.L.1    McCullough, M.L.2
  • 27
    • 0033457240 scopus 로고    scopus 로고
    • Identification of thermal decomposition products of carnosol, an antioxidant in rosemary and sage
    • Wei G.-J., Wang M., Rosen R.T., and Ho C.-T. Identification of thermal decomposition products of carnosol, an antioxidant in rosemary and sage. Journal of Food Lipids 6 (1999) 173-179
    • (1999) Journal of Food Lipids , vol.6 , pp. 173-179
    • Wei, G.-J.1    Wang, M.2    Rosen, R.T.3    Ho, C.-T.4
  • 30
    • 56749150575 scopus 로고    scopus 로고
    • Antioxidant activity of butane type lignans, secoisolariciresinol, dihydroguaiaretic acid, and 7,7′-oxodihydroguaiaretic acid
    • Yamauchi S., Masuda T., Sugahara T., Kawaguchi Y., Ohuchi M., Someya T., et al. Antioxidant activity of butane type lignans, secoisolariciresinol, dihydroguaiaretic acid, and 7,7′-oxodihydroguaiaretic acid. Bioscience, Biotechnology, and Biochemistry 72 (2008) 2981-2986
    • (2008) Bioscience, Biotechnology, and Biochemistry , vol.72 , pp. 2981-2986
    • Yamauchi, S.1    Masuda, T.2    Sugahara, T.3    Kawaguchi, Y.4    Ohuchi, M.5    Someya, T.6
  • 31
    • 0025342113 scopus 로고
    • Reaction products of α-tocopherol with methyl linoleate-peroxyl radicals
    • Yamauchi R., Matsui T., Kato K., and Ueno Y. Reaction products of α-tocopherol with methyl linoleate-peroxyl radicals. Lipid 25 (1990) 152-158
    • (1990) Lipid , vol.25 , pp. 152-158
    • Yamauchi, R.1    Matsui, T.2    Kato, K.3    Ueno, Y.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.