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Volumn 44, Issue 7, 2008, Pages 1394-1405

Determining radical penetration of lipid bilayers with new lipophilic spin traps

Author keywords

13C NMR; DMPC; DMPO derivatives; ET(30); ESR; Free radicals; Liposome; Membrane; PBN derivatives; Spin trap; Water lipid interface

Indexed keywords

ACYLGLYCEROL LIPASE; HYDROGEN; HYDROXYL RADICAL; METHYL GROUP; NITRONE DERIVATIVE;

EID: 40949147478     PISSN: 08915849     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.freeradbiomed.2007.12.028     Document Type: Article
Times cited : (46)

References (82)
  • 1
    • 0018023094 scopus 로고
    • The formation of free radicals and the consequences of their reactions in vivo
    • Pryor W.A. The formation of free radicals and the consequences of their reactions in vivo. Photochem. Photobiol. 28 (1978) 787-801
    • (1978) Photochem. Photobiol. , vol.28 , pp. 787-801
    • Pryor, W.A.1
  • 2
    • 0000524003 scopus 로고
    • Antioxidants vs. aging
    • Packer L., and Walton J. Antioxidants vs. aging. Chemtech. 7 (1977) 276-481
    • (1977) Chemtech. , vol.7 , pp. 276-481
    • Packer, L.1    Walton, J.2
  • 3
    • 0009126944 scopus 로고
    • Biochemical consequences of lipid peroxidation
    • Bland J. Biochemical consequences of lipid peroxidation. J. Chem. Educ. 55 (1978) 151-155
    • (1978) J. Chem. Educ. , vol.55 , pp. 151-155
    • Bland, J.1
  • 4
    • 0022529172 scopus 로고
    • Oxygen free radicals and iron in relation to biology and medicine: some problems and concepts
    • Halliwell B., and Gutteridge J.M.C. Oxygen free radicals and iron in relation to biology and medicine: some problems and concepts. Arch. Biochem. Biophys. 246 (1986) 501-514
    • (1986) Arch. Biochem. Biophys. , vol.246 , pp. 501-514
    • Halliwell, B.1    Gutteridge, J.M.C.2
  • 5
    • 0029824431 scopus 로고    scopus 로고
    • Antioxidants in human health and disease
    • Halliwell B. Antioxidants in human health and disease. Annu. Rev. Nutr. 16 (1996) 33-50
    • (1996) Annu. Rev. Nutr. , vol.16 , pp. 33-50
    • Halliwell, B.1
  • 6
    • 0033015743 scopus 로고    scopus 로고
    • The aging paradox: free radical theory of aging
    • Ashok B.T., and Ali R. The aging paradox: free radical theory of aging. Exp. Gerontol. 34 (1999) 293-303
    • (1999) Exp. Gerontol. , vol.34 , pp. 293-303
    • Ashok, B.T.1    Ali, R.2
  • 7
    • 0029883764 scopus 로고    scopus 로고
    • The role of oxidized lipoproteins in atherogenesis
    • Berliner J.A., and Heinecke J.W. The role of oxidized lipoproteins in atherogenesis. Free Radic. Biol. Med. 20 (1996) 707-727
    • (1996) Free Radic. Biol. Med. , vol.20 , pp. 707-727
    • Berliner, J.A.1    Heinecke, J.W.2
  • 8
    • 0024360928 scopus 로고
    • Increased lipid peroxidation in malignant tissues of patients with colorectal cancer
    • Otamiri T., and Sjodahl R. Increased lipid peroxidation in malignant tissues of patients with colorectal cancer. Cancer 64 (1989) 422-425
    • (1989) Cancer , vol.64 , pp. 422-425
    • Otamiri, T.1    Sjodahl, R.2
  • 9
    • 0023177955 scopus 로고
    • Leukotrienes and lipoxins: structures, biosynthesis, and biological effects
    • Samuelsson B., Dahlen S.E., Lindgren J., Rouzer C.A., and Serhan C.N. Leukotrienes and lipoxins: structures, biosynthesis, and biological effects. Science 237 (1987) 1171-1176
    • (1987) Science , vol.237 , pp. 1171-1176
    • Samuelsson, B.1    Dahlen, S.E.2    Lindgren, J.3    Rouzer, C.A.4    Serhan, C.N.5
  • 10
    • 0031741551 scopus 로고    scopus 로고
    • Free radicals: their history and current status in aging and disease
    • Knight J.A. Free radicals: their history and current status in aging and disease. Ann. Clin. Lab. Sci. 28 (1998) 331-346
    • (1998) Ann. Clin. Lab. Sci. , vol.28 , pp. 331-346
    • Knight, J.A.1
  • 11
    • 0031705797 scopus 로고    scopus 로고
    • Inhibitors of lipoxygenase: a new class of cancer chemopreventive agents
    • Rioux N., and Castonguay A. Inhibitors of lipoxygenase: a new class of cancer chemopreventive agents. Carcinogenesis 19 (1998) 1393-1400
    • (1998) Carcinogenesis , vol.19 , pp. 1393-1400
    • Rioux, N.1    Castonguay, A.2
  • 12
    • 33845373509 scopus 로고
    • Mechanisms for the autoxidation of polyunsaturated lipids
    • Porter N.A. Mechanisms for the autoxidation of polyunsaturated lipids. Acc. Chem. Res. 19 (1986) 262-268
    • (1986) Acc. Chem. Res. , vol.19 , pp. 262-268
    • Porter, N.A.1
  • 13
    • 0033588022 scopus 로고    scopus 로고
    • Lipoxygenases: occurrence, functions, catalysis, and acquisition of substrate
    • Brash A.R. Lipoxygenases: occurrence, functions, catalysis, and acquisition of substrate. J. Biol. Chem. 274 (1999) 23679-23682
    • (1999) J. Biol. Chem. , vol.274 , pp. 23679-23682
    • Brash, A.R.1
  • 14
    • 0027246677 scopus 로고
    • The three-dimensional structure of an arachidonic acid 15-lipoxygenase
    • Boyington J.C., Gaffney B.J., and Amzel L.M. The three-dimensional structure of an arachidonic acid 15-lipoxygenase. Science 260 (1993) 1482-1486
    • (1993) Science , vol.260 , pp. 1482-1486
    • Boyington, J.C.1    Gaffney, B.J.2    Amzel, L.M.3
  • 16
    • 0027459113 scopus 로고
    • Mechanisms and biological relevance of lipid peroxidation initiation
    • Dix T.A., and Aikens J. Mechanisms and biological relevance of lipid peroxidation initiation. Chem. Res. Toxicol. 6 (1993) 2-18
    • (1993) Chem. Res. Toxicol. , vol.6 , pp. 2-18
    • Dix, T.A.1    Aikens, J.2
  • 17
    • 0029923359 scopus 로고    scopus 로고
    • Can superoxide organic chemistry be observed within the liposomal bilayer?
    • Frimer A.A., Strul G., Buch J., and Gottlieb H.E. Can superoxide organic chemistry be observed within the liposomal bilayer?. Free Radic. Biol. Med. 20 (1996) 843-852
    • (1996) Free Radic. Biol. Med. , vol.20 , pp. 843-852
    • Frimer, A.A.1    Strul, G.2    Buch, J.3    Gottlieb, H.E.4
  • 18
    • 0036532431 scopus 로고    scopus 로고
    • Superoxide organic chemistry within the liposomal bilayer. Part II. A correlation between location and chemistry
    • Afri M., Gotlieb H.E., and Frimer A.A. Superoxide organic chemistry within the liposomal bilayer. Part II. A correlation between location and chemistry. Free Radic. Biol. Med. 32 (2002) 605-618
    • (2002) Free Radic. Biol. Med. , vol.32 , pp. 605-618
    • Afri, M.1    Gotlieb, H.E.2    Frimer, A.A.3
  • 19
    • 0023505008 scopus 로고
    • Spin trapping: ESR parameters of spin adducts
    • Buettner G.R. Spin trapping: ESR parameters of spin adducts. Free Radic. Biol. Med. 3 (1987) 259-303
    • (1987) Free Radic. Biol. Med. , vol.3 , pp. 259-303
    • Buettner, G.R.1
  • 20
    • 0028332745 scopus 로고
    • 13C), for enhanced radical addend recognition and spin adduct persistence
    • 13C), for enhanced radical addend recognition and spin adduct persistence. J. Am. Chem. Soc. (1994) 3738-3743
    • (1994) J. Am. Chem. Soc. , pp. 3738-3743
    • Janzen, E.G.1    Zhang, Y.K.2    Haire, D.L.3
  • 22
    • 0001491269 scopus 로고
    • A more efficient synthesis of DMPO-type (nitrone) spin traps
    • Haire D.L., Hilborn J.W., and Janzen E.G. A more efficient synthesis of DMPO-type (nitrone) spin traps. J. Org. Chem. 51 (1986) 4298-4300
    • (1986) J. Org. Chem. , vol.51 , pp. 4298-4300
    • Haire, D.L.1    Hilborn, J.W.2    Janzen, E.G.3
  • 23
    • 0029013876 scopus 로고
    • 5-(Diethoxyphosphoryl)-5-methyl-1-pyrroline N-oxide: a new efficient phosphorylated nitrone for the in vitro and in vivo spin trapping of oxygen-centered radicals
    • Frejavill C., Karoui H., Tuccio B., Moigne F.L., Culcasi M., Pietri S., Lauricella R., and Tordo P. 5-(Diethoxyphosphoryl)-5-methyl-1-pyrroline N-oxide: a new efficient phosphorylated nitrone for the in vitro and in vivo spin trapping of oxygen-centered radicals. J. Med. Chem. 38 (1995) 258-265
    • (1995) J. Med. Chem. , vol.38 , pp. 258-265
    • Frejavill, C.1    Karoui, H.2    Tuccio, B.3    Moigne, F.L.4    Culcasi, M.5    Pietri, S.6    Lauricella, R.7    Tordo, P.8
  • 25
    • 13844280430 scopus 로고    scopus 로고
    • Spin adduct formation from lipophilic EMPO-derived spin traps with various oxygen-and carbon-centered radicals
    • Stolze K., Udilova N., Rosenau T., Hofinger A., and Nohl H. Spin adduct formation from lipophilic EMPO-derived spin traps with various oxygen-and carbon-centered radicals. Biochem. Pharmacol. 69 (2005) 297-305
    • (2005) Biochem. Pharmacol. , vol.69 , pp. 297-305
    • Stolze, K.1    Udilova, N.2    Rosenau, T.3    Hofinger, A.4    Nohl, H.5
  • 26
    • 17044398454 scopus 로고    scopus 로고
    • Very stable superoxide radical adducts of 5-ethoxycarbonyl-3,5-dimethyl-pyrroline N-oxide (3,5-EDPO) and its derivatives
    • Stolze K., Rohr-Udilova N., Rosenau T., Stadtmuller R., and Nohl H. Very stable superoxide radical adducts of 5-ethoxycarbonyl-3,5-dimethyl-pyrroline N-oxide (3,5-EDPO) and its derivatives. Biochem. Pharmacol. 69 (2005) 1351-1361
    • (2005) Biochem. Pharmacol. , vol.69 , pp. 1351-1361
    • Stolze, K.1    Rohr-Udilova, N.2    Rosenau, T.3    Stadtmuller, R.4    Nohl, H.5
  • 27
    • 0141922904 scopus 로고    scopus 로고
    • Spin trapping of superoxide, alkyl-and lipid-derived radicals with derivatives of the spin trap EPPN
    • Stolze K., Udilova N., Rosenau T., Hofinger A., and Nohl H. Spin trapping of superoxide, alkyl-and lipid-derived radicals with derivatives of the spin trap EPPN. Biochem. Pharmacol. 66 (2003) 1717-1726
    • (2003) Biochem. Pharmacol. , vol.66 , pp. 1717-1726
    • Stolze, K.1    Udilova, N.2    Rosenau, T.3    Hofinger, A.4    Nohl, H.5
  • 28
    • 0033965592 scopus 로고    scopus 로고
    • 2-Ethoxycarbonyl-2-methyl-3,4-dihydro-2H-pyrrole-1-oxide: evaluation of the spin trapping properties
    • Olive G., Mercier A., Le Moigne F., Rockenbauer A., and Tordo P. 2-Ethoxycarbonyl-2-methyl-3,4-dihydro-2H-pyrrole-1-oxide: evaluation of the spin trapping properties. Free Radic. Biol. Med. 28 (2000) 403-408
    • (2000) Free Radic. Biol. Med. , vol.28 , pp. 403-408
    • Olive, G.1    Mercier, A.2    Le Moigne, F.3    Rockenbauer, A.4    Tordo, P.5
  • 29
    • 0029957441 scopus 로고    scopus 로고
    • Studies on the stability of oxygen radical spin adducts of a new spin trap: 5-methyl-5-phenylpyrroline-1-oxide (MPPO)
    • Jankuratri N., Kotake P., and Janzen E.G. Studies on the stability of oxygen radical spin adducts of a new spin trap: 5-methyl-5-phenylpyrroline-1-oxide (MPPO). Free Radic. Biol. Med. 21 (1996) 889-894
    • (1996) Free Radic. Biol. Med. , vol.21 , pp. 889-894
    • Jankuratri, N.1    Kotake, P.2    Janzen, E.G.3
  • 30
    • 37049078776 scopus 로고
    • Spin-trapping study of free radical penetration into liposomal membranes
    • Strul G., Frimer A.A., and Weiner L. Spin-trapping study of free radical penetration into liposomal membranes. J. Chem. Soc., Perkin 2 (1993) 2057-2059
    • (1993) J. Chem. Soc., Perkin , vol.2 , pp. 2057-2059
    • Strul, G.1    Frimer, A.A.2    Weiner, L.3
  • 31
    • 37049077410 scopus 로고
    • Determining the location of hydrophobic spin traps within liposomes
    • Strul G., Gottlieb H.E., Frimer A.A., and Weiner L. Determining the location of hydrophobic spin traps within liposomes. J. Chem. Soc., Perkin 2 (1994) 1229-1232
    • (1994) J. Chem. Soc., Perkin , vol.2 , pp. 1229-1232
    • Strul, G.1    Gottlieb, H.E.2    Frimer, A.A.3    Weiner, L.4
  • 32
    • 0035263181 scopus 로고    scopus 로고
    • Solvatochromic effects in the electronic absorption and NMR spectra of Hypericin in organic solvents and in lipid bilayers
    • Roslaniec M., Weitman H., Frimer A.A., Afri M., Freeman D., Mazur Y., and Ehrenberg B. Solvatochromic effects in the electronic absorption and NMR spectra of Hypericin in organic solvents and in lipid bilayers. Photochem. Photobiol. 73 (2001) 110-118
    • (2001) Photochem. Photobiol. , vol.73 , pp. 110-118
    • Roslaniec, M.1    Weitman, H.2    Frimer, A.A.3    Afri, M.4    Freeman, D.5    Mazur, Y.6    Ehrenberg, B.7
  • 33
    • 3042550192 scopus 로고    scopus 로고
    • Active oxygen chemistry within the liposomal bilayer. Part III. Locating vitamin E, ubiquinol and ubiquinone and their derivatives in the lipid bilayer
    • Afri M., Ehrenberg B., Talmon Y., Schmidt J., Cohen Y., and Frimer A.A. Active oxygen chemistry within the liposomal bilayer. Part III. Locating vitamin E, ubiquinol and ubiquinone and their derivatives in the lipid bilayer. Chem. Phys. Lipids 131 (2004) 107-121
    • (2004) Chem. Phys. Lipids , vol.131 , pp. 107-121
    • Afri, M.1    Ehrenberg, B.2    Talmon, Y.3    Schmidt, J.4    Cohen, Y.5    Frimer, A.A.6
  • 34
    • 3042588253 scopus 로고    scopus 로고
    • Active oxygen chemistry within the liposomal bilayer. Part IV. Locating 2′,7′-dichlorofluorescein (DCF), 2′,7′-dichlorodihydrofluorescein (DCFH) and 2′,7′-dichlorodihydrofluorescein diacetate (DCFH-DA) in the lipid bilayer
    • Afri M., Frimer A.A., and Cohen Y. Active oxygen chemistry within the liposomal bilayer. Part IV. Locating 2′,7′-dichlorofluorescein (DCF), 2′,7′-dichlorodihydrofluorescein (DCFH) and 2′,7′-dichlorodihydrofluorescein diacetate (DCFH-DA) in the lipid bilayer. Chem. Phys. Lipids 131 (2004) 123-133
    • (2004) Chem. Phys. Lipids , vol.131 , pp. 123-133
    • Afri, M.1    Frimer, A.A.2    Cohen, Y.3
  • 35
    • 4143050094 scopus 로고    scopus 로고
    • Porphyrin depth in lipid bilayers as determined by iodide and parallax fluorescence quenching methods and its effect on photosensitizing efficiency
    • Bronshtein I., Afri M., Weitman H., Frimer A.A., Smith K.M., and Ehrenberg B. Porphyrin depth in lipid bilayers as determined by iodide and parallax fluorescence quenching methods and its effect on photosensitizing efficiency. Biophys. J. 87 (2004) 1155-1164
    • (2004) Biophys. J. , vol.87 , pp. 1155-1164
    • Bronshtein, I.1    Afri, M.2    Weitman, H.3    Frimer, A.A.4    Smith, K.M.5    Ehrenberg, B.6
  • 36
    • 0024356885 scopus 로고
    • Locating spin traps in heterogeneous media by carbon-13 NMR spectroscopy: investigations in SDS micelles, DMPC vesicles, and rat liver microsomes
    • Janzen E.J., Haire D.L., Coulter G.A., Stronks H.J., Krygsman P.H., Tower R.A., and Hilborn J.W. Locating spin traps in heterogeneous media by carbon-13 NMR spectroscopy: investigations in SDS micelles, DMPC vesicles, and rat liver microsomes. J. Org. Chem. 54 (1989) 2915-2920
    • (1989) J. Org. Chem. , vol.54 , pp. 2915-2920
    • Janzen, E.J.1    Haire, D.L.2    Coulter, G.A.3    Stronks, H.J.4    Krygsman, P.H.5    Tower, R.A.6    Hilborn, J.W.7
  • 37
    • 84989103156 scopus 로고
    • NMR solvent effect study of pyrroline-N-oxide spin traps: microenvironments in sodium dodecyl sulfate micelles
    • Haire D.L., Janzen E.G., Robinson V.J., and Zhang Y.K. NMR solvent effect study of pyrroline-N-oxide spin traps: microenvironments in sodium dodecyl sulfate micelles. Magn. Reson. Chem. 33 (1995) 796-802
    • (1995) Magn. Reson. Chem. , vol.33 , pp. 796-802
    • Haire, D.L.1    Janzen, E.G.2    Robinson, V.J.3    Zhang, Y.K.4
  • 38
    • 33947484811 scopus 로고
    • 13C chemical shift of the carbonyl group of acetone
    • 13C chemical shift of the carbonyl group of acetone. J. Am. Chem. Soc. 85 (1963) 3903-3904
    • (1963) J. Am. Chem. Soc. , vol.85 , pp. 3903-3904
    • Maciel, G.H.1    Ruben, Z.C.2
  • 39
    • 0003132171 scopus 로고
    • The effects of solvents on carbon-13 chemical shifts of the carbonyl carbon system
    • Ueji S., and Makamaura M. The effects of solvents on carbon-13 chemical shifts of the carbonyl carbon system. Tetrahedron Lett. (1976) 2549-2552
    • (1976) Tetrahedron Lett. , pp. 2549-2552
    • Ueji, S.1    Makamaura, M.2
  • 40
    • 36849120543 scopus 로고
    • Carbon-13 chemical shifts of the carbonyl group. III. Solvent effects
    • Maciel G.H., and Natterstad J.J. Carbon-13 chemical shifts of the carbonyl group. III. Solvent effects. J. Chem. Phys. 42 (1965) 2752-2759
    • (1965) J. Chem. Phys. , vol.42 , pp. 2752-2759
    • Maciel, G.H.1    Natterstad, J.J.2
  • 41
    • 0000121690 scopus 로고
    • The water content of a micelle interior: the fjord vs. reef models
    • Menger F.M., Jercunica J.M., and Johnson J.C. The water content of a micelle interior: the fjord vs. reef models. J. Am. Chem. Soc. 100 (1978) 4676-4678
    • (1978) J. Am. Chem. Soc. , vol.100 , pp. 4676-4678
    • Menger, F.M.1    Jercunica, J.M.2    Johnson, J.C.3
  • 42
    • 33845560336 scopus 로고
    • The structure of micelles
    • Menger F.M. The structure of micelles. Acc. Chem. Res. 12 (1979) 111-117
    • (1979) Acc. Chem. Res. , vol.12 , pp. 111-117
    • Menger, F.M.1
  • 44
    • 0002280065 scopus 로고
    • Empirical parameters of solvent polarity
    • Reichardt C. Empirical parameters of solvent polarity. Angew. Chem., Int. Ed. Engl. 4 (1965) 30-40
    • (1965) Angew. Chem., Int. Ed. Engl. , vol.4 , pp. 30-40
    • Reichardt, C.1
  • 45
    • 5844252510 scopus 로고
    • Solvatochromic dyes as solvent polarity indicators
    • Reichardt C. Solvatochromic dyes as solvent polarity indicators. Chem. Rev. 94 (1994) 2319-2358
    • (1994) Chem. Rev. , vol.94 , pp. 2319-2358
    • Reichardt, C.1
  • 46
    • 0002436816 scopus 로고
    • Model of singlet oxygen scavenging by α-tocopherol in biomembranes
    • Fragata M., and Bellemare F. Model of singlet oxygen scavenging by α-tocopherol in biomembranes. Chem. Phys. Lipids 27 (1980) 93-99
    • (1980) Chem. Phys. Lipids , vol.27 , pp. 93-99
    • Fragata, M.1    Bellemare, F.2
  • 47
    • 0015454947 scopus 로고
    • Differences between conformations of lecithin and phosphatidylethanolamine polar groups and their effects on interactions of phospholipid bilayer membranes
    • Phillips M.C., Finer E.G., and Houser H. Differences between conformations of lecithin and phosphatidylethanolamine polar groups and their effects on interactions of phospholipid bilayer membranes. Biochem. Biophys. Acta 290 (1972) 397-402
    • (1972) Biochem. Biophys. Acta , vol.290 , pp. 397-402
    • Phillips, M.C.1    Finer, E.G.2    Houser, H.3
  • 49
    • 0001631248 scopus 로고
    • Synthesis and spin-trapping kinetics of new alkyl-substituted cyclic nitrones
    • Haire D.L., and Janzen E.G. Synthesis and spin-trapping kinetics of new alkyl-substituted cyclic nitrones. Can. J. Chem. (1982) 1514-1522
    • (1982) Can. J. Chem. , pp. 1514-1522
    • Haire, D.L.1    Janzen, E.G.2
  • 50
    • 33751554764 scopus 로고
    • Monolayer transformation by nucleophilic substitution: applications to the creation of new monolayer assemblies
    • Balachander N., and Sukenik C.N. Monolayer transformation by nucleophilic substitution: applications to the creation of new monolayer assemblies. Langmuir 16 (1990) 1621-1627
    • (1990) Langmuir , vol.16 , pp. 1621-1627
    • Balachander, N.1    Sukenik, C.N.2
  • 52
    • 3042856792 scopus 로고    scopus 로고
    • Exceptionally long-range self-assembly of hexa-peri-hexabenzocoronene with dove-tailed alkyl substituents
    • Pisula W., Kastler M., Wasserfallen D., Pakula T., and Mullen K. Exceptionally long-range self-assembly of hexa-peri-hexabenzocoronene with dove-tailed alkyl substituents. J. Am. Chem. Soc. 126 (2004) 8074-8075
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 8074-8075
    • Pisula, W.1    Kastler, M.2    Wasserfallen, D.3    Pakula, T.4    Mullen, K.5
  • 53
    • 33751499282 scopus 로고
    • Chemistry of micelles. 18. Cascade polymers: syntheses and characterization of one-directional arborols based on adamantane
    • Newkom G.R., Behera R.K., Moorefield C.N., and Baker G.R. Chemistry of micelles. 18. Cascade polymers: syntheses and characterization of one-directional arborols based on adamantane. J. Org. Chem. 56 (1991) 7162-7167
    • (1991) J. Org. Chem. , vol.56 , pp. 7162-7167
    • Newkom, G.R.1    Behera, R.K.2    Moorefield, C.N.3    Baker, G.R.4
  • 54
    • 0001719679 scopus 로고
    • On etherification
    • Williamson A.W. On etherification. J. Chem. Soc. 4 (1852) 229-234
    • (1852) J. Chem. Soc. , vol.4 , pp. 229-234
    • Williamson, A.W.1
  • 57
    • 0000659131 scopus 로고
    • Facile one-step synthesis of phenyl-tert-butylnitrone (PBN) and its derivatives
    • Huie R., and Cherry W.R. Facile one-step synthesis of phenyl-tert-butylnitrone (PBN) and its derivatives. J. Org. Chem. 50 (1985) 1531-1532
    • (1985) J. Org. Chem. , vol.50 , pp. 1531-1532
    • Huie, R.1    Cherry, W.R.2
  • 58
    • 37049144181 scopus 로고
    • For a similar reaction, see: Work, T. S. Synthesis of N-trimethylglycylcholine
    • For a similar reaction, see: Work, T. S. Synthesis of N-trimethylglycylcholine. J. Chem. Soc. (1941) 190-191
    • (1941) J. Chem. Soc. , pp. 190-191
  • 62
    • 40949154179 scopus 로고    scopus 로고
    • Cohen, Y., Afri, M., Frimer, A. A. (submitted for review).
    • Cohen, Y., Afri, M., Frimer, A. A. (submitted for review).
  • 63
    • 40949148471 scopus 로고    scopus 로고
    • Cohen, Y. Ramat Gan: Bar-Ilan Univ., 2005. [Ph.D. thesis]
    • Cohen, Y. Ramat Gan: Bar-Ilan Univ., 2005. [Ph.D. thesis]
  • 64
    • 18544384019 scopus 로고
    • Oxidation of tartaric acid in presence of iron
    • Fenton H.J.H. Oxidation of tartaric acid in presence of iron. J. Chem. Soc. 65 (1894) 899-910
    • (1894) J. Chem. Soc. , vol.65 , pp. 899-910
    • Fenton, H.J.H.1
  • 65
    • 1542789741 scopus 로고
    • Fenton's reagent revisited
    • Walling C. Fenton's reagent revisited. Acc. Chem. Res. 8 (1975) 125-131
    • (1975) Acc. Chem. Res. , vol.8 , pp. 125-131
    • Walling, C.1
  • 66
    • 40949139163 scopus 로고    scopus 로고
    • See the collection of articles in: Oberley, L. W., ed. Superoxide dismutase. Boca Raton, FL: CRC Press, Vols. 1 and 2, 1982, Vol. 3, 1985.
    • See the collection of articles in: Oberley, L. W., ed. Superoxide dismutase. Boca Raton, FL: CRC Press, Vols. 1 and 2, 1982, Vol. 3, 1985.
  • 69
    • 0031035450 scopus 로고    scopus 로고
    • The origin of the hydroxyl radical oxygen in the Fenton reaction
    • Lloyd R.V., Hanna P.M., and Mason R.P. The origin of the hydroxyl radical oxygen in the Fenton reaction. Free Radic. Biol. Med. 22 (1997) 885-888
    • (1997) Free Radic. Biol. Med. , vol.22 , pp. 885-888
    • Lloyd, R.V.1    Hanna, P.M.2    Mason, R.P.3
  • 70
    • 0001053910 scopus 로고
    • The reaction of OH radicals with dimethyl sulfoxide: a comparative study of Fenton's reagent and the radiolysis of aqueous dimethyl sulfoxide solutions
    • Eberhardt M.K., and Colina R. The reaction of OH radicals with dimethyl sulfoxide: a comparative study of Fenton's reagent and the radiolysis of aqueous dimethyl sulfoxide solutions. J. Org. Chem. 53 (1988) 1071-1074
    • (1988) J. Org. Chem. , vol.53 , pp. 1071-1074
    • Eberhardt, M.K.1    Colina, R.2
  • 71
    • 0004516807 scopus 로고
    • Trapping of short-lived free radicals as nitroxide radicals detectable by E.S.R. spectroscopy: the radicals formed in the reactions between OH radicals and some sulfoxides and sulfones
    • Lagercrantz C., and Forshult S. Trapping of short-lived free radicals as nitroxide radicals detectable by E.S.R. spectroscopy: the radicals formed in the reactions between OH radicals and some sulfoxides and sulfones. Acta Chem. Scand. 23 (1969) 811-817
    • (1969) Acta Chem. Scand. , vol.23 , pp. 811-817
    • Lagercrantz, C.1    Forshult, S.2
  • 72
    • 0016862807 scopus 로고
    • Current concepts concerning radioprotective and cryoprotective properties of dimethyl sulfoxide in cellular systems
    • Ashwood-Smith M.J. Current concepts concerning radioprotective and cryoprotective properties of dimethyl sulfoxide in cellular systems. Ann. N. Y. Acad. Sci. 243 (1975) 246-256
    • (1975) Ann. N. Y. Acad. Sci. , vol.243 , pp. 246-256
    • Ashwood-Smith, M.J.1
  • 73
    • 0018783007 scopus 로고
    • Chemical evidence for production of hydroxyl radicals during microsomal electron transfer
    • Cohen G., and Cederbaum A.J. Chemical evidence for production of hydroxyl radicals during microsomal electron transfer. Science 204 (1979) 66-68
    • (1979) Science , vol.204 , pp. 66-68
    • Cohen, G.1    Cederbaum, A.J.2
  • 74
    • 0020048321 scopus 로고
    • Production of hydroxyl radical by decomposition of superoxide spin-trapped adducts
    • Finkelstein E., Rosen G.M., and Rauckman E.J. Production of hydroxyl radical by decomposition of superoxide spin-trapped adducts. Mol. Pharmacol. 21 (1982) 262-265
    • (1982) Mol. Pharmacol. , vol.21 , pp. 262-265
    • Finkelstein, E.1    Rosen, G.M.2    Rauckman, E.J.3
  • 75
    • 33847087667 scopus 로고
    • Spin trapping: kinetics of the reaction of superoxide and hydroxyl radicals with nitrones
    • Finkelstein E., Rosen G.M., and Rauckman E.J. Spin trapping: kinetics of the reaction of superoxide and hydroxyl radicals with nitrones. J. Am. Chem. Soc. 102 (1980) 4994-4999
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 4994-4999
    • Finkelstein, E.1    Rosen, G.M.2    Rauckman, E.J.3
  • 76
    • 0018992113 scopus 로고
    • Spin trapping of superoxide and hydroxyl radical: practical aspects
    • Finkelstein E., Rosen G.M., and Rauckman E.J. Spin trapping of superoxide and hydroxyl radical: practical aspects. Arch. Biochem. Biophys. 200 (1980) 1-16
    • (1980) Arch. Biochem. Biophys. , vol.200 , pp. 1-16
    • Finkelstein, E.1    Rosen, G.M.2    Rauckman, E.J.3
  • 77
    • 0001718625 scopus 로고
    • Substituent effects in the kinetic analysis of free-radical reactions with nitrone spin traps
    • Greenstock C.L., and Wiebe R.H. Substituent effects in the kinetic analysis of free-radical reactions with nitrone spin traps. Can. J. Chem. 60 (1982) 1560-1564
    • (1982) Can. J. Chem. , vol.60 , pp. 1560-1564
    • Greenstock, C.L.1    Wiebe, R.H.2
  • 78
    • 0036391214 scopus 로고    scopus 로고
    • Substituent effect on the rate of the hydroxyl and phenyl radical spin trapping with nitrones
    • Sueishi Y., Yoshioka C., Olea-Azar C., Reinke L.A., and Kotake T. Substituent effect on the rate of the hydroxyl and phenyl radical spin trapping with nitrones. Bull. Chem. Soc. Jpn. 75 (2002) 2043-2047
    • (2002) Bull. Chem. Soc. Jpn. , vol.75 , pp. 2043-2047
    • Sueishi, Y.1    Yoshioka, C.2    Olea-Azar, C.3    Reinke, L.A.4    Kotake, T.5
  • 79
    • 0018783453 scopus 로고
    • Chromium oxalate: a new spin label broadening agent for use with thylakoids
    • Berg S.P., and Nesbitt D.M. Chromium oxalate: a new spin label broadening agent for use with thylakoids. Biochem. Biophys. Acta 548 (1979) 608-615
    • (1979) Biochem. Biophys. Acta , vol.548 , pp. 608-615
    • Berg, S.P.1    Nesbitt, D.M.2
  • 81
    • 0015937123 scopus 로고
    • Effect of proteins on the motion of spin-labeled fatty acids in mycoplasma membranes
    • Rottem S., and Samuni A. Effect of proteins on the motion of spin-labeled fatty acids in mycoplasma membranes. Biochim. Biophys. Acta 298 (1973) 32-38
    • (1973) Biochim. Biophys. Acta , vol.298 , pp. 32-38
    • Rottem, S.1    Samuni, A.2
  • 82
    • 33646416475 scopus 로고    scopus 로고
    • Aqueous solutions next to phospholipid membrane surfaces: insights from simulations
    • Berkowitz M.L., Bostick D.L., and Pandit S. Aqueous solutions next to phospholipid membrane surfaces: insights from simulations. Chem. Rev. 106 (2006) 1526-1539
    • (2006) Chem. Rev. , vol.106 , pp. 1526-1539
    • Berkowitz, M.L.1    Bostick, D.L.2    Pandit, S.3


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