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Volumn 9, Issue 18, 2007, Pages 3499-3502

A dual sensor spin trap for use with EPR spectroscopy

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPROPANE; CYCLOPROPANE DERIVATIVE; FREE RADICAL; NITROGEN OXIDE; NITRONES; PHENOL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 34548541533     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol071285o     Document Type: Article
Times cited : (11)

References (39)
  • 6
    • 27444435355 scopus 로고    scopus 로고
    • For a discussion of the importance and limitations of a-tocopherol as a biological antioxidant, see: Kim, H.-Y.; Pratt, D. A.; Seal, J. R.; Wijtmans, M.; Porter, N. A. J. Med. Chem. 2005, 48, 6787-6789 and refs 1-4 therein.
    • For a discussion of the importance and limitations of a-tocopherol as a biological antioxidant, see: Kim, H.-Y.; Pratt, D. A.; Seal, J. R.; Wijtmans, M.; Porter, N. A. J. Med. Chem. 2005, 48, 6787-6789 and refs 1-4 therein.
  • 7
    • 0345382641 scopus 로고    scopus 로고
    • Radical scavenging properties of flavonoids are well established: (a) McPhail, D. B.; Hartley, R. C.; Gardner, P. T.; Duthie, G. G. J. Agric. Food Chem. 2003, 51, 1684-1690.
    • Radical scavenging properties of flavonoids are well established: (a) McPhail, D. B.; Hartley, R. C.; Gardner, P. T.; Duthie, G. G. J. Agric. Food Chem. 2003, 51, 1684-1690.
  • 9
    • 33750455858 scopus 로고    scopus 로고
    • The role of flavonoids as dietary antioxidants in vivo is disputed: Lotito, S. B.; Frei, B. Free Radical Biol. Med. 2006, 41, 1727-1746.
    • The role of flavonoids as dietary antioxidants in vivo is disputed: Lotito, S. B.; Frei, B. Free Radical Biol. Med. 2006, 41, 1727-1746.
  • 11
    • 16244384516 scopus 로고    scopus 로고
    • Burkitt, M.; Jones, C.; Lawrence, A.; Wardman, P. Biochem. Soc. Symp. 2004, 71, 97-106 and refs 3-5 therein.
    • Burkitt, M.; Jones, C.; Lawrence, A.; Wardman, P. Biochem. Soc. Symp. 2004, 71, 97-106 and refs 3-5 therein.
  • 12
    • 33845451490 scopus 로고    scopus 로고
    • Recent examples of nitrones as probes and antioxidants include: (a) Xu, Y. K.; Kalyanaraman, B. Free Radical Res. 2007, 41, 1-7.
    • Recent examples of nitrones as probes and antioxidants include: (a) Xu, Y. K.; Kalyanaraman, B. Free Radical Res. 2007, 41, 1-7.
  • 24
  • 29
    • 34548534333 scopus 로고    scopus 로고
    • Preliminary investigation of such routes showed that cyclizations competed at various stages
    • Preliminary investigation of such routes showed that cyclizations competed at various stages.
  • 32
    • 0034647537 scopus 로고    scopus 로고
    • Conditions for generation of hydroxyl and methyl radicals were adapted from: Rosen, G. M.; Tsai, P.; Barth, E. D.; Dorey, G.; Casara, P.; Spedding, M.; Halpern, H. J. J. Org. Chem. 2000, 65, 4460-4463.
    • Conditions for generation of hydroxyl and methyl radicals were adapted from: Rosen, G. M.; Tsai, P.; Barth, E. D.; Dorey, G.; Casara, P.; Spedding, M.; Halpern, H. J. J. Org. Chem. 2000, 65, 4460-4463.
  • 34
    • 34548527092 scopus 로고    scopus 로고
    • 2O (1:2).
    • 2O (1:2).
  • 35
    • 34548539212 scopus 로고    scopus 로고
    • 2O (1:2).
    • 2O (1:2).
  • 36
    • 34548542822 scopus 로고    scopus 로고
    • 2O (1:2). g values referenced to strong pitch.
    • 2O (1:2). g values referenced to strong pitch.
  • 37
    • 34548532078 scopus 로고    scopus 로고
    • Hydroxyl radicals are very highly reactive, and some reaction at the phenolic position may have occurred; however, any signal for the tricyclic nitroxide 5 is initially obscured by the signal from the more abundant nitroxyl radical 12.
    • Hydroxyl radicals are very highly reactive, and some reaction at the phenolic position may have occurred; however, any signal for the tricyclic nitroxide 5 is initially obscured by the signal from the more abundant nitroxyl radical 12.
  • 39
    • 34548535111 scopus 로고    scopus 로고
    • 2O (1:2).
    • 2O (1:2).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.