Literature DB >> 17336073

Free radical trapping properties of several ethyl-substituted derivatives of 5-ethoxycarbonyl-5-methyl-1-pyrroline N-oxide (EMPO).

Klaus Stolze1, Natascha Rohr-Udilova, Thomas Rosenau, Andreas Hofinger, Hans Nohl.   

Abstract

The spin trapping behavior of several ethyl-substituted EMPO derivatives, cis- and trans-5-ethoxycarbonyl-3-ethyl-5-methyl-pyrroline N-oxide (3,5-EEMPO), 5-ethoxycarbonyl-4-ethyl-5-methyl-pyrroline N-oxide (4,5-EEMPO), cis- and trans-5-ethoxycarbonyl-5-ethyl-3-methyl-pyrroline N-oxide (5,3-EEMPO), and 5-ethoxycarbonyl-5-ethyl-4-methyl-pyrroline N-oxide (5,4-EEMPO), toward a series of different oxygen- and carbon-centered radicals, is described. Considerably different stabilities of the superoxide adducts (ranging from about 12 to 55 min) as well as the formation of other radical adducts were observed.

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Year:  2007        PMID: 17336073     DOI: 10.1016/j.bmc.2007.02.025

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  1 in total

1.  Fused-ring derivatives of quinoxalines: spectroscopic characterization and photoinduced processes investigated by EPR spin trapping technique.

Authors:  Zuzana Barbieriková; Dana Dvoranová; Maroš Bella; Viktor Milata; Adriana Czímerová; Vlasta Brezová
Journal:  Molecules       Date:  2014-08-12       Impact factor: 4.411

  1 in total

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