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• W2014332703 abstract "Six novel H2O-soluble β-cyclodextrin derivatives containing a 1,2-benzisoselenazol-3(2H)-one moiety were synthesized by a convenient method in 25–60% yield and characterized by MS, elemental analysis, IR, 1H-NMR, and UV/VIS spectroscopy. The conformations of these β-cyclodextrin derivatives 1–6 were analyzed by circular dichroism and fluorescence-lifetime experiments. The superoxide dismutase (SOD) activities of 1–6 were determined by auto-oxidation of pyrogallol at 25.0° in buffer solution (pH 8.2), giving relatively high SOD activities of up to 121–330 U/mg. Also, the glutathione peroxidase (GPX) activities of hosts 1–6, determined by the method of Wilson at 37° in buffer solution (pH 7.0), show good GPX activities in the range of 0.34–0.86 U/μmol. The mimicking results of the bifunctional artificial enzyme models 1–6 were globally compared with regard to their structural and conformational difference." @default.
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• W2014332703 date "2002-01-01" @default.
• W2014332703 modified "2023-10-11" @default.
• W2014332703 title "Synthesis of Organoselenium-Modifiedβ-Cyclodextrins Possessing a 1,2-Benzisoselenazol-3(2H)-one Moiety and Their Enzyme-Mimic Study" @default.
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• W2014332703 doi "https://doi.org/10.1002/1522-2675(200201)85:1<9::aid-hlca9>3.0.co;2-h" @default.
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