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Molecular basis of scavenging effect of zonisamide on hydroxyl radical <i>in vitro</i>
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作者 Ken-ichi Tanaka takeshi nanba +3 位作者 Tomoyuki Furubayashi Yasuko Noda Luther James Willmore Akitane Mori 《Journal of Biophysical Chemistry》 2012年第3期256-258,共3页
Zonisamide (ZNS), a commonly used anticonvulsant, scavenged hydroxyl radicals at a clinically relevant concentration. Reactants of ZNS with hydrogen peroxide and with hydrogen peroxide plus UV irradiation, yielding hy... Zonisamide (ZNS), a commonly used anticonvulsant, scavenged hydroxyl radicals at a clinically relevant concentration. Reactants of ZNS with hydrogen peroxide and with hydrogen peroxide plus UV irradiation, yielding hydroxyl radicals, were analyzed by the LC/MS technique. Many small fragments were found in the both reactions, suggesting that ZNS was decomposed not only by hydroxyl radicals but also by hydrogen peroxide. Furthermore, mass-fragment-grams showed that m/z: 213 (ZNS itself) was decreased markedly and m/z: 118 (may be a decomposed product by ring cleavage of ZNS) was detected specifically by treatment with hydroxyl radical. These data suggested that ZNS may react directly with free radicals. 展开更多
关键词 ZONISAMIDE HYDROXYL RADICALS LC/MS ESR
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