首页> 美国卫生研究院文献>Biochemical Journal >Radical adducts of nitrosobenzene and 2-methyl-2-nitrosopropane with 1213-epoxylinoleic acid radical 1213-epoxylinolenic acid radical and 1415-epoxyarachidonic acid radical. Identification by h.p.l.c.-e.p.r. and liquid chromatography-thermospray-m.s.
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Radical adducts of nitrosobenzene and 2-methyl-2-nitrosopropane with 1213-epoxylinoleic acid radical 1213-epoxylinolenic acid radical and 1415-epoxyarachidonic acid radical. Identification by h.p.l.c.-e.p.r. and liquid chromatography-thermospray-m.s.

机译:亚硝基苯和2-甲基-2-亚硝基丙烷与1213-环氧亚油酸基1213-环氧亚麻酸基和1415-环氧花生四烯酸基的自由基加合物。通过h.p.l.c.-e.p.r.和液相色谱-热喷涂-m.s。

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摘要

Linoleic acid-derived radicals, which are formed in the reaction of linoleic acid with soybean lipoxygenase, were trapped with nitrosobenzene and the resulting radical adducts were analysed by h.p.l.c.-e.p.r. and liquid chromatography-thermospray-m.s. Three nitrosobenzene radical adducts (peaks I, II and III) were detected; these gave the following parent ion masses: 402 for peak I, 402 for peak II, and 386 for peak III. The masses of peaks I and II correspond to the linoleic acid radicals with one more oxygen atom [L(O).]. The radicals are probably carbon-centred, because the use of 17O2 did not result in an additional hyperfine splitting. Computer simulation of the peak I radical adduct e.p.r. spectrum also suggested that the radical is carbon-centred. The peak I radical was also detected in the reaction of 13-hydroperoxylinoleic acid with FeSO4. From the above results, peak I is probably the 12,13-epoxylinoleic acid radical. An h.p.l.c.-e.p.r. experiment using [9,10,12,13-2H4]linoleic acid suggested that the 12,13-epoxylinoleic acid radical is a C-9-centred radical. Peak II is possibly an isomer of peak I. Peak III, which was observed in the reaction mixture without soybean lipoxygenase, corresponds to a linoleic acid radical (L.). The 12,13-epoxylinoleic acid radical, 12,13-epoxylinolenic acid radical and 14,15-epoxyarachidonic acid radical were also detected in the reactions of linoleic acid, linolenic acid and arachidonic acid respectively, with soybean lipoxygenase using nitrosobenzene and 2-methyl-2-nitrosopropane as spin-trapping agents.
机译:在亚油酸与大豆脂氧合酶反应中形成的亚油酸衍生基团被亚硝基苯捕获,并通过h.p.l.c.-e.p.r分析所得的自由基加合物。和液相色谱-热喷涂-m.s。检测到三个亚硝基苯自由基加合物(峰I,II和III);这些给出了以下母离子质量:峰I为402,峰II为402,峰III为386。峰I和峰II的质量对应于具有一个以上氧原子[L(O)]的亚油酸基团。这些自由基可能是以碳为中心的,因为使用17O2不会导致额外的超细分裂。峰I自由基加合物e.p.r.的计算机模拟光谱还表明该自由基以碳为中心。在13-氢过氧亚油酸与FeSO4的反应中也检测到峰I自由基。根据以上结果,峰I可能是12,13-环氧亚油酸基团。 h.p.l.c.-e.p.r. [9,10,12,13-2H4]亚油酸的实验表明,12,13-环氧亚油酸基团是一个C-9中心的基团。峰II可能是峰I的异构体。在没有大豆脂氧合酶的反应混合物中观察到峰III,其对应于亚油酸自由基(L.)。在亚油酸,亚麻酸和花生四烯酸与大豆脂加氧酶的反应中,分别用亚硝基苯和2-甲基亚砜检测到了12,13-环氧亚油酸自由基,12,13-环氧亚油酸自由基和14,15-环氧花生四烯酸自由基。 -2-亚硝基丙烷作为自旋捕集剂。

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