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首页> 外文期刊>ACS Omega >Synthesis and Neuroprotective Properties of N-Substituted C-Dialkoxyphosphorylated Nitrones
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Synthesis and Neuroprotective Properties of N-Substituted C-Dialkoxyphosphorylated Nitrones

机译:N-取代的C-二烷氧基磷酸化硝基的合成及神经保护作用

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Herein, we report the synthesis and neuroprotective power of some N-substituted C-(dialkoxy)phosphorylated nitrones 4a–g, by studying their ability to increase the cell viability, as well as their capacity to reduce necrosis and apoptosis. We have identified (Z)-N-tert-butyl-1-(diethoxyphosphoryl)methanimine oxide (4e) as the most potent, nontoxic, and neuroprotective agent, with a high activity against neuronal necrotic cell death, a result that correlates very well with its great capacity for the inhibition of the superoxide production (72%), as well as with the inhibition of lipid peroxidation (62%), and the 5-lipoxygenase activity (45%) at 100 μM concentrations. Thus, nitrone 4e could be a convenient promising compound for further investigation.
机译:在这里,我们通过研究N-取代的C-(二烷氧基)磷酸化的硝酮4a-g的合成和神经保护作用,研究了它们增加细胞活力的能力以及减少坏死和凋亡的能力。我们已经确定(Z)-N-叔丁基-1-(二乙氧基磷酰基)甲亚胺氧化物(4e)是最有效,无毒和神经保护剂,对神经元坏死细胞死亡具有很高的活性,其相关性非常好其在100μM浓度下具有抑制超氧化物产生的强大能力(72%),对脂质过氧化的抑制作用(62%)和5-脂氧合酶活性(45%)。因此,硝酮4e可能是方便的有希望的化合物,用于进一步研究。

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