国家自然科学基金重点项目(20032020)和广东省自然科学基金(2KM04103S)资助项目.
This work was supported by grants from The National Natural Sciences Foundation of China (20032020) and The National Natural Sciences Foundation of Guangdong (2KM04103S).
合成了一系列3-羟基-4(1H)-吡啶酮类衍生物,并研究了它们对5-脂氧合酶的抑制作用. 发现6-取代-3-羟基-4(1H)-吡啶酮化合物(2a~2e)对5-脂氧合酶具有显著抑制作用, 特别是6-苯硫基-1-苯基-2-甲基-3-羟基-4(1H)-吡啶酮(2a)的抑制效果最好(IC50=2.52 μmol/L). 6-位没有取代基的羟基吡啶酮类化合物对5-脂氧合酶却没有抑制作用. 讨论了6-取代-3-羟基-4(1H)-吡啶酮类化合物对5-脂氧合酶的抑制作用机制.
A series of pyridinone derivatives were synthesized and examined for inhibition of 5-lipoxgenase. The 6-substituted pyridinone derivatives(2a~2e) exhibited a prominent inhibitory activity on 5-lipoxygenase. Among them, 6-phenylthio-1-phenyl-2-methyl-3-hydroxy-4(1H)-pyridinone (2a) showed the most potent inhibitory activity (IC50=2.52 μmol/L). As removal of substituent at 6- position of pyridinones, the inhibitory abilities of these compounds were almost vanished. The inhibition mechanism of pyridinone derivatives was discussed.
谢文林,马林,郭刚军,段志芳,邹兰,古练权,王骏.吡啶酮类衍生物对5-脂氧合酶的抑制作用[J].生物化学与生物物理进展,2002,29(4):588-591
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