Balogh György T, Vukics Krisztina, Könczöl Arpád, Kis-Varga Agnes, Gere Anikó, Fischer János
Gedeon Richter Ltd, Budapest H-1475, 10. PO Box 27, Hungary.
Bioorg Med Chem Lett. 2005 Jun 15;15(12):3012-5. doi: 10.1016/j.bmcl.2005.04.043.
Synthesis of nitrone derivatives of trolox is described. Their biological evaluation was performed in vitro for scavenging different free radicals, inhibiting Fe(2+)-induced lipid peroxidation, and in vivo in a permanent middle cerebral artery occlusion model in mice. New compounds exert pharmacological activities comparable to or better than those of trolox or nitrone-type reference compounds.
本文描述了生育三烯酚(trolox)硝酮衍生物的合成。对其进行了体外清除不同自由基、抑制亚铁离子诱导的脂质过氧化的生物学评价,并在小鼠大脑中动脉永久性闭塞模型中进行了体内评价。新化合物的药理活性与生育三烯酚或硝酮类参考化合物相当或更佳。