首页> 外文期刊>Planta medica: Natural products and medicinal plant research >Bisbenzyltetrahydroisoquinolines, a new class of inhibitors of the mitochondrial respiratory chain complex I.
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Bisbenzyltetrahydroisoquinolines, a new class of inhibitors of the mitochondrial respiratory chain complex I.

机译:双苄基四氢异喹啉,一种新型的线粒体呼吸链复合物抑制剂。

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摘要

Four bisbenzyltetrahydroisoquinoline alkaloids (-)-medelline, (+)-antioquine, (+)-aromoline, and (+)-obamegine were isolated from the fruits of Xylopia columbiana. These compounds, the previously isolated alkaloids (+)-thaligrisine and (+)-isotetrandrine, as well as their O-acetylated derivatives were assayed on submitochondrial particles from beef heart as inhibitors of the mammalian respiratory chain. The results revealed that these alkaloids act as selective inhibitors of mitochondrial complex I in a 0.15 - 4.71 microM range. O-Acetylation, which increases their lipophilicity, considerably increased the inhibitory potency.
机译:从哥伦比亚木兰(Xylopia columbiana)的果实中分离出四个双苄基四氢异喹啉碱类生物碱(-)-美德林,(+)-antioquine,(+)-aromoline和(+)-obamegine。在来自牛心的线粒体颗粒上测定了这些化合物,先前分离的生物碱(+)-thaligrisine和(+)-异粉防己碱以及它们的O-乙酰化衍生物作为哺乳动物呼吸链的抑制剂。结果表明,这些生物碱在0.15-4.71 microM范围内充当线粒体复合体I的选择性抑制剂。 O-乙酰化增加了它们的亲脂性,大大提高了抑制能力。

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