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Cinnamic acid derivatives as the potential modulators of prion aggregation

机译:肉桂酸衍生物作为朊病毒聚集的潜在调节剂

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摘要

Eight cinnamic acid derivatives were studied as prion inhibitors in vitro and their cytotoxicity was evaluated. Ferulic (3-methoxy-4-hydroxycinnamic) acid, 3,4,5-trimethoxycinnamic acid and methyl 3-ethoxy-4-acetamidoxycinnamate were found to inhibit amyloid fibril formation, seeding, and spontaneous aggregation of recombinant ovine prion protein. None of the compounds demonstrated cytotoxicity on human neuroblastoma SH-SY5Y cells.
机译:研究了八种肉桂酸衍生物作为体外朊病毒抑制剂,并评估其细胞毒性。 发现阿魏酸(3-甲氧基-4-羟基氨基酸)酸,3,4,5-三甲氧基氨基酸和甲基3-乙氧基-4-乙酰氨基酰胺醛酸抑制淀粉样蛋白原纤维形成,接种和自发聚集的重组绵尿朊病毒蛋白。 没有一种化合物在人神经母细胞瘤SH-SY5Y细胞上表现出细胞毒性。

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  • 来源
    《Mendeleev Communications》 |2017年第5期|共2页
  • 作者单位

    Moscow MV Lomonosov State Univ Dept Bioengn &

    Bioinformat Moscow 119991 Russia;

    Russian Acad Sci ND Zelinsky Inst Organ Chem Moscow 119991 Russia;

    Moscow MV Lomonosov State Univ Dept Bioengn &

    Bioinformat Moscow 119991 Russia;

    Moscow MV Lomonosov State Univ Dept Bioengn &

    Bioinformat Moscow 119991 Russia;

    Moscow MV Lomonosov State Univ Dept Bioengn &

    Bioinformat Moscow 119991 Russia;

    Moscow MV Lomonosov State Univ AN Belozersky Inst Physicochem Biol Moscow 119991 Russia;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
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