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A Structurally Simplified Analogue of Geldanamycin Exhibits Neuroprotective Activity

机译:格尔德霉素的结构简化类似物表现出神经保护活性。

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The syntheses of a structurally simplified geldanamycin analogue 2 and two related compounds are described. Compound 2 conferred cytoprotection and quenched ROS and lipid peroxidation in a dose-dependent manner in Friedreichs ataxia (FRDA) lymphocytes at low micromolar concentrations. It also prevented ROS-induced damage of cellular lipid membranes and maintained the mitochondrial membrane potential of FRDA lymphocytes. In addition, 2 did not inhibit Hsp90 when tested at micromolar concentrations, exhibited no cytotoxicity, and afforded neuroprotection to differentiated SH-SY5Y cells under conditions of A-induced cell toxicity.
机译:描述了结构简化的格尔德霉素类似物2和两种相关化合物的合成。在低微摩尔浓度下,化合物2以剂量依赖性方式赋予Friedreichs共济失调(FRDA)淋巴细胞以细胞保护作用,并抑制ROS和脂质过氧化。它还可以防止ROS诱导的细胞脂质膜损伤,并保持FRDA淋巴细胞的线粒体膜电位。另外,当以微摩尔浓度测试时,2没有抑制Hsp90,没有细胞毒性,并且在A诱导的细胞毒性条件下对分化的SH-SY5Y细胞提供了神经保护。

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