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Discovery of Aminoquinolines as a New Class of Potent Inhibitors of Heat Shock Protein 90 (Hsp90): Synthesis Biology and Molecular Modeling

机译:氨基喹啉类作为热休克蛋白90(Hsp90)的新型强抑制剂的发现:合成生物学和分子建模。

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摘要

The molecular chaperone Hsp90 plays important roles in maintaining the malignant phenotypes. Recent studies suggest that Hsp90 exerts high affinity interactions with multiple oncoproteins, which are essential for the growth of tumor cells. As a result, research has been focused on finding Hsp90 probes as potential and selective anticancer agents. In a high-throughput screening exercise, we identified quinoline >7 as a moderate inhibitor of Hsp90. Further hit identification, SAR studies and biological investigation revealed several synthetic analogs in this series with micromolar activities in both fluorescent polarization (FP) assay and a cell-based western-blot (WB) assay. These compounds represent a new class of Hsp90 inhibitors with simple chemical structures.
机译:分子伴侣Hsp90在维持恶性表型中起重要作用。最近的研究表明,Hsp90与多种癌蛋白具有高亲和力相互作用,这对于肿瘤细胞的生长至关重要。结果,研究集中在发现Hsp90探针作为潜在的和选择性的抗癌剂上。在高通量筛选研究中,我们确定了喹啉> 7 为Hsp90的中度抑制剂。进一步的命中鉴定,SAR研究和生物学研究揭示了该系列中的几种合成类似物,在荧光偏振(FP)分析和基于细胞的Western-blot(WB)分析中均具有微摩尔活性。这些化合物代表了一类具有简单化学结构的Hsp90抑制剂。

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