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Targeting GLI proteins in human cancer by small molecules (WO2014116651 A1): a patent evaluation

机译:通过小分子靶向人类癌症中的GLI蛋白(WO2014116651 A1):一项专利评估

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摘要

The invention reviewed in this patent evaluation is the synthesis and application of small molecule inhibitors of Gli transcriptional activity as potential anticancer agents. The oncogenic nature of Gli proteins has been traditionally associated with the hedgehog (Hh) signaling pathway; however, the recent identification of aberrant Gli activation unrelated to Hh signaling has prompted drug discovery efforts directly targeting Gli proteins. The central core of the compounds described in this patent (WO2014116651 A1) is structurally analogous to the pyrazoline scaffold previously disclosed by these inventors. Data describing the inhibitory activity of these compounds against the Hh pathway in vitro and in Hh-dependent in vivo models of human cancer are not provided. For this patent disclosure, the inventors primarily focus on the anticancer properties of their compounds in lung and lung-related malignancies. The compounds are moderately active in these models, but they do not exhibit the overall preclinical profile generally required for advancement into clinical trials.
机译:该专利评估中审查的发明是作为潜在抗癌剂的Gli转录活性小分子抑制剂的合成和应用。传统上,Gli蛋白的致癌性与刺猬(Hh)信号传导通路相关;但是,最近鉴定出与Hh信号传导无关的异常Gli激活,促使药物发现工作直接针对Gli蛋白。该专利(WO2014116651 A1)中描述的化合物的中心核心在结构上类似于这些发明人先前公开的吡唑啉支架。没有提供描述这些化合物在体外和在人类癌症的Hh依赖性体内模型中对Hh途径的抑制活性的数据。对于该专利公开,发明人主要关注其化合物在肺和与肺相关的恶性肿瘤中的抗癌特性。这些化合物在这些模型中具有中等活性,但它们并未展现出进入临床试验所需的总体临床前概况。

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