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A novel ROCK inhibitor: off-target effects of metformin

机译:一种新型岩石抑制剂:二甲双胍的脱靶效果

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In drug discovery, most small molecules cannot cross many stages, only a few can become drug candidates. Once the drug molecule is approved and marketed, nontarget effects that are not easily distinguishable from the actual target of the drugs might be evaluated. This situation restricts the treatment. Thus, the discovery of new drugs is a very long and expensive process. In recent years, without developing new drugs, the approach of using different and new target molecules in new indications apart from the indications of licensed drug molecules has gained importance. In this study, using the connectivity map program, it was determined that metformin and tolbutamide used in the treatment of type II diabetes had the potential to inhibit Rho kinase. In the experimental results to confirm this data, it has been shown that metformin and tolbutamide decrease the cell area within 24 h and metformin inhibits the activation of Rho kinase in MCF-7 cells. These results indicate that metformin, which is used in the treatment of type II diabetes, acts as a ROCK inhibitor. Metformin has potential in the treatment of various pathological conditions in which Rho kinase has a role.
机译:在药物发现中,大多数小分子不能跨越许多阶段,只有少数可以成为毒品候选人。一旦药物分子被批准和销售,就可以评估从药物的实际目标不容易区分的非明显效应。这种情况限制了治疗。因此,新药的发现是一个非常漫长而昂贵的过程。近年来,在不开发新药的情况下,除了许可药物分子的适应症之外,在新的适应症中使用不同和新的目标分子的方法已经获得了重要性。在本研究中,使用连接图程序,确定用于治疗II型糖尿病的二甲双胍和甲丁酰胺具有抑制Rho激酶的可能性。在实验结果确定该数据的实验结果中,已经表明,二甲双胍和甲醛酰胺在24小时内降低细胞面积,并且二甲双胍抑制MCF-7细胞中rhO激酶的激活。这些结果表明,二甲双胍用于治疗II型糖尿病,其作用为岩石抑制剂。二甲双胍具有治疗各种病理条件的潜力,其中Rho激酶具有作用。

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