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首页> 外文期刊>Journal of Medicinal Chemistry >Discovery of Novel Polo-Like Kinase 1 Polo-Box Domain Inhibitors to Induce Mitotic Arrest in Tumor Cells
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Discovery of Novel Polo-Like Kinase 1 Polo-Box Domain Inhibitors to Induce Mitotic Arrest in Tumor Cells

机译:发现新型Polo样激酶1 Polo框域抑制剂诱导肿瘤细胞中的有丝分裂被逮捕。

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摘要

Polo-like kinase 1(Plk1) is vital for cell mitosis and has been identified as anticancer target. Its polo-box domain (PBD) mediates substrate binding, blocking of which may offer selective Plk1 inhibition compared to kinase domain inhibitors. Although several PBD inhibitors were reported, most of them suffer from low cell activity. Here, we report the discovery of novel inhibitors to induce mitotic arrest in HeLa cells by virtual screening with Plk1 PBD and cellular activity testing. Of the 81 compounds tested in the cell assay, 10 molecules with diverse chemical scaffolds are potent to induce mitotic arrest of HeLa at low micromolar concentrations. The best compound induces mitotic arrest of HeLa cells with an EC50 of 4.4 mu M. The cellular active inhibitors showed binding to Plk1 PBD and compete with PBD substrate in microscale thermophoresis analysis.
机译:Polo样激酶1(Plk1)对细胞有丝分裂至关重要,已被确定为抗癌靶标。它的polo-box域(PBD)介导底物结合,与激酶域抑制剂相比,阻断底物可能提供选择性的Plk1抑制。尽管已报道了几种PBD抑制剂,但其中大多数都具有细胞活性低的缺点。在这里,我们报道了通过用Plk1 PBD虚拟筛选和细胞活性测试在HeLa细胞中诱导有丝分裂停滞的新型抑制剂的发现。在细胞试验中测试的81种化合物中,有10种具有不同化学支架的分子有效地诱导了低微摩尔浓度的HeLa的有丝分裂停滞。最佳化合物可诱导HeLa细胞的有丝分裂停滞,EC50为4.4μM。在微尺度热泳分析中,细胞活性抑制剂显示与Plk1 PBD结合并与PBD底物竞争。

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