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Design, Synthesis and Biological Evaluation of Tetrahydrodibenzo[b,g][1,8]napthyridinones as Potential Anticancer Agents and Novel Aurora Kinases Inhibitors

机译:四氢苯二醇[B,G]的设计,合成和生物学评估作为潜在的抗癌剂和新型的Aurora激酶抑制剂

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摘要

Aurora kinases inhibitors A and B have elucidated a vital role within the carcinogenesis and metastases of assorted sort of cancer. Variety of novel methodologies of drug style and support of potential enzyme inhibitors square measure listed in clinical trials, probably there‘s no advanced clinical role for kinases because the key targets for developing drug than in cancer medical care until date. Therefore, we have designed and synthesized novel tetrahydrodibenzo[b,g] [1,8] naphthyridinone molecules victimisation L-Proline in ethanol as associate adept organocatalyst for one-pot synthesis.
机译:Aurora激酶抑制剂A和B阐明了各种癌症的致癌作用和转移中的重要作用。 临床试验中列出的毒品样式和潜在酶抑制剂方形测量的各种新型方法论,可能没有激酶的先进临床作用,因为直到日期之前,都比在癌症医疗服务中开发药物的关键靶标。 因此,我们设计和合成了新型的四氢苯二酚[B,G] [1,8]萘二甲醇分子在乙醇中受害的L-丙啉盐作为一汤匙的辅助有机催化剂。

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