Pim激酶抑制剂和基于嘧啶的抗癌药物

Ibrahim Issa, A. Hammam, Helmy M. Sakr, RezkRezk A. Ayyad
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引用次数: 0

摘要

人磷脂酰肌醇甘露糖激酶(Pim激酶)是发现新的抗癌药物的重要生物学靶点。此外,嘧啶类化合物是许多抗癌药物的重要组成部分。因此,对Pim激酶抑制剂和基于嘧啶的抗癌药物进行了文献综述。在这项调查中,我们介绍了临床评估的Pim激酶抑制剂,包括咪唑[1,2-b]吡嗪类、异硫汀类、噻唑烷-2,4-二酮类、吡啶胺类和二氨基吡唑类。此外,还介绍了正在开发的Pim激酶抑制剂。这些化合物包括吡啶-喹啉、苯并咪唑-吲哚、氰基吡啶、吡啶噻吩[3,2-d]吡啶-4-酮、恶二唑和3,4-二氢吡咯[1,2-a]吡嗪-1(2h)-酮。此外,还讨论了不同的嘧啶类抗癌药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PIM KINASES INHIBITORS AND PYRIMIDINE-BASED ANTICANCER AGENTS
Human phosphatidyl inositol mannoside kinases (Pim kinases) are important biological target for discovery of new anticancer agents. In addition, Pyrimidines have a good contribution as building blocks of many anticancer agents. Hence, a literature survey about Pim kinases inhibitors and pyrimidine-based anticancer agents have been achieved. In this survey, we introduced Pim kinase inhibitors under clinical assessment including imidazo[1,2-b ]pyridazines, isatins, thiazolidine-2,4-diones, pyridinamines, and diaminopyrazoles. In addition, Pim kinase inhibitors under development were presented. These compounds include pyridine-quinolines, benzimidazoles indoles, cyano pyridines, pyridothieno[3,2-d ]pyrimidin-4-ones, oxadiazole, and 3,4-dihydropyrrolo[1,2-a]pyrazin-1(2 H )-ones. Furthermore, different pyrimidine-based anticancer agents have been discussed.
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