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Imparting aromaticity to 2-pyridone derivatives by O-alkylation resulted in new competitive and non-competitive PIM-1 kinase inhibitors with caspase-activated apoptosis
Journal of Enzyme inhibition and Medicinal Chemistry ( IF 5.6 ) Pub Date : 2024-01-17 , DOI: 10.1080/14756366.2024.2304044
Marwa E. Abdelaziz 1 , Mostafa M. M. El-Miligy 1 , Salwa M. Fahmy 1 , Marwa M. Abu-Serie 2 , Aly A. Hazzaa 1 , Mona A. Mahran 1
Affiliation  

New aromatic O-alkyl pyridine derivatives were designed and synthesised as Proviral Integration Moloney (PIM)-1 kinase inhibitors. 4c and 4f showed potent in vitro anticancer activity against NFS-6...

中文翻译:

通过 O-烷基化赋予 2-吡啶酮衍生物芳香性,产生具有 caspase 激活细胞凋亡的新型竞争性和非竞争性 PIM-1 激酶抑制剂

设计并合成了新的芳香族 O-烷基吡啶衍生物作为前病毒整合莫洛尼 (PIM)-1 激酶抑制剂。4c 和 4f 显示出针对 NFS-6 的有效体外抗癌活性...
更新日期:2024-01-17
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