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Design and synthesis of naphthoquinone derivatives as antiproliferative agents and 20S proteasome inhibitors

机译:萘醌衍生物作为抗增殖剂和20S蛋白酶体抑制剂的设计与合成

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摘要

Fourteen naphthoquinone derivatives (1-14) were designed based on a putative proteasome inhibitor PI-083. These compounds were synthesized and evaluated against A549, DU145, KB, and KBvin tumor cell lines. Six compounds (2, 4, 8, 9, 10, and 13) showed antiproliferative activities comparable to that of PI-083. Among them, compound 8 was confirmed as a 20S proteasome inhibitor in both in vitro and cell-based assays. These findings endorse further optimization efforts based on this structural phenotype to develop potential anticancer drug candidates.
机译:基于假定的蛋白酶体抑制剂PI-083设计了十四种萘醌衍生物(1-14)。合成这些化合物并针对A549,DU145,KB和KBvin肿瘤细胞系进行评估。六个化合物(2、4、8、9、10和13)显示出与PI-083相当的抗增殖活性。其中,化合物8在体外和基于细胞的测定中均被确认为20S蛋白酶体抑制剂。这些发现支持基于这种结构表型的进一步优化工作,以开发潜在的抗癌药物候选物。

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