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Synthesis characterization and antineoplastic activity of bis-aziridinyl dimeric naphthoquinone - a novel class of compounds with potent activity against acute myeloid leukemia cells

机译:双氮丙啶基二聚萘醌的合成表征和抗肿瘤活性-一种新型的对急性髓性白血病细胞具有有效活性的化合物

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摘要

The synthesis, characterization and antileukemic activity of rationally designed amino dimeric naphthoquinone (BiQ) possessing aziridine as alkylating moiety is described. Bis-aziridinyl BiQ decreased proliferation of acute myeloid leukemia (AML) cell lines and primary cells from patients, and exhibited potent (nanomolar) inhibition of colony formation and overall cell survival in AML cells. Effective production of reactive oxygen species (ROS) and double stranded DNA breaks (DSB) induced by bis-aziridinyl BiQ is reported. Bis-dimethylamine BiQ, as the isostere of bis-aziridinyl BiQ but without the alkylating moiety did not show as potent anti-AML activity. Systemic administration of bis-aziridinyl BiQ was well tolerated in NSG mice.
机译:描述了以氮丙啶为烷基化部分的合理设计的氨基二聚萘醌(BiQ)的合成,表征和抗白血病活性。 Bis-aziridinyl BiQ可以降低患者的急性髓细胞白血病(AML)细胞系和原代细胞的增殖,并在AML细胞中表现出有效的(纳摩尔)抑制集落形成和总体细胞存活率。据报道,由双叠氮基吡啶基BiQ可以有效产生活性氧(ROS)和双链DNA断裂(DSB)。双二甲胺BiQ,作为双叠氮烷基BiQ的等排物,但没有烷基化部分,没有显示出有效的抗AML活性。在NSG小鼠中对双氮丙啶基BiQ的全身给药耐受性良好。

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