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Synthesis and biological assessment of novel acylhydrazone derivatives of 2-methyl-1,4-naphthoquinone

机译:2-甲基-1,4-萘醌新型酰基hydr衍生物的合成及生物学评价

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Naphthoquinones are medicinally important molecules with a diverse array of biological properties such as antimicrobial, antifungal, antiviral, anti-inflammatory, anti-artherosclerotic and anticarcinogenic activities. In this study, we report the simple and direct preparation of a new group of novel menadione-hydrazone conjugates by reaction of 2-methyl-1,4-naphthoquinones with several aliphatic, aromatic and nucleobase hydrazides. The menadione-hydrazone conjugates were produced in excellent yields and characterized by IR, NMR and HRMS. The menadione derivatives were tested for their anticancer effects against human colon cancer HCT116 and human breast cancer MCF-7 cell lines. Interestingly, the molecules displayed disparate activities against both cell lines; the menadione hydrazones derived from the lipophilic myristic hydrazide and stearic hydrazide exhibited the most potent activity against HCT116 cell lines with IC50 of 89 and 64 μM. The most effective compounds against MCF-7 cells were the lauric hydrazide and benzoic hydrazide-derived menadione hydrazones with IC50 of 56 μM.
机译:萘醌是具有多种生物学特性的重要医学分子,例如抗微生物,抗真菌,抗病毒,抗炎,抗动脉粥样硬化和抗癌活性。在这项研究中,我们报告了通过2-甲基-1,4-萘醌与几种脂肪族,芳香族和核碱基酰肼的反应,简单而直接地制备了一组新的新甲萘醌-hydr共轭物。甲萘醌-hydr共轭物的产率高,并通过IR,NMR和HRMS表征。测试了甲萘醌衍生物对人结肠癌HCT116和人乳腺癌MCF-7细胞系的抗癌作用。有趣的是,这些分子对两种细胞系均表现出不同的活性。源自亲脂性肉豆蔻酰肼和硬脂酰肼的甲萘醌表现出对HCT116细胞系最有效的活性,IC50为89和64μM。对MCF-7细胞最有效的化合物是月桂酰肼和苯甲酰肼衍生的甲萘醌,IC50为56μM。

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