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首页> 外文期刊>Archiv der Pharmazie >Synthesis and Evaluation of New Dithiocarbamic Acid 6,11-Dioxo-6,11-dihydro-1H-anthra[1,2-d]-imidazol-2-yl Methyl Esters
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Synthesis and Evaluation of New Dithiocarbamic Acid 6,11-Dioxo-6,11-dihydro-1H-anthra[1,2-d]-imidazol-2-yl Methyl Esters

机译:新型二硫代氨基甲酸6,11-二氧-6,11-二氢-1H-蒽[1,2-d]-咪唑-2-基甲基酯的合成与评价

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摘要

A novel series of dithiocarbamic acid 6,11-dioxo-6,11-dihydro-1H-anthra[1,2-d]imidazol-2-yl methyl esters were synthesized and their cytotoxic and apoptotic activities were evaluated on HeLa cells. Some of these compounds showed potent cytotoxic activities and are able to induce the apoptosis mechanism in this cell line. Especially, 2c, 2d, and 2f had a high cytotoxic activity with an IC50 value of 8 or 10M at 24h. These three compounds also induced HeLa cell apoptosis as compared to mitoxantrone. Particularly, 3M of 2f induced a high rate of early apoptotic cells (12.9%) at 6h whereas mitoxantrone induced early apoptosis (5.5%) at 24h. Compound 2c demonstrated a high ADP/ATP ratio (9.31) in HeLa cells at 12h compared to mitoxantrone or other compounds, suggesting that 2c might induce HeLa cell apoptosis through the mitochondrial pathway. Caspase-3 activity started to increase after treatment with 6M of 2c for 6h, and the maximal peak of activity was obtained at 12h of incubation time. All three compounds were found to be potent apoptotic inducers compared to mitoxantrone.
机译:合成了一系列新的二硫代氨基甲酸6,11-二氧代-6,11-二氢-1H-蒽[1,2-d]咪唑-2-基甲基酯,并对其在HeLa细胞上的细胞毒性和凋亡活性进行了评估。这些化合物中的一些显示出有效的细胞毒性活性,并能够诱导该细胞系的凋亡机制。特别是2c,2d和2f具有高的细胞毒活性,在24h时的IC50值为8或10M。与米托蒽醌相比,这三种化合物还诱导HeLa细胞凋亡。特别地,3f的2f在6h诱导高比率的早期凋亡细胞(12.9%),而米托蒽醌在24h诱导早期凋亡(5.5%)。与米托蒽醌或其他化合物相比,化合物2c在12h时在HeLa细胞中显示出较高的ADP / ATP比(9.31),表明2c可能通过线粒体途径诱导HeLa细胞凋亡。用6M 2c处理6h后,Caspase-3活性开始增加,并且在孵育时间12h达到最大活性峰。与米托蒽醌相比,发现这三种化合物都是有效的凋亡诱导剂。

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