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Anticancer Activity and DNA Binding Studies of Novel 3,7-Disubstituted Benzopyrones

机译:新型3,7脱生的苯并酮的抗癌活性和DNA结合研究

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摘要

We have designed and synthesized novel 7-substituted-3- acetyl-benzopyrones 9a-9g and ethyl 7-substituted-3-carboxylate- benzopyrones 10a-10d and screened for anticancer activity using MTT assay. Most of the tested compounds have shown very good activity against A549 cell line (lung cancer cell-line) and MCF7 cell line (breast cancer cell-line) compared to 5-Fluorouracil. Compound 9b and 9e exhibited excellent anticancer activity with IC-(50) 0.16 nM against A549 cell line and 84.8 nM against MCF7 cell line respectively. Compounds 9b and 9e showed excellent anticancer activity at very low concentration, well falling in nanomolar region. Compounds 9b and 9e exhibited very good binding constant for DNA binding through intercalation in UV based DNA titration which was further confirmed by fluorescence based EtBr displacement assay in DNA-EtBr complex.
机译:我们已经设计和合成了新型的7-取代-3-acetyl-Benzopyrones 9a-9g和7-溶解的3-羧酸苯甲酸苯甲酸苯甲酸苯甲酸苯甲酸苯胺苯酚 - 苯并甲酮10A-10D,并使用MTT分析筛选抗癌活性。 与5-氟尿嘧啶相比,大多数测试化合物对A549细胞系(肺癌细胞系)和MCF7细胞系(乳腺癌细胞系)的活性非常好。 化合物9b和9e分别针对A549细胞系具有出色的抗癌活性,分别针对A549细胞系和84.8 nm对MCF7细胞系。 化合物9b和9e在非常低的浓度下显示出极好的抗癌活性,在纳摩尔区域井下。 化合物9b和9e通过基于紫外线的DNA滴定在DNA-ETBR基于DNA-ETBR复合物中的基于荧光的ETBR位移测定法进一步证实了DNA结合的结合常数。

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