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Structural optimization of indole based compounds for highly promising anti-cancer activities: Structure activity relationship studies and identification of lead molecules

机译:基于吲哚基化合物的结构优化,用于高前远抗癌活动:结构活动关系研究与铅分子的鉴定

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摘要

Based on the anti-cancer data of previous compounds, 27 more compounds were synthesized and subjected to anti-cancer screening. Compounds were tested over 60 human tumor cell lines of different types of cancer. As per the data available, some compounds exhibited appreciable anti-cancer properties over certain cell lines with their GI50 in nM range. With the help of UV-vis spectral studies, enzyme immunoassay and molecular modeling studies, dihydrofolate reductase was found to be the probable cellular target of the compounds under present investigation.
机译:基于先前化合物的抗癌数据,合成27种化合物并进行抗癌筛选。 在不同类型的癌症的60例人肿瘤细胞系上测试化合物。 根据可用的数据,一些化合物在某些细胞系中表现出可观的抗癌性质,其GI50在NM范围内。 借助于紫外 - 可见的光谱研究,酶免疫测定和分子建模研究,发现二氢氢醇还原酶是本前研究的化合物的可能细胞靶标。

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