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Synthesis and Anticancer Activity of New 1-Thia-4-azaspiro4.5decane Their Derived Thiazolopyrimidine and 134-Thiadiazole Thioglycosides

机译:新型1-Thia-4-azaspiro 4.5癸烷其衍生的噻唑并嘧啶和134-噻二唑硫苷的合成及抗癌活性

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摘要

New 1-thia-azaspiro[4.5]decane derivatives, their derived thiazolopyrimidine and 1,3,4-thiadiazole compounds were synthesized. The thioglycoside derivatives of the synthesized (1,3,4-thiadiazolyl)thiaazaspiro[4.5]decane and thiazolopyrimidinethione compounds were synthesized by glycosylation reactions using acetylated glycosyl bromides. The anticancer activity of synthesized compounds was studied against the cell culture of HepG-2 (human liver hepatocellular carcinoma), PC-3 (human prostate adenocarcinoma) and HCT116 (human colorectal carcinoma) cell lines and a number of compounds showed moderate to high inhibition activities.
机译:合成了新的1-硫杂氮杂[4.5]癸烷衍生物,其衍生的噻唑并嘧啶和1,3,4-噻二唑化合物。合成的(1,3,4-噻二唑基)噻唑aspiro [4.5]癸烷和噻唑并嘧啶硫酮化合物的硫代糖苷衍生物是使用乙酰化的糖基溴化物通过糖基化反应合成的。研究了合成化合物对HepG-2(人类肝脏肝细胞癌),PC-3(人类前列腺腺癌)和HCT116(人类结肠直肠癌)细胞系的细胞培养的抗癌作用,许多化合物表现出中度至高度抑制作用活动。

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