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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis and biological evaluation of the glycoside (25R)-3beta,16beta-diacetoxy-22-oxocholest-5-en-26-yl beta-d-glucopyranoside: a selective anticancer agent in cervicouterine cell lines.
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Synthesis and biological evaluation of the glycoside (25R)-3beta,16beta-diacetoxy-22-oxocholest-5-en-26-yl beta-d-glucopyranoside: a selective anticancer agent in cervicouterine cell lines.

机译:糖苷(25R)-3beta,16beta-diacetoxy-22-oxocholest-5-en-26-yl beta-d-glucopyranoside的合成和生物学评估:宫颈癌外侧细胞系中的一种选择性抗癌剂。

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摘要

The synthesis and biological evaluation of the new cholestane glycoside (25R)-3beta,16beta-diacetoxy-22-oxocholest-5-en-26-yl beta-d-glucopyranoside starting from diosgenin is described. This compound showed selective antiproliferative activity against CaSki, ViBo, and HeLa cervicouterine cancer cells. Its effect on the cell-cycle was determined. The cytotoxic effects of the title compound on cervicouterine cancer cell lines and human lymphocytes indicate that the main cell death process is not necrosis; hence it is not cytotoxic. The title compound induced apoptosis in cervicouterine cancer cells. Importantly, the antiproliferative activity on tumor cells did not affect the proliferative potential of peripheral blood lymphocytes. The title compound showed selective antitumor activity and greater antiproliferative activity than its aglycon, and therefore serves as a promising lead candidate for further optimization.
机译:描述了从薯in皂甙元开始合成新的胆甾烷糖苷(25R)-3beta,16beta-diacetoxy-22-oxocholest-5-en-26-yl beta-d-吡喃葡萄糖苷的合成和生物学评估。该化合物对CaSki,ViBo和HeLa宫颈外膜癌细胞具有选择性的抗增殖活性。确定了其对细胞周期的影响。标题化合物对宫颈外皮癌细胞系和人淋巴细胞的细胞毒性作用表明主要的细胞死亡过程不是坏死。因此它没有细胞毒性。该标题化合物诱导宫颈外皮癌细胞的凋亡。重要的是,对肿瘤细胞的抗增殖活性不影响外周血淋巴细胞的增殖潜能。标题化合物显示出比其糖苷配基更高的选择性抗肿瘤活性和更大的抗增殖活性,因此可作为进一步优化的有前途的候选对象。

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