Synthesis and anticancer activity of 5-sulfonyl derivatives of 1,3-oxazole-4-carboxylates

S. Pilyo, Оlexandr Kozachenko, V. Zhirnov, M. Kachaeva, O. Kobzar, A. Vovk, V. Brovarets
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引用次数: 2

Abstract

A series of new 2-aryl 5-sulfonyl-1,3-oxazole-4-carboxylates for NCI anticancer screening protocol against 60 cancer cell lines were synthesized. Screening was performed in vitro on 60 cell lines of lungs, kidneys, CNS, ovaries, prostate, and breast cancer, leukemia, and melanoma. Methyl 5-benzylsulfonyl-2-phenyl-1,3-oxazole-4-carboxylate 15 exhibited potent and broad range of cytotoxic activity against tested human cancer cells with average GI50, TGI, and LC50 values of 5.37·10-6, 1.29·10-5 and 3.6·10-5 mol/L respectively. Molecular docking was used to evaluate the possible interaction of compound 15 with tubulin as well as a complex formation with CDK2.
1,3-恶唑-4-羧酸酯5-磺酰基衍生物的合成及其抗癌活性
合成了一系列新的2-芳基5-磺酰-1,3-恶唑-4-羧酸盐,用于60种癌细胞的NCI抗癌筛选方案。对肺、肾、中枢神经系统、卵巢、前列腺、乳腺癌、白血病和黑色素瘤等60种细胞系进行体外筛选。5-苄基磺酰基-2-苯基-1,3-恶唑-4-羧酸甲酯15对人癌细胞具有广泛的细胞毒活性,其平均GI50、TGI和LC50分别为5.37·10-6、1.29·10-5和3.6·10-5 mol/L。分子对接用于评估化合物15与微管蛋白可能的相互作用以及与CDK2形成复合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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