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Synthesis of N-Methylpiperidin-4-one Derivatives and Evaluation of Their Anti-Endometrial Cancer Activity

机译:N-甲基哌啶-4-一种衍生物的合成及其抗子宫内膜癌活性的评价

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摘要

Four novel N-methylpiperidin-4-one derivatives were synthesized and characterized by IR, H-1 NMR, HRMS, and single crystal X-ray crystallography. The anticancer activity of these compounds was studied on five human endometrial cancer cell lines (RL-95-2, HEC-1A, HEC-1B, AN3CN and HECCL-1). Efficient antitumor effect was found for the 3,5-difluorophenyl-and 3-cyanophenyl-substituted derivatives.
机译:通过IR,H-1NMR,HRMS和单晶X射线晶体学合成了四种新的N-甲基哌啶-4-一种衍生物。 研究了这些化合物的抗癌活性在五个人子宫内膜癌细胞系(RL-95-2,HEC-1A,HEC-1B,AN3CN和HECCL-1)上进行了研究。 发现了3,5-二氟苯基和3-氰基苯基取代的衍生物的有效抗肿瘤效应。

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