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齐墩果酸衍生酰胺的合成及其促凋亡活性

Synthesis and proapoptotic activity of oleanolic acid derived amides.

作者信息

Heller Lucie, Knorrscheidt Anja, Flemming Franziska, Wiemann Jana, Sommerwerk Sven, Pavel Ioana Z, Al-Harrasi Ahmed, Csuk René

机构信息

Martin-Luther-University Halle-Wittenberg, Organic Chemistry, Kurt-Mothes-Str. 2, D-06120 Halle (Saale), Germany.

Victor-Babes-University of Medicine and Pharmacy, Department of Pathophysiology and Department of Pharmacognosy, Eftimie Murgu Sq., 30004, 300173 Timisoara, Romania.

出版信息

Bioorg Chem. 2016 Oct;68:137-51. doi: 10.1016/j.bioorg.2016.08.004. Epub 2016 Aug 6.

Abstract

Thirty-one different 3-O-acetyl-OA derived amides have been prepared and screened for their cytotoxic activity. In the SRB assays nearly all the carboxamides displayed good cytotoxicity in the low μM range for several human tumor cell lines. Low EC50 values were obtained especially for the picolinylamides 14-16, for a N-[2-(dimethylamino)-ethyl] derivative 27 and a N-[2-(pyrrolinyl)-ethyl] carboxamide 28. These compounds were submitted to an extensive biological testing and proved compound 15 to act mainly by an arrest of the tumor cells in the S phase of the cell cycle. Cell death occurred by autophagy while compounds 27 and 28 triggered apoptosis.

摘要

已经制备了31种不同的3 - O - 乙酰基OA衍生酰胺,并对其细胞毒性活性进行了筛选。在SRB分析中,几乎所有的羧酰胺对几种人类肿瘤细胞系在低μM范围内都表现出良好的细胞毒性。特别是对于吡啶甲酰胺14 - 16、N - [2 - (二甲基氨基) - 乙基]衍生物27和N - [2 - (吡咯啉基) - 乙基]羧酰胺28,获得了低EC50值。这些化合物经过了广泛的生物学测试,证明化合物15主要通过使肿瘤细胞停滞在细胞周期的S期起作用。细胞死亡是通过自噬发生的,而化合物27和28则引发凋亡。

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