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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Preparation of betulinic acid derivatives by chemical and biotransformation methods and determination of cytotoxicity against selected cancer cell lines
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Preparation of betulinic acid derivatives by chemical and biotransformation methods and determination of cytotoxicity against selected cancer cell lines

机译:通过化学和生物转化方法制备桦木酸衍生物,并确定其对所选癌细胞系的细胞毒性

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摘要

Several novel 2,4-dinitrophenylhydrazone betulinic acid derivatives have been prepared by chemical and biotransformation methods using fungi and carrot cells. Some compounds showed significant cytotoxicity and selectivity against some tumor cell lines. The most active, 3-[(2,4-dinitrophenyl)hydrazono]lup- (20R)-29-oxolupan-28-oic acid, showed IC50 values between 1.76 and 2.51 μM against five human cancer cell lines. The most selective, 3-hydroxy-20-[(2,4-dinitrophenyl)hydrazono]-29-norlupan-28-oic acid, was five to seven times more selective for cancer cells when compared to fibroblasts. Cell cycle analysis and apoptosis induction were studied for the most active derivatives.
机译:已经通过使用真菌和胡萝卜细胞的化学和生物转化方法制备了几种新颖的2,4-二硝基苯hydr be桦木酸衍生物。一些化合物对某些肿瘤细胞系显示出明显的细胞毒性和选择性。活性最高的3-[(2,4-二硝基苯基)肼基-lup-(20R)-29-恶唑烷-28-oic酸对五种人类癌细胞系的IC50值在1.76至2.51μM之间。与成纤维细胞相比,对癌细胞具有最高选择性的3-羟基-20-[(2,4-二硝基苯基)肼基] -29-去甲肾上腺素-28-oic酸对癌细胞的选择性高五至七倍。研究了最活跃的衍生物的细胞周期分析和凋亡诱导。

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