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首页> 外文期刊>Bioorganic and medicinal chemistry >Antiproliferative and apoptosis-inducing activities of alkyl gallate and gallamide derivatives related to (-)-epigallocatechin gallate.
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Antiproliferative and apoptosis-inducing activities of alkyl gallate and gallamide derivatives related to (-)-epigallocatechin gallate.

机译:没食子酸烷基酯和与(-)-表没食子儿茶素没食子酸酯有关的没食子酰胺衍生物的抗增殖和凋亡诱导活性。

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摘要

Green tea and (-)-epigallocatechin gallate (EGCG: one of the main components of green tea) are reported to have cancer-preventive activity in humans. A previous SAR study of EGCG and derivatives indicated that a galloyl group is essential for the activity. To test this hypothesis, we synthesized various alkyl gallate and gallamide derivatives and evaluated their antiproliferative effects on human leukemia HL-60 cells. Dodecyl 3,4,5-trihydroxybenzoate (6c) showed the most potent activity, being more potent than EGCG. To clarify the molecular mechanism of the antiproliferative action, we investigated the effects of 6c on various factors. Compound 6c was found to induce apoptosis mediated by endoplasmic reticulum (ER)-stress-related caspase-12. Upregulation of gadd-153, an ER-stress marker protein, was also observed. These results indicate that 6c induced apoptosis via the ER-stress-related pathway.
机译:据报道,绿茶和(-)-表没食子儿茶素没食子酸酯(EGCG:绿茶的主要成分之一)具有预防人类癌症的活性。先前对EGCG及其衍生物的SAR研究表明,没食子酰基对于该活性至关重要。为了验证该假设,我们合成了各种没食子酸烷基酯和没食子酰胺衍生物,并评估了它们对人白血病HL-60细胞的抗增殖作用。 3,4,5-三羟基苯甲酸十二烷基酯(6c)表现出最强的活性,比EGCG更有力。为了阐明抗增殖作用的分子机制,我们研究了6c对各种因素的影响。发现化合物6c诱导由内质网(ER)应激相关的caspase-12介导的凋亡。还观察到内质网应激蛋白gadd-153的上调。这些结果表明6c通过内质网应激相关途径诱导细胞凋亡。

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