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The cytotoxic activities of cardiac glycosides from Streptocaulon juventas and the structure-activity relationships

机译:尤文链霉菌强心苷的细胞毒活性及其构效关系

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摘要

A series of cardiac glycosides were isolated and identified from the anti-tumor fraction of the root of Streptocaulon juventas in previous studies. In the present research, the cytotoxic activities of the 43 cardiac glycosides on three cell lines, human lung A549 adenocarcinoma cell, large cell lung cancer NCI-H460 cell and normal human fetal lung fibroblast MRC-5 cell, were evaluated in vitro. Most of the tested compounds showed potent inhibitory activities toward the three cell lines. Then, the structure-activity relationships were discussed in detail. It was indicated that hydroxyl and acetyl groups at C-16 increased the activity, whereas hydroxyl group at C-1 and C-5 can both increase and decrease the activity. Two glucosyl groups which were connected by C1' -> C6' showed better inhibitory activity against cancer cell lines, while the C1' -> C4' connection showed stronger inhibitory activity against the normal cell line. Also, this is the first report that the activities of these compounds exhibited different variation trends between A549 and NCI-H460 cell lines, which indicated that these compounds could selectively inhibit the cell growth. The results would lay a foundation for further research on new anti-tumor drug development
机译:在以前的研究中,从Jueptas链霉菌根的抗肿瘤部分中分离并鉴定了一系列强心苷。在本研究中,在体外评估了43种强心苷对三种细胞系(人肺A549腺癌细胞,大细胞肺癌NCI-H460细胞和正常人胎肺成纤维细胞MRC-5细胞)的细胞毒活性。大多数测试化合物对这三种细胞系显示出有效的抑制活性。然后,详细讨论了构效关系。表明C-16处的羟基和乙酰基增加了活性,而C-1和C-5处的羟基都可以增加和减少了活性。通过C1'-> C6'连接的两个葡糖基对癌细胞系表现出更好的抑制活性,而C1'-> C4'连接对正常细胞系表现出更强的抑制活性。同样,这是第一个报道,这些化合物的活性在A549和NCI-H460细胞系之间表现出不同的变化趋势,这表明这些化合物可以选择性地抑制细胞生长。该结果将为进一步研究新的抗肿瘤药物奠定基础

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