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首页> 外文期刊>Phytochemistry >Bufadienolide glycosides and bufadienolides from the whole plants of Helleborus lividus, and their cytotoxic activity
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Bufadienolide glycosides and bufadienolides from the whole plants of Helleborus lividus, and their cytotoxic activity

机译:来自Helleborus Lividus的整株植物的Bufdienolide糖苷和Bufdienolides及其细胞毒性活性

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摘要

Cytotoxicity-guided fractionation of the MeOH extract of Hellebores lividus Aiton ex Curtis (Ranunculaceae) resulted in the isolation of five undescribed bufadienolide glycosides and two undescribed bufadienolides, along with three known compounds. Their structures were determined by detailed spectroscopic analysis and hydrolysis studies. The isolated compounds showed cytotoxicity against HL-60 human leukemia cells and A549 human lung adenocarcinoma cells, with IC50 values ranging from 2.20 +/- 0.01 nM to 0.77 +/- 0.01 mu M. The undescribed compound 3 beta-[(O-beta-D-glucopyranosyl-(1 -> 4)-alpha-L-rhamnopyranosyl)oxyl-14 beta,16 beta-dihydroxy-5 beta-bufa-20,22-dienolide induced apoptosis in HL-60 cells via a mitochondria-dependent apoptotic pathway. The average IC50, values of bufadienolide monorhamnosides for HL-60 and A549 cells were 10-20 times lower than those for Na+/K+ ATPase, implying that they induce tumor cell death via a mechanism of action other than Na+/K+ ATPase inhibition.
机译:Hellebores Lividus Aiton Ex Curtis(毛茛科)的细胞毒性引导分馏导致五种未描述的Bufdienolide糖苷和两个未描述的BufdiNolides,以及三种已知的化合物。通过详细的光谱分析和水解研究确定它们的结构。分离的化合物对HL-60人白血病细胞和A549人肺腺癌细胞进行细胞毒性,IC50值范围从2.20 +/- 0.01nm至0.77 +/- 0.01 mu m。未思索的化合物3β-[(O-β -D-吡喃葡萄糖基 - (1-> 4) - α-L-萘吡喃糖基)oxyl-14β,16β-二羟基-5β-bufa-20,22-促蛋白质通过依赖于线粒体依赖于Mitochondria的HL-60细胞诱导细胞凋亡凋亡途径。平均IC50,HL-60和A549细胞的Bufdienolide单红烃的值低于Na + / K + AtP酶的10-20倍,这意味着它们通过除Na + / K + AtPase抑制之外的作用机制诱导肿瘤细胞死亡。

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