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首页> 外文期刊>Medicinal chemistry research: an international journal for rapid communications on design and mechanisms of action of biologically active agents >Potential neurotrophic activity and cytotoxicity of selected C21 steroidal glycosides from Cynanchum otophyllum
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Potential neurotrophic activity and cytotoxicity of selected C21 steroidal glycosides from Cynanchum otophyllum

机译:潜在的神经营养活性和来自Cynanchum otophyllum所选C21甾体糖苷的细胞毒性

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摘要

Cynanchum otophyllum was traditionally used for treating muscle and skeletal pain, epilepsy, abdominal pain, and tightness. Four known C21 steroidal glycosides, namely caudatin 3-O-beta-cymaropyranoside (1), caudatin 3-O-beta-D-cymaropyranosyl-(1 -> 4)-beta-D-cymaropyranoside (2), otophylloside B (3), and otophylloside A (4) were isolated from the roots of this plant and their neurotrophic activities were examined in rat neuronal PC12 cell model, while their cytotoxicities were evaluated in human cancer cells and normal fibroblasts. Differential promoting effects on neurite-bearing cells were found among testing compounds, with 2 the most potent. On the other hand, selective cytotoxicity against human colon cancer cells HCT-116 of 2 was firstly demonstrated here. Besides, 2 induced inhibitory activities on cancer cell proliferation, sphere formation and interfered the cell cycle. The new potential pharmacological activities of 2 on colon cancer cells were revealed in the present study.
机译:Cynanchum耳科仑传统上用于治疗肌肉和骨骼疼痛,癫痫,腹痛和紧绷。 四个已知的C21甾体糖苷,即毛蛋白3-O-β-β-二氨基硼吡喃糖苷(1),尖肽3-O-β-D-氢吡喃吡喃糖基 - (1-> 4) - 滴度-d-二羟吡喃(2),卵体B(3 ),卵黄叶苷A(4)与该植物的根部分离,并在大鼠神经元PC12细胞模型中检查它们的神经营养活性,而其在人癌细胞和正常成纤维细胞中评估其细胞毒性。 在测试化合物中发现了对含有神经突含细胞的差异促进效果,具有2个最有效的。 另一方面,此处证实了对人结肠癌细胞HCT-116的选择性细胞毒性。 此外,2例诱导癌细胞增殖,球形形成和干扰细胞周期。 在本研究中揭示了在结肠癌细胞上进行的新潜在药理活性。

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