基于膦酸酯骨架的氨基酸衍生物的合成与抗肿瘤作用
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贵州省科技厅国际合作基金


Synthesis and Antitumor Activity of Amino Acid Derivatives Containing Phosphonate backbones
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    摘要:

    为了获取抗肿瘤活性化合物,通过拼合原理,设计合成了9个目标化合物,经IR, 1HNMR, 13CNMR及元素分析确认结构。采用溴化噻唑蓝四氮唑(MTT)法进行了抗肿瘤活性测试。结果表明,该类化合物对所测肿瘤细胞有增殖抑制作用,其中化合物Ⅲf、Ⅲi有较好抗肿瘤活性,尤以Ⅲi最为突出,对肿瘤细胞A-549、SGC-7901和EC-109均有显著抑制作用,IC50分别为(7.0±0.8)、(6.9±0.8)、(7.3±0.7)μ mol/L,与对照药cisplatin相当。该类化合物值得进一步研究。

    Abstract:

    In search of more effective anticancer agents, according to the combination principle, 9 phosphonate derivatives were designed and synthesized. Their structures were clearly established by elemental analysis, IR, 1HNMR and 13CNMR, and their antiproliferative activities were evaluated against some tumor cell lines by using a methylthiazolyldiphenyl- tetrazolium bromide (MTT) method. Preliminary results in bioactivity tests indicated that they exhibited certain antitumor activities. Among the active compounds, compounds Ⅲf, Ⅲi had better inhibition effect on cells growth, espectively, compounds Ⅲi showed remarkable activities against A-549, SGC-7901 and EC-109 with IC50 values of 7.0±0.8, 6.9±0.8 and 7.3±0.7 μmol/L respectively, similar to cisplatin, which were worth further investigation.

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杨家强.基于膦酸酯骨架的氨基酸衍生物的合成与抗肿瘤作用[J].精细化工,2016,33(5):0

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  • 收稿日期:2016-01-27
  • 最后修改日期:2016-02-22
  • 录用日期:2016-02-25
  • 在线发布日期: 2016-04-12
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