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Nano-cuprous oxide catalyzed one-pot synthesis of a carbazole-based STAT3 inhibitor: a facile approach via intramolecular C-N bond formation reactions

机译:纳米氧化氧化物催化一锅合成的基于咔唑的STAT3抑制剂:通过分子内C-N键形成反应的容易方法

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摘要

In this study, we report the one-pot synthesis of substituted carbazole derivatives using nano cuprous oxide as a catalyst via intramolecular C-N bond forming reactions. Among the synthesized carbazoles, 3'-((3-acetyl-6-chloro-9H-carbazol-9-yl) methyl)-[1,10-biphenyl]-2-carbonitrile (ACB) was identified as a lead antiproliferative agent against lung cancer cell lines A549 and LLC with an IC50 of 13.6 and 16.4 mu M respectively. Furthermore, we found that the lead compound suppresses the constitutive phosphorylation of STAT3 (Tyr-705) in A549, HCC-2279 and H1975 cells. We analyzed the levels of phospho-STAT3 and LSD1 in the nuclear extract of ACB treated HCC-2279 cells to evaluate the transcriptional activity of STAT3. We found the downregulation of phospho-STAT3 without any change in the expression of LSD1 indicating that ACB downregulates the transcriptional activity of STAT3. Molecular docking analysis revealed that ACB makes a favorable interaction with Arg-609 and Ser-613 in the pTyr site of the SH2 domain of STAT3.
机译:在该研究中,通过分子内C-N键形成反应报告使用纳米亚铜作为催化剂的取代咔唑衍生物的单罐合成。在合成的咔唑中,3' - ((3-乙酰-6-氯-9H-咔唑-9-基)甲基) - [1,10-联苯基] -2-碳腈(ACB)被鉴定为铅抗增殖剂对肺癌细胞系A549和LLC分别为13.6和16.4μm的IC50。此外,我们发现铅化合物抑制了A549,HCC-2279和H1975细胞中STAT3(TYR-705)的组成型磷酸化。我们分析了ACB治疗HCC-2279细胞核提取物中磷酸盐-TAT3和LSD1的水平,以评估STAT3的转录活性。我们发现磷酸盐 - STAT3的下调,没有LSD1表达的任何变化,表明ACB下调STAT3的转录活性。分子对接分析显示,ACB在STAT3的SH2结构域的PTYR位点中与ARG-609和SER-613进行有利的相互作用。

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  • 来源
    《RSC Advances》 |2016年第43期|共11页
  • 作者单位

    Bangalore Univ Dept Chem Biol Chem Lab Cent Coll Campus Palace Rd Bangalore 560001 Karnataka India;

    Univ Mysore Dept Studies Chem Mysore 570006 Karnataka India;

    Bal Pharma Ltd 61-B Bommasandra Bangalore 560099 Karnataka India;

    Hokkaido Univ Frontier Res Ctr Postgenome Sci &

    Technol Sapporo Hokkaido 0600808 Japan;

    Natl Univ Singapore Canc Sci Inst Singapore Singapore 117599 Singapore;

    Bangalore Univ Dept Chem Biol Chem Lab Cent Coll Campus Palace Rd Bangalore 560001 Karnataka India;

    Univ Cambridge Dept Chem Ctr Mol Informat Lensfield Rd Cambridge CB2 1EW England;

    Univ Cambridge Dept Chem Ctr Mol Informat Lensfield Rd Cambridge CB2 1EW England;

    Natl Univ Singapore Canc Sci Inst Singapore Singapore 117599 Singapore;

    Bangalore Univ Dept Chem Biol Chem Lab Cent Coll Campus Palace Rd Bangalore 560001 Karnataka India;

    Univ Mysore Dept Studies Chem Mysore 570006 Karnataka India;

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  • 正文语种 eng
  • 中图分类 化学;
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