首页> 外文期刊>Chemical Communications >Total synthesis of (+ )-A83586C, (+ )-kettapeptin and (+ )-azinothricin: powerful new inhibitors of β-catenin/TCF4- and E2F-mediated gene transcription
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Total synthesis of (+ )-A83586C, (+ )-kettapeptin and (+ )-azinothricin: powerful new inhibitors of β-catenin/TCF4- and E2F-mediated gene transcription

机译:(+)-A83586C,(+)-kettapeptin和(+)-azinothricin的全合成:β-catenin/ TCF4-和E2F介导的基因转录的强大新抑制剂

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摘要

Herein we describe our asymmetric total syntheses of ( + )-A83586C, ( + )-kettapeptin and ( + )-azinothricin. We also demonstrate that molecules of this class powerfully inhibit β-catenin/TCF4- and E2F-mediated gene transcription within malignant human colon cancer cells at low drug concentrations.
机译:在本文中,我们描述了我们的(+)-A83586C,(+)-kettapeptin和(+)-azinothricin的不对称总合成。我们还证明,该类分子在低药物浓度下会强力抑制β-catenin/ TCF4-和E2F介导的恶性人结肠癌细胞内的基因转录。

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  • 来源
    《Chemical Communications》 |2010年第23期|P.4021-4042|共22页
  • 作者单位

    The School of Chemistry and Chemical Engineering, and the Centre for Cancer Research and Cell Biology (CCRCB), Queen 's University Belfast, Stranmillis Road, Belfast, Northern Ireland, UK BT9 SAG;

    rnThe School of Chemistry and Chemical Engineering, and the Centre for Cancer Research and Cell Biology (CCRCB), Queen 's University Belfast, Stranmillis Road, Belfast, Northern Ireland, UK BT9 SAG;

    rnDepartment of Chemistry, University of Oxford, Chemistry Research Laboratory, 12 Mansfield Road, Oxford, UK 0X1 3TA;

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  • 入库时间 2022-08-17 13:23:47

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