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Gold(I) complex of N,N'-disubstituted cyclic thiourea with in vitro and in vivo anticancer properties-potent tight-binding inhibition ofthioredoxin reductase

机译:N,N'-二取代的环硫脲的金(I)配合物具有体内和体外的抗癌特性-对硫氧还蛋白还原酶的紧密结合抑制作用

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摘要

Coinage metal complexes of an N,N-disubstituted cyclic thiourea exert significant cytotoxicities to cancer cells and, in particular, the gold(I) thiourea complex exhibits a potent tight-binding inhibition of the anticancer drug target thioredoxin reductase with an inhibitory constant at nanomolar level.
机译:N,N-二取代的环状硫脲的纽币金属络合物对癌细胞具有显着的细胞毒性,特别是,金(I)硫脲络合物表现出对抗癌药物靶标硫氧还蛋白还原酶的强力紧密结合抑制作用,且在纳摩尔浓度具有抑制常数水平。

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  • 来源
    《Chemical Communications》 |2010年第41期|p.7691-7693|共3页
  • 作者单位

    Department of Chemistry and Open Laboratory of Chemical Biology of the Institute of Molecular Technology for Drug Discovery and Synthesis, The University of Hong Kong, Pokfulam Road,Hong Kong, China;

    rnDepartment of Chemistry and Open Laboratory of Chemical Biology of the Institute of Molecular Technology for Drug Discovery and Synthesis, The University of Hong Kong, Pokfulam Road,Hong Kong, China;

    rnCNRS/UPPA, Laboratory of Bio-Inorganic Analytical andEnvironmental Chemistry, UMR5254, Helioparc, 2 Av. Pr. Angot,F-64053, Pan, France;

    rnDepartment of Chemistry and Open Laboratory of Chemical Biology of the Institute of Molecular Technology for Drug Discovery and Synthesis, The University of Hong Kong, Pokfulam Road,Hong Kong, China;

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