Substituted indole compounds and methods of their use
    7.
    发明授权
    Substituted indole compounds and methods of their use 失效
    取代的吲哚化合物及其使用方法

    公开(公告)号:US06372742B1

    公开(公告)日:2002-04-16

    申请号:US09608861

    申请日:2000-06-30

    IPC分类号: A61K314166

    摘要: 5-(3-Isatinylidinyl)thiazolidineones and 3-(thiazolidinon-5-yl)indoles compounds, compositions, and methods of inhibiting telomerase activity in vitro and treatment of telomerase mediated conditions or diseases ex vivo and in vivo are provided. The methods, compounds and compositions of the invention may be employed alone, or in combination with other pharmacologically active agents in the treatment of conditions or diseases mediated by telomerase activity, such as in the treatment of cancer. Also disclosed are novel methods for assaying or screening for inhibitors of telomerase activity.

    摘要翻译: 提供5-(3-异
    吲嗪基)噻唑烷酮和3-(噻唑烷酮-5-基)吲哚化合物,组合物和体外抑制端粒酶活性的方法以及离体和体内治疗端粒酶介导的病症或疾病。 本发明的方法,化合物和组合物可以单独使用或与其它药理学活性剂组合用于治疗由端粒酶活性介导的病症或疾病,例如治疗癌症。 还公开了用于测定或筛选端粒酶活性抑制剂的新方法。

    Cancer treatment by combined inhibition of proteasome and telomerase activities
    8.
    发明授权
    Cancer treatment by combined inhibition of proteasome and telomerase activities 有权
    癌症治疗联合抑制蛋白酶体和端粒酶活性

    公开(公告)号:US07998938B2

    公开(公告)日:2011-08-16

    申请号:US11918581

    申请日:2006-04-14

    IPC分类号: A16K48/00

    摘要: A method and kit for inhibiting the proliferation of cancer cells are disclosed, based on a combination of a proteasome inhibitor and a telomerase inhibitor. When used in cancer therapy, the two compounds in combination enhance the anti-cancer treatment efficacy obtained with the proteasome inhibitor alone or the telomerase inhibitor alone. Preferably, efficacy is supraadditive or synergistic in nature relative to the combined effects of the individual agents, with minimal exacerbation of side effects.

    摘要翻译: 基于蛋白酶体抑制剂和端粒酶抑制剂的组合,公开了抑制癌细胞增殖的方法和试剂盒。 当用于癌症治疗时,两种化合物组合增强了单独使用蛋白酶体抑制剂或单独使用端粒酶抑制剂获得的抗癌治疗功效。 优选地,相对于各个试剂的组合效应,效力是相对于辅助的或协同的,并且副作用的加剧最小化。