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'MULTI-TARGET' COMPOUNDS INHIBITORING HISTONE-DESACETYLASES AND POLYMERIZATION OF TUBULIN FOR USE IN THE TREATMENT OF CANCER

机译:抑制组蛋白去乙酰化和微管蛋白聚合的“多靶点”化合物,用于治疗癌症

摘要

The present invention relates to the design of novel so-called “multi-target” molecules possessing a double pharmacophore and acting both as inhibitors of histone deacetylases (HDACs) and as inhibitors of the polymerization of tubulin. The invention also describes the process for synthesizing “multi-target” molecules and their application in the treatment of cancer, a pharmaceutical composition comprising at least one “multi-target” molecule, as well as the use of such compositions in the treatment. cancer.
机译:本发明涉及具有双重药效团并且既充当组蛋白脱乙酰基酶(HDAC)的抑制剂又充当微管蛋白聚合的抑制剂的新颖的所谓“多靶标”分子的设计。本发明还描述了合成“多靶标”分子的方法及其在癌症治疗中的应用,包含至少一个“多靶标”分子的药物组合物,以及这种组合物在治疗中的用途。癌症。

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