Review Article

类黄酮作为P-gp抑制剂:SAR的系统评价

卷 26, 期 25, 2019

页: [4799 - 4831] 页: 33

弟呕挨: 10.2174/0929867325666181001115225

价格: $65

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摘要

P-糖蛋白在ABC转运蛋白家族中也称为ABCB1,它使转移癌细胞对具有不同靶标和不同化学结构的各种抗癌药物同时具有抗性。 在过去的四十年中,对这种泵的安全和特定抑制剂的探索一直是科学家追求的目标。 天然存在的类黄酮作为苯并吡喃酮衍生物被认为是P-gp的一类无毒抑制剂。 合成类黄酮二聚体FD18作为在体内外逆转多药耐药性的有效P-gp调节剂的最新出现,特别针对药物转运蛋白的假二聚体结构,并代表了具有高转运蛋白结合亲和力和低抑菌剂的新一代抑制剂。 毒性。 该综述涉及临床前研究中类黄酮作为P-gp抑制剂的结构-活性关系的最新进展,其作用的分子机制以及克服P-gp介导的MDR的能力。 它对发现可调节ABC转运蛋白外排的新药候选物具有至关重要的意义,也为该有前途的领域的未来发展提供了一些线索。

关键词: P-糖蛋白,多药耐药,类黄酮,抑制剂,SAR,抗癌

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