拓扑异构酶
吖啶
化学
阿姆萨克林
喜树碱
生物化学
药理学
DNA
拓扑异构酶抑制剂
吖啶衍生物
细胞毒性
立体化学
作用机理
摘要
The potential of acridines (amsacrine) as a topoisomerase II inhibitor or poison was first discovered in 1984, and since then, a considerable number of acridine derivatives have been tested as topoisomerase inhibitors/poisons, containing different substituents on the acridine chromophore. This review will discuss a series of studies published over the course of the last decade, which have investigated various novel acridine derivatives against topoisomerase II activity.
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