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A Review of the Structure—Activity Relationship of Natural and Synthetic Antimetastatic Compounds

机译:天然和合成抗转移化合物的结构-活性关系的综述

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摘要

There are innumerable anticancer compounds derived from either natural or synthetic origins. Many of these compounds have been further developed through structural modifications to not only inhibit cancer cell growth but also to exert an antimetastatic effect. This is achieved by attaching different substituents to generate different structure—activity relationships. This review highlights the effectiveness of different functional groups known to have antimigration and antiproliferation activities, such as fluoro, methoxy, methyl, amino, hydroxy, nitro, bromo, chloro, methylamino, ethoxy, carbonyl, iodo, and trifluoromethyl groups. Additionally, the positioning of these functional groups plays an important role in their anticancer activities, which was evident in one of our studies comparing analogues of a natural compound. Thus, this review suggests future recommendations for the design and development of improved anticancer drugs with higher efficacy.
机译:有无数的天然或合成来源的抗癌化合物。这些化合物中的许多已通过结构修饰进一步开发,不仅抑制癌细胞的生长,而且发挥抗转移作用。这是通过连接不同的取代基以生成不同的结构-活性关系来实现的。这篇综述强调了已知具有抗迁移和抗扩散活性的不同官能团的有效性,例如氟,甲氧基,甲基,氨基,羟基,硝基,溴,氯,甲氨基,乙氧基,羰基,碘和三氟甲基。此外,这些官能团的定位在其抗癌活性中起着重要作用,这在我们比较天然化合物类似物的一项研究中很明显。因此,本综述提出了设计和开发具有更高功效的改良抗癌药物的未来建议。

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