首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis and antitumour activity of new dendritic polyamines-(imide-DNA-intercalator) conjugates: potent Lck inhibitors.
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Synthesis and antitumour activity of new dendritic polyamines-(imide-DNA-intercalator) conjugates: potent Lck inhibitors.

机译:新型树突状多胺-(酰亚胺-DNA-嵌入剂)结合物的合成及其抗肿瘤活性:强力的Lck抑制剂。

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摘要

A series of dendritic polyamines-(imide-DNA-intercalators) conjugates with different connectivity in their basic chain were synthesised and evaluated as antitumour compounds. Although their antiproliferative activity against HT-29 was not significant, conjugates 13 and 16 showed a promising profile as inhibitors of Lck.
机译:合成了一系列在其基本链上具有不同连接性的树状多胺-(酰亚胺-DNA-嵌入剂)结合物,并将其作为抗肿瘤化合物进行了评估。尽管它们对HT-29的抗增殖活性不明显,但是缀合物13和16作为Lck的抑制剂显示出有希望的概况。

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