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首页> 外文期刊>Letters in Drug Design & Discovery >Design, Synthesis and Biological Activity of A-C8/C-C2-Linked 6-Chloropurine-Pyrrolobenzodiazepine Hybrids as Anticancer Agents
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Design, Synthesis and Biological Activity of A-C8/C-C2-Linked 6-Chloropurine-Pyrrolobenzodiazepine Hybrids as Anticancer Agents

机译:抗癌剂A-C8 / C-C2-连接的6-氯嘌呤-吡咯并苯并二氮杂杂化物的设计,合成及生物活性

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摘要

New A-C8 and C-C2-linked 6-chloropurine-pyrrolo[2,1-c][1,4]benzodiazepine hybrids have been prepared and evaluated for their anticancer potential. The molecular modeling studies might be explained in terms of effect of the molecule on binding in the minor groove of DNA and also comparison to both A-C8/C-C2-position of the PBD. These PBD conjugates have shown DNA-binding ability and promising anticancer activity.
机译:已经制备了新的A-C8和C-C2连接的6-氯嘌呤-吡咯并[2,1-c] [1,4]苯并二氮杂杂化物,并评估了它们的抗癌潜力。可以通过分子对DNA小沟中结合的影响以及与PBD的A-C8 / C-C2位置的比较来解释分子模型研究。这些PBD偶联物已显示出DNA结合能力和有希望的抗癌活性。

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