首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >The novel anti-tumor agents of 4-triazol-1,8-naphthalimides: synthesis, cytotoxicity, DNA intercalation and photocleavage.
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The novel anti-tumor agents of 4-triazol-1,8-naphthalimides: synthesis, cytotoxicity, DNA intercalation and photocleavage.

机译:4-三唑-1,8-萘二甲酰亚胺的新型抗肿瘤药:合成,细胞毒性,DNA嵌入和光裂解。

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摘要

A novel series of 4-(4-phenyl-[1,2,3]-triazol-1-yl)-1,8-naphthalimide derivatives had been synthesized easily by employing "click reaction". For anti-tumor activity in vitro, all the compounds were found to be more toxic against MCF-7 than Hela and 7721 cells. 4a, 4b and 4e Showed improved cytotoxic activity against MCF-7 cells over Amonafide, in particular compound 4a, with an IC(50) could amount to 10(-7) M. The UV-vis spectra and Circular Dichroism titration indicated that the compounds behaved as effective DNA-intercalating agents. The investigation of their photo-damaging ability illuminated that these compounds could damage DNA effectively into form II and even form III.
机译:通过使用“点击反应”容易地合成了一系列新的4-(4-苯基-[[1,2,3]-三唑-1-基)-1,8-萘二甲酰亚胺衍生物。对于体外抗肿瘤活性,发现所有化合物对MCF-7的毒性都比Hela和7721细胞更具毒性。图4a,4b和4e显示了优于Amonafide(特别是化合物4a)对MCF-7细胞的细胞毒活性,IC(50)可达10(-7)M。这些化合物表现为有效的DNA嵌入剂。对它们的光破坏能力的研究表明,这些化合物可以有效地破坏DNA形成II型,甚至III型。

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