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Synthesis and in vitro evaluation of naphthalimide-benzimidazole conjugates as potential antitumor agents

机译:萘二甲酰亚胺-苯并咪唑共轭物作为潜在抗肿瘤药的合成及体外评价

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摘要

A series of novel naphthalimide-benzimidazoles was designed and synthesized for the first time and studied for their effect on antiproliferative activity. Some of these compounds possessed good antitumor activity towards the tested cancer cell lines. Noticeably, (diethylamino) ethyl 15 and (dimethylamino) ethyl 23 derivatives displayed superior antiproliferative activity towards human cancer cell lines with MG_MID GI(50) values of 1.43 and 1.83 mu M, respectively. Preliminary investigation revealed that compounds 15 and 23 might bind with ct-DNA through the intercalation mode which is responsible for potent bioactivity. Moreover, transportation behaviour indicated that these molecules could efficiently bind to and be carried by bovine albumin, and the hydrogen bonding and hydrophobic interactions played important roles in interaction with serum albumin.
机译:首次设计和合成了一系列新型的萘二甲酰亚胺-苯并咪唑,并研究了它们对抗增殖活性的影响。这些化合物中的一些对所测试的癌细胞系具有良好的抗肿瘤活性。值得注意的是,(二乙氨基)乙基15和(二甲氨基)乙基23衍生物对人癌细胞系的MG_MID GI(50)值分别为1.43和1.83μM,显示出优异的抗增殖活性。初步研究表明,化合物15和23可能通过插入模式与ct-DNA结合,而插入模式负责有效的生物活性。此外,运输行为表明这些分子可以有效地结合并被牛白蛋白携带,并且氢键和疏水相互作用在与血清白蛋白的相互作用中起重要作用。

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  • 来源
    《Organic & biomolecular chemistry》 |2019年第21期|5349-5366|共18页
  • 作者单位

    Thapar Univ, Sch Chem & Biochem, Patiala 147004, Punjab, India;

    Thapar Univ, Sch Chem & Biochem, Patiala 147004, Punjab, India;

    Thapar Univ, Sch Chem & Biochem, Patiala 147004, Punjab, India;

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