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1,8-萘二甲酰亚胺:一种有效的DNA嵌入剂及癌症治疗靶点。

1,8-Naphthalimide: A Potent DNA Intercalator and Target for Cancer Therapy.

作者信息

Tandon Runjhun, Luxami Vijay, Kaur Harsovin, Tandon Nitin, Paul Kamaldeep

机构信息

Department of Chemistry, School of Physical Sciences, Lovely, Professional University, Phagwara-, 144411, India.

School of Chemistry and Biochemistry, Thapar University, Patiala-, 147004, India.

出版信息

Chem Rec. 2017 Oct;17(10):956-993. doi: 10.1002/tcr.201600134. Epub 2017 Apr 4.

Abstract

The poor pharmacokinetics, side effects and particularly the rapid emergence of drug resistance compromise the efficiency of clinically used anticancer drugs. Therefore, the discovery of novel and effective drugs is still an extremely primary mission. Naphthalimide family is one of the highly active anticancer drug based upon effective intercalator with DNA. In this article, we review the discovery and development of 1,8-naphthalimide moiety, and, especially, pay much attention to the structural modifications and structure activity relationships. The review demonstrates how modulation of the moiety affecting naphthalimide compound for DNA binding that is achieved to afford a profile of antitumor activity. The DNA binding of imide and ring substitution at naphthalimide, bisnaphthalimide, naphthalimide-metal complexes is achieved by molecular recognition through intercalation mode. Thus, this synthetic/natural small molecule can act as a drug when activation or inhibition of DNA function, is required to cure or control the cancer disease. The present study is a review of the advances in 1,8-naphthalimide-related research, with a focus on how such derivatives are intercalated into DNA for their anticancer activities.

摘要

临床使用的抗癌药物存在药代动力学不佳、副作用大,尤其是耐药性迅速出现等问题,影响了其疗效。因此,发现新型有效药物仍然是一项极其重要的任务。萘酰亚胺家族是基于与DNA有效嵌入剂的高活性抗癌药物之一。在本文中,我们综述了1,8-萘酰亚胺部分的发现与发展,尤其关注其结构修饰和构效关系。该综述展示了如何通过调节该部分来影响萘酰亚胺化合物与DNA的结合,从而获得抗肿瘤活性。萘酰亚胺、双萘酰亚胺、萘酰亚胺-金属配合物中酰亚胺的DNA结合以及萘环上的取代是通过嵌入模式的分子识别实现的。因此,当需要激活或抑制DNA功能以治疗或控制癌症疾病时,这种合成/天然小分子可以用作药物。本研究综述了1,8-萘酰亚胺相关研究的进展,重点关注此类衍生物如何嵌入DNA以发挥其抗癌活性。

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