期刊
CURRENT MEDICINAL CHEMISTRY
卷 29, 期 20, 页码 3530-3556出版社
BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/0929867328666211018110223
关键词
Anticancer; DNA intercalation; phenanthrene; molecular docking; structure-activity relationship; medicinal chemistry
资金
- Department of Pharmaceuticals (DoP), Ministry of Chemicals & Fertilizers, Govt. of India, New Delhi
Cancer, as a global health issue, poses a significant threat to human lives. DNA, being one of the major targets in cancer chemotherapy, can be effectively targeted by phenanthrene and its derivatives through intercalation and inhibition of DNA synthesis enzymes. However, the development of novel chemotherapeutic agents is crucial due to off-target effects and resistance. This review summarizes the recent progress in the development of phenanthrene-based derivatives, focusing on synthetic strategies, conjugation with other pharmacophores, and metal complexes. The cytotoxicity evaluation against various carcinoma cell lines and computational studies are also discussed, highlighting the potential of these derivatives as cytotoxic agents in medicinal chemistry.
Cancer is a silent killer and remains to pose major health problems globally. Amongst the several biological targets, DNA is one of the most striking targets in cancer chemotherapy. Owing to its planar structure, phenanthrene and its derivatives exhibit potential cytotoxicity by intercalating between the DNA base pairs and by inhibiting the enzymes that are involved in the synthesis of DNA. However, due to the off-target effects and resistance, the development of novel chemotherapeutic agents would be meritorious. In this regard, we present a detailed review on the development of phenanthrene-based derivatives reported in the last quinquennial. This review mainly focuses on the synthetic aspects and strategies to procure the fused phenanthrene derivatives such as (i) phenanthroindolizidines, phenanthroquinolizidine, phenanthroimidazoles, podophyllotoxin-based phenanthrenes, and dihydrophenanthrodioxine derivatives, (ii) phenanthrene conjugates with other pharmacologically significant pharmacophores, and (iii) phenanthrene-metal complexes. This review also edifies their potential in vitro cytotoxicity evaluation against various carcinoma cell lines in submicromolar to nanomolar ranges. Additionally, computational studies and structure-activity relationships (SARs) have also been presented to highlight the essential features of the designed congeners. Thus, this review would aid in the development of novel derivatives in future as potential cytotoxic agents in the field of medicinal chemistry.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据