Title:The Syntheses and Medicinal Attributes of Phenanthrenes as Anticancer
Agents: A Quinquennial Update
Volume: 29
Issue: 20
关键词:
抗癌,DNA插层,菲,分子对接,构效关系,药物化学。
摘要: 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.