Current status of carbazole hybrids as anticancer agents

被引:63
作者
Wang, Gangqiang [1 ,2 ]
Sun, Shaofa [1 ]
Guo, Hua [3 ]
机构
[1] Hubei Univ Sci & Technol, Sch Nucl Technol & Chem & Biol, Nonpower Nucl Technol Collaborat Innovat Ctr, Hubei Key Lab Radiat Chem & Funct Mat, Xianning 437100, Peoples R China
[2] South Cent Univ National, Sch Pharmaceut Sci, Wuhan 430074, Peoples R China
[3] Anshan Normal Univ, Sch Chem & Life Sci, Anshan 114005, Liaoning, Peoples R China
关键词
Carbazole; Hybrid molecules; Cancer; Drug resistance; Structure-activity relationships; Mechanisms of action; VITRO ANTIPROLIFERATIVE ACTIVITY; MOLECULAR DOCKING; BIOLOGICAL EVALUATION; CYTOTOXIC ACTIVITY; ANTITUMOR-ACTIVITY; DERIVATIVES; DESIGN; POTENT; INHIBITORS; SCAFFOLD;
D O I
10.1016/j.ejmech.2021.113999
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The drug resistance and low specificity of current available chemotherapeutics to cancer cells are the main reasons responsible for the failure of cancer chemotherapy and remain dramatic challenges for cancer therapy, creating an urgent need to develop novel anticancer agents. Carbazole nucleus, widely distributed in nature, is a predominant feature of a vast array of biologically active compounds. Carbazole derivatives exhibited potential antiproliferative activity against different cancer cell lines by diverse mechanisms, inclusive of arrest cell cycle and induce apoptosis, and several anticancer agents are carbazole-based compounds. Thus, carbazole derivatives represent a fertile source for discovery of novel anticancer therapeutic agents. Over the past several years, a variety of carbazole hybrids have been developed as potential anticancer agents. The present review focuses on the recent progress, from 2016 until now, in knowledge on anticancer properties, structure-activity relationships and mechanisms of action of carbazole hybrids to provide a basis for development of relevant therapeutic agents. (c) 2021 Elsevier Masson SAS. All rights reserved.
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页数:15
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