Carbazole scaffolds in cancer therapy: a review from 2012 to 2018

被引:120
作者
Issa, Samar [1 ]
Prandina, Anthony [2 ]
Bedel, Nicolas [2 ]
Rongved, Pal [3 ]
Yous, Said [4 ]
Le Borgne, Marc [2 ]
Bouaziz, Zouhair [2 ]
机构
[1] EBInnov, Ecole Biol Ind, 49 Ave Genottes,CS90009, F-95895 Cergy Pontoise, France
[2] Univ Claude Bernard Lyon 1, Univ Lyon, SFR Sante Lyon Est CNRS UMS3453 INSERM US7, EA 4446 Bioact Mol & Med Chem,Fac Pharm ISPB, Lyon, France
[3] Univ Oslo, Sch Pharm, Dept Pharmaceut Chem, Oslo, Norway
[4] Univ Lille, INSERM, UMR S 1172 JPArc Ctr Rech Jean Pierre Aubert Neur, CHU Lille, Lille, France
关键词
Carbazole; cancer; cytotoxicity; targeted therapy; enzyme inhibitors; POTENT ANTITUMOR-ACTIVITY; BIOLOGICAL EVALUATION; ANTIPROLIFERATIVE EVALUATION; CYTOTOXIC ACTIVITIES; ANTICANCER ACTIVITY; MOLECULAR DOCKING; PYRAZOLE ANALOGS; NATURAL-PRODUCTS; VISIBLE-LIGHT; ALK INHIBITOR;
D O I
10.1080/14756366.2019.1640692
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
For over half a century, the carbazole skeleton has been the key structural motif of many biologically active compounds including natural and synthetic products. Carbazoles have taken an important part in all the existing anti-cancer drugs because of their discovery from a large variety of organisms, including bacteria, fungi, plants, and animals. In this article, we specifically explored the literature from 2012 to 2018 on the anti-tumour activities reported to carbazole derivatives and we have critically collected the most significant data. The most described carbazole anti-tumour agents were classified according to their structure, starting from the tricyclic-carbazole motif to fused tetra-, penta-, hexa- and heptacyclic carbazoles. To date, three derivatives are available on the market and approved in cancer therapy.
引用
收藏
页码:1321 / 1346
页数:26
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