Journal of Enzyme Inhibition and Medicinal Chemistry (Jan 2019)

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

  • Samar Issa,
  • Anthony Prandina,
  • Nicolas Bedel,
  • Pål Rongved,
  • Saïd Yous,
  • Marc Le Borgne,
  • Zouhair Bouaziz

DOI
https://doi.org/10.1080/14756366.2019.1640692
Journal volume & issue
Vol. 34, no. 1
pp. 1321 – 1346

Abstract

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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.

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