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J Enzyme Inhib Med Chem ; 34(1): 1321-1346, 2019 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-31328585

RESUMEN

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.


Asunto(s)
Antineoplásicos/síntesis química , Antineoplásicos/farmacología , Carbazoles/química , Carbazoles/farmacología , Neoplasias/tratamiento farmacológico , Animales , Antineoplásicos/química , Proliferación Celular/efectos de los fármacos , Humanos , Estructura Molecular , Neoplasias/patología
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