Pyrrolocarbazoles as checkpoint 1 kinase inhibitors |
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Authors: | Hénon Hélène Conchon Elisabeth Hugon Bernadette Messaoudi Samir Golsteyn Roy M Prudhomme Michelle |
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Affiliation: | Laboratoire SEESIB, Université Blaise Pascal, UMR 6504 du CNRS, 24 Avenue des Landais, 63177 Aubière, France. Michelle.PRUDHOMME@univ-bpclermont.fr |
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Abstract: | The carbazole framework is found in many natural compounds of biological interest. Indolocarbazoles such as rebeccamycin and staurosporine which are either a topoisomerase I inhibitor (rebeccamycin) or a non selective kinase inhibitor (staurosporine) are bacterial metabolites. In the search for new antitumor agents, DNA damage checkpoint kinases, in particular Checkpoint kinase 1, have recently emerged as attractive targets for cancer therapy. This review reports the synthesis and Chk1 inhibitory activities of pyrrolocarbazole compounds bearing four or five fused rings. |
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