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Marine Pyrrolocarbazoles and Analogues: Synthesis and Kinase Inhibition
Granulatimide and isogranulatimide are alkaloids obtained from marine sources which have been shown to inhibit cell-cycle G2-checkpoint, targeting more particularly checkpoint 1 kinase (Chk1). At a structural level, they possess a characteristic pyrrolocarbazole framework also shared by the well-kno...
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Formato: | Texto |
Lenguaje: | English |
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Molecular Diversity Preservation International
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2810226/ https://www.ncbi.nlm.nih.gov/pubmed/20098609 http://dx.doi.org/10.3390/md7040754 |
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author | Deslandes, Sébastien Chassaing, Stefan Delfourne, Evelyne |
author_facet | Deslandes, Sébastien Chassaing, Stefan Delfourne, Evelyne |
author_sort | Deslandes, Sébastien |
collection | PubMed |
description | Granulatimide and isogranulatimide are alkaloids obtained from marine sources which have been shown to inhibit cell-cycle G2-checkpoint, targeting more particularly checkpoint 1 kinase (Chk1). At a structural level, they possess a characteristic pyrrolocarbazole framework also shared by the well-known rebeccamycin and staurosporine microbial metabolites which have been described to inhibit topoisomerase I and diverse kinases, respectively. This review reports precisely on the synthesis and kinase inhibitory activities of pyrrolocarbazole-based analogues of granulatimide. |
format | Text |
id | pubmed-2810226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Molecular Diversity Preservation International |
record_format | MEDLINE/PubMed |
spelling | pubmed-28102262010-01-22 Marine Pyrrolocarbazoles and Analogues: Synthesis and Kinase Inhibition Deslandes, Sébastien Chassaing, Stefan Delfourne, Evelyne Mar Drugs Review Granulatimide and isogranulatimide are alkaloids obtained from marine sources which have been shown to inhibit cell-cycle G2-checkpoint, targeting more particularly checkpoint 1 kinase (Chk1). At a structural level, they possess a characteristic pyrrolocarbazole framework also shared by the well-known rebeccamycin and staurosporine microbial metabolites which have been described to inhibit topoisomerase I and diverse kinases, respectively. This review reports precisely on the synthesis and kinase inhibitory activities of pyrrolocarbazole-based analogues of granulatimide. Molecular Diversity Preservation International 2009-12-01 /pmc/articles/PMC2810226/ /pubmed/20098609 http://dx.doi.org/10.3390/md7040754 Text en © 2009 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Deslandes, Sébastien Chassaing, Stefan Delfourne, Evelyne Marine Pyrrolocarbazoles and Analogues: Synthesis and Kinase Inhibition |
title | Marine Pyrrolocarbazoles and Analogues: Synthesis and Kinase Inhibition |
title_full | Marine Pyrrolocarbazoles and Analogues: Synthesis and Kinase Inhibition |
title_fullStr | Marine Pyrrolocarbazoles and Analogues: Synthesis and Kinase Inhibition |
title_full_unstemmed | Marine Pyrrolocarbazoles and Analogues: Synthesis and Kinase Inhibition |
title_short | Marine Pyrrolocarbazoles and Analogues: Synthesis and Kinase Inhibition |
title_sort | marine pyrrolocarbazoles and analogues: synthesis and kinase inhibition |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2810226/ https://www.ncbi.nlm.nih.gov/pubmed/20098609 http://dx.doi.org/10.3390/md7040754 |
work_keys_str_mv | AT deslandessebastien marinepyrrolocarbazolesandanaloguessynthesisandkinaseinhibition AT chassaingstefan marinepyrrolocarbazolesandanaloguessynthesisandkinaseinhibition AT delfourneevelyne marinepyrrolocarbazolesandanaloguessynthesisandkinaseinhibition |