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Synthesis of Cortistatins A, J, K, and L

The cortistatins are a recently identified class of marine natural products characterized by an unusual steroidal skeleton and have been found to inhibit differentially the proliferation of various mammalian cells in culture by an unknown mechanism. We describe a comprehensive route for the synthesi...

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Detalles Bibliográficos
Autores principales: Flyer, Alec N., Si, Chong, Myers, Andrew G.
Formato: Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2946095/
https://www.ncbi.nlm.nih.gov/pubmed/20861906
http://dx.doi.org/10.1038/nchem.794
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author Flyer, Alec N.
Si, Chong
Myers, Andrew G.
author_facet Flyer, Alec N.
Si, Chong
Myers, Andrew G.
author_sort Flyer, Alec N.
collection PubMed
description The cortistatins are a recently identified class of marine natural products characterized by an unusual steroidal skeleton and have been found to inhibit differentially the proliferation of various mammalian cells in culture by an unknown mechanism. We describe a comprehensive route for the synthesis of cortistatins from a common precursor, which in turn is assembled from two fragments of similar structural complexity. Cortistatins A and J, and for the first time, K and L, have been synthesized in parallel processes from like intermediates prepared from a single compound. With the identification of facile laboratory transformations linking intermediates in the cortistatin L synthetic series with corresponding intermediates to cortistatins A and J, we have been led to speculate that somewhat related paths might occur in nature, offering potential sequencing and chemical detail for cortistatin biosynthetic pathways.
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spelling pubmed-29460952011-04-01 Synthesis of Cortistatins A, J, K, and L Flyer, Alec N. Si, Chong Myers, Andrew G. Nat Chem Article The cortistatins are a recently identified class of marine natural products characterized by an unusual steroidal skeleton and have been found to inhibit differentially the proliferation of various mammalian cells in culture by an unknown mechanism. We describe a comprehensive route for the synthesis of cortistatins from a common precursor, which in turn is assembled from two fragments of similar structural complexity. Cortistatins A and J, and for the first time, K and L, have been synthesized in parallel processes from like intermediates prepared from a single compound. With the identification of facile laboratory transformations linking intermediates in the cortistatin L synthetic series with corresponding intermediates to cortistatins A and J, we have been led to speculate that somewhat related paths might occur in nature, offering potential sequencing and chemical detail for cortistatin biosynthetic pathways. 2010-08-01 2010-10 /pmc/articles/PMC2946095/ /pubmed/20861906 http://dx.doi.org/10.1038/nchem.794 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Flyer, Alec N.
Si, Chong
Myers, Andrew G.
Synthesis of Cortistatins A, J, K, and L
title Synthesis of Cortistatins A, J, K, and L
title_full Synthesis of Cortistatins A, J, K, and L
title_fullStr Synthesis of Cortistatins A, J, K, and L
title_full_unstemmed Synthesis of Cortistatins A, J, K, and L
title_short Synthesis of Cortistatins A, J, K, and L
title_sort synthesis of cortistatins a, j, k, and l
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2946095/
https://www.ncbi.nlm.nih.gov/pubmed/20861906
http://dx.doi.org/10.1038/nchem.794
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