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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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Formato: | Texto |
Lenguaje: | English |
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2010
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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. |
format | Text |
id | pubmed-2946095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT flyeralecn synthesisofcortistatinsajkandl AT sichong synthesisofcortistatinsajkandl AT myersandrewg synthesisofcortistatinsajkandl |