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A short and efficient total synthesis of the bromotyrosine-derived alkaloid psammaplysene A
Psammaplysene A, an inhibitor of FOXO1a-mediated nuclear export, has been synthesized by a concise and improved route from tyrosine-derived acid and amine fragments which were easily constructed using commercially available p-hydroxybenzaldehyde and tyramine as starting material, respectively. The s...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079787/ https://www.ncbi.nlm.nih.gov/pubmed/35539328 http://dx.doi.org/10.1039/c8ra02052c |
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author | Xu, Jingjing Wang, Kai Wu, Jinlong |
author_facet | Xu, Jingjing Wang, Kai Wu, Jinlong |
author_sort | Xu, Jingjing |
collection | PubMed |
description | Psammaplysene A, an inhibitor of FOXO1a-mediated nuclear export, has been synthesized by a concise and improved route from tyrosine-derived acid and amine fragments which were easily constructed using commercially available p-hydroxybenzaldehyde and tyramine as starting material, respectively. The strategy provides an efficient access of psammaplysene analogues that can be explored for potential pharmaceutical or biological activities. |
format | Online Article Text |
id | pubmed-9079787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90797872022-05-09 A short and efficient total synthesis of the bromotyrosine-derived alkaloid psammaplysene A Xu, Jingjing Wang, Kai Wu, Jinlong RSC Adv Chemistry Psammaplysene A, an inhibitor of FOXO1a-mediated nuclear export, has been synthesized by a concise and improved route from tyrosine-derived acid and amine fragments which were easily constructed using commercially available p-hydroxybenzaldehyde and tyramine as starting material, respectively. The strategy provides an efficient access of psammaplysene analogues that can be explored for potential pharmaceutical or biological activities. The Royal Society of Chemistry 2018-04-12 /pmc/articles/PMC9079787/ /pubmed/35539328 http://dx.doi.org/10.1039/c8ra02052c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Xu, Jingjing Wang, Kai Wu, Jinlong A short and efficient total synthesis of the bromotyrosine-derived alkaloid psammaplysene A |
title | A short and efficient total synthesis of the bromotyrosine-derived alkaloid psammaplysene A |
title_full | A short and efficient total synthesis of the bromotyrosine-derived alkaloid psammaplysene A |
title_fullStr | A short and efficient total synthesis of the bromotyrosine-derived alkaloid psammaplysene A |
title_full_unstemmed | A short and efficient total synthesis of the bromotyrosine-derived alkaloid psammaplysene A |
title_short | A short and efficient total synthesis of the bromotyrosine-derived alkaloid psammaplysene A |
title_sort | short and efficient total synthesis of the bromotyrosine-derived alkaloid psammaplysene a |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079787/ https://www.ncbi.nlm.nih.gov/pubmed/35539328 http://dx.doi.org/10.1039/c8ra02052c |
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