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Suzuki coupling-based synthesis of VATPase inhibitor archazolid natural product derived fragments
An archazolid natural product fragment that displays dose-dependent inhibition of the vacuolar-type ATPase (VATPase) has been synthesized by a high-yielding Suzuki coupling of two complex subunits. Similarly, a further simplified fragment was prepared and evaluated for VATPase inhibitory activity. T...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072946/ https://www.ncbi.nlm.nih.gov/pubmed/35530773 http://dx.doi.org/10.1039/c9ra07050h |
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author | Vincent, Cooper T. Long, Evan T. Jones, Holly C. Young, Jeffrey C. Spiegel, P. Clint O'Neil, Gregory W. |
author_facet | Vincent, Cooper T. Long, Evan T. Jones, Holly C. Young, Jeffrey C. Spiegel, P. Clint O'Neil, Gregory W. |
author_sort | Vincent, Cooper T. |
collection | PubMed |
description | An archazolid natural product fragment that displays dose-dependent inhibition of the vacuolar-type ATPase (VATPase) has been synthesized by a high-yielding Suzuki coupling of two complex subunits. Similarly, a further simplified fragment was prepared and evaluated for VATPase inhibitory activity. This compound did inhibit the VATPase, as evidenced by growth inhibition of etiolated Arabidopsis seedlings, however at approximately 10× lower potency than the more complex fragment. Cyclooxygenase (COX) enzyme inhibition was not observed for either fragment. |
format | Online Article Text |
id | pubmed-9072946 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90729462022-05-06 Suzuki coupling-based synthesis of VATPase inhibitor archazolid natural product derived fragments Vincent, Cooper T. Long, Evan T. Jones, Holly C. Young, Jeffrey C. Spiegel, P. Clint O'Neil, Gregory W. RSC Adv Chemistry An archazolid natural product fragment that displays dose-dependent inhibition of the vacuolar-type ATPase (VATPase) has been synthesized by a high-yielding Suzuki coupling of two complex subunits. Similarly, a further simplified fragment was prepared and evaluated for VATPase inhibitory activity. This compound did inhibit the VATPase, as evidenced by growth inhibition of etiolated Arabidopsis seedlings, however at approximately 10× lower potency than the more complex fragment. Cyclooxygenase (COX) enzyme inhibition was not observed for either fragment. The Royal Society of Chemistry 2019-10-10 /pmc/articles/PMC9072946/ /pubmed/35530773 http://dx.doi.org/10.1039/c9ra07050h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Vincent, Cooper T. Long, Evan T. Jones, Holly C. Young, Jeffrey C. Spiegel, P. Clint O'Neil, Gregory W. Suzuki coupling-based synthesis of VATPase inhibitor archazolid natural product derived fragments |
title | Suzuki coupling-based synthesis of VATPase inhibitor archazolid natural product derived fragments |
title_full | Suzuki coupling-based synthesis of VATPase inhibitor archazolid natural product derived fragments |
title_fullStr | Suzuki coupling-based synthesis of VATPase inhibitor archazolid natural product derived fragments |
title_full_unstemmed | Suzuki coupling-based synthesis of VATPase inhibitor archazolid natural product derived fragments |
title_short | Suzuki coupling-based synthesis of VATPase inhibitor archazolid natural product derived fragments |
title_sort | suzuki coupling-based synthesis of vatpase inhibitor archazolid natural product derived fragments |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072946/ https://www.ncbi.nlm.nih.gov/pubmed/35530773 http://dx.doi.org/10.1039/c9ra07050h |
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