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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...

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Detalles Bibliográficos
Autores principales: Vincent, Cooper T., Long, Evan T., Jones, Holly C., Young, Jeffrey C., Spiegel, P. Clint, O'Neil, Gregory W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
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.
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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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