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Concise synthesis of artemisinin from a farnesyl diphosphate analogue

Artemisinin is one of the most potent anti-malaria drugs and many often-lengthy routes have been developed for its synthesis. Amorphadiene synthase, a key enzyme in the biosynthetic pathway of artemisinin, is able to convert an oxygenated farnesyl diphosphate analogue directly to dihydroartemisinic...

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Detalles Bibliográficos
Autores principales: Tang, Xiaoping, Demiray, Melodi, Wirth, Thomas, Allemann, Rudolf K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930831/
https://www.ncbi.nlm.nih.gov/pubmed/28404524
http://dx.doi.org/10.1016/j.bmc.2017.03.068
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author Tang, Xiaoping
Demiray, Melodi
Wirth, Thomas
Allemann, Rudolf K.
author_facet Tang, Xiaoping
Demiray, Melodi
Wirth, Thomas
Allemann, Rudolf K.
author_sort Tang, Xiaoping
collection PubMed
description Artemisinin is one of the most potent anti-malaria drugs and many often-lengthy routes have been developed for its synthesis. Amorphadiene synthase, a key enzyme in the biosynthetic pathway of artemisinin, is able to convert an oxygenated farnesyl diphosphate analogue directly to dihydroartemisinic aldehyde, which can be converted to artemisinin in only four chemical steps, resulting in an efficient synthetic route to the anti-malaria drug.
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spelling pubmed-59308312018-05-03 Concise synthesis of artemisinin from a farnesyl diphosphate analogue Tang, Xiaoping Demiray, Melodi Wirth, Thomas Allemann, Rudolf K. Bioorg Med Chem Article Artemisinin is one of the most potent anti-malaria drugs and many often-lengthy routes have been developed for its synthesis. Amorphadiene synthase, a key enzyme in the biosynthetic pathway of artemisinin, is able to convert an oxygenated farnesyl diphosphate analogue directly to dihydroartemisinic aldehyde, which can be converted to artemisinin in only four chemical steps, resulting in an efficient synthetic route to the anti-malaria drug. Elsevier Science 2018-04-01 /pmc/articles/PMC5930831/ /pubmed/28404524 http://dx.doi.org/10.1016/j.bmc.2017.03.068 Text en © 2017 The Authors. Published by Elsevier Ltd. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tang, Xiaoping
Demiray, Melodi
Wirth, Thomas
Allemann, Rudolf K.
Concise synthesis of artemisinin from a farnesyl diphosphate analogue
title Concise synthesis of artemisinin from a farnesyl diphosphate analogue
title_full Concise synthesis of artemisinin from a farnesyl diphosphate analogue
title_fullStr Concise synthesis of artemisinin from a farnesyl diphosphate analogue
title_full_unstemmed Concise synthesis of artemisinin from a farnesyl diphosphate analogue
title_short Concise synthesis of artemisinin from a farnesyl diphosphate analogue
title_sort concise synthesis of artemisinin from a farnesyl diphosphate analogue
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930831/
https://www.ncbi.nlm.nih.gov/pubmed/28404524
http://dx.doi.org/10.1016/j.bmc.2017.03.068
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