Cargando…
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...
Autores principales: | , , , |
---|---|
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 |
_version_ | 1783319548357771264 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5930831 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT tangxiaoping concisesynthesisofartemisininfromafarnesyldiphosphateanalogue AT demiraymelodi concisesynthesisofartemisininfromafarnesyldiphosphateanalogue AT wirththomas concisesynthesisofartemisininfromafarnesyldiphosphateanalogue AT allemannrudolfk concisesynthesisofartemisininfromafarnesyldiphosphateanalogue |