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The Hantzsch reaction for nitrogen-13 PET: preparation of [(13)N]nifedipine and derivatives
Nitrogen-13 is an attractive but under-used PET radionuclide for labelling molecules of biological and pharmaceutical interest, complementing other PET radionuclides. Its short half-life (t(1/2) = 9.97 min) imposes synthetic challenges, but we have expanded the hitherto limited pool of (13)N labelli...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8132178/ https://www.ncbi.nlm.nih.gov/pubmed/33876157 http://dx.doi.org/10.1039/d1cc00495f |
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author | Blower, Julia E. Ma, Michelle T. Al-Salemee, Fahad A. I. Gee, Antony D. |
author_facet | Blower, Julia E. Ma, Michelle T. Al-Salemee, Fahad A. I. Gee, Antony D. |
author_sort | Blower, Julia E. |
collection | PubMed |
description | Nitrogen-13 is an attractive but under-used PET radionuclide for labelling molecules of biological and pharmaceutical interest, complementing other PET radionuclides. Its short half-life (t(1/2) = 9.97 min) imposes synthetic challenges, but we have expanded the hitherto limited pool of (13)N labelling strategies and tracers by adapting the multicomponent Hantzsch condensation reaction to prepare a library of (13)N-labelled 1,4-dihydropyridines from [(13)N]ammonia, including the widely-used drug nifedipine. This represents a key advance in (13)N PET radiochemistry, and will serve to underpin the renewed interest in clinical opportunities offered by short-lived PET tracers. |
format | Online Article Text |
id | pubmed-8132178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-81321782021-05-25 The Hantzsch reaction for nitrogen-13 PET: preparation of [(13)N]nifedipine and derivatives Blower, Julia E. Ma, Michelle T. Al-Salemee, Fahad A. I. Gee, Antony D. Chem Commun (Camb) Chemistry Nitrogen-13 is an attractive but under-used PET radionuclide for labelling molecules of biological and pharmaceutical interest, complementing other PET radionuclides. Its short half-life (t(1/2) = 9.97 min) imposes synthetic challenges, but we have expanded the hitherto limited pool of (13)N labelling strategies and tracers by adapting the multicomponent Hantzsch condensation reaction to prepare a library of (13)N-labelled 1,4-dihydropyridines from [(13)N]ammonia, including the widely-used drug nifedipine. This represents a key advance in (13)N PET radiochemistry, and will serve to underpin the renewed interest in clinical opportunities offered by short-lived PET tracers. The Royal Society of Chemistry 2021-04-08 /pmc/articles/PMC8132178/ /pubmed/33876157 http://dx.doi.org/10.1039/d1cc00495f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Blower, Julia E. Ma, Michelle T. Al-Salemee, Fahad A. I. Gee, Antony D. The Hantzsch reaction for nitrogen-13 PET: preparation of [(13)N]nifedipine and derivatives |
title | The Hantzsch reaction for nitrogen-13 PET: preparation of [(13)N]nifedipine and derivatives |
title_full | The Hantzsch reaction for nitrogen-13 PET: preparation of [(13)N]nifedipine and derivatives |
title_fullStr | The Hantzsch reaction for nitrogen-13 PET: preparation of [(13)N]nifedipine and derivatives |
title_full_unstemmed | The Hantzsch reaction for nitrogen-13 PET: preparation of [(13)N]nifedipine and derivatives |
title_short | The Hantzsch reaction for nitrogen-13 PET: preparation of [(13)N]nifedipine and derivatives |
title_sort | hantzsch reaction for nitrogen-13 pet: preparation of [(13)n]nifedipine and derivatives |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8132178/ https://www.ncbi.nlm.nih.gov/pubmed/33876157 http://dx.doi.org/10.1039/d1cc00495f |
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