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Enhancement of the Click Chemistry for the Inverse Diels Alder Technology by Functionalization of Amide-Based Monomers
In the near future personalized medicine with nucleic acids will play a key role in molecular diagnostics and therapy, which require new properties of the nucleic acids, like stability against enzymatic degradation. Here we demonstrate that the replacement of nucleobases with PNA by functional molec...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3133843/ https://www.ncbi.nlm.nih.gov/pubmed/21750642 |
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author | Pipkorn, Ruediger Wiessler, Manfred Waldeck, Waldemar Lorenz, Peter Muehlhausen, Ute Fleischhacker, Heinz Koch, Mario Braun, Klaus |
author_facet | Pipkorn, Ruediger Wiessler, Manfred Waldeck, Waldemar Lorenz, Peter Muehlhausen, Ute Fleischhacker, Heinz Koch, Mario Braun, Klaus |
author_sort | Pipkorn, Ruediger |
collection | PubMed |
description | In the near future personalized medicine with nucleic acids will play a key role in molecular diagnostics and therapy, which require new properties of the nucleic acids, like stability against enzymatic degradation. Here we demonstrate that the replacement of nucleobases with PNA by functional molecules harbouring either a dienophile or a diene reactivity is feasible and confers all new options for functionalization. These newly developed derivatives allow independent multi-ligations of multi-faceted components by use of the inverse Diels Alder technology. The high chemical stability and the ease of synthesis qualify these polyamide building blocks as favourites for intracellular delivery and targeting applications. This allows local drug concentrations sufficient for imaging and therapy and simultaneously a reduction of the application doses. It is important to point out that this technology is not restricted to ligation of medicament material; it is also a candidate to develop new and highly efficient active compounds for a “sustainable pharmacy”. |
format | Online Article Text |
id | pubmed-3133843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-31338432011-07-12 Enhancement of the Click Chemistry for the Inverse Diels Alder Technology by Functionalization of Amide-Based Monomers Pipkorn, Ruediger Wiessler, Manfred Waldeck, Waldemar Lorenz, Peter Muehlhausen, Ute Fleischhacker, Heinz Koch, Mario Braun, Klaus Int J Med Sci Research Paper In the near future personalized medicine with nucleic acids will play a key role in molecular diagnostics and therapy, which require new properties of the nucleic acids, like stability against enzymatic degradation. Here we demonstrate that the replacement of nucleobases with PNA by functional molecules harbouring either a dienophile or a diene reactivity is feasible and confers all new options for functionalization. These newly developed derivatives allow independent multi-ligations of multi-faceted components by use of the inverse Diels Alder technology. The high chemical stability and the ease of synthesis qualify these polyamide building blocks as favourites for intracellular delivery and targeting applications. This allows local drug concentrations sufficient for imaging and therapy and simultaneously a reduction of the application doses. It is important to point out that this technology is not restricted to ligation of medicament material; it is also a candidate to develop new and highly efficient active compounds for a “sustainable pharmacy”. Ivyspring International Publisher 2011-06-21 /pmc/articles/PMC3133843/ /pubmed/21750642 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. |
spellingShingle | Research Paper Pipkorn, Ruediger Wiessler, Manfred Waldeck, Waldemar Lorenz, Peter Muehlhausen, Ute Fleischhacker, Heinz Koch, Mario Braun, Klaus Enhancement of the Click Chemistry for the Inverse Diels Alder Technology by Functionalization of Amide-Based Monomers |
title | Enhancement of the Click Chemistry for the Inverse Diels Alder Technology by Functionalization of Amide-Based Monomers |
title_full | Enhancement of the Click Chemistry for the Inverse Diels Alder Technology by Functionalization of Amide-Based Monomers |
title_fullStr | Enhancement of the Click Chemistry for the Inverse Diels Alder Technology by Functionalization of Amide-Based Monomers |
title_full_unstemmed | Enhancement of the Click Chemistry for the Inverse Diels Alder Technology by Functionalization of Amide-Based Monomers |
title_short | Enhancement of the Click Chemistry for the Inverse Diels Alder Technology by Functionalization of Amide-Based Monomers |
title_sort | enhancement of the click chemistry for the inverse diels alder technology by functionalization of amide-based monomers |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3133843/ https://www.ncbi.nlm.nih.gov/pubmed/21750642 |
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