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Fluorinated phenylalanines: synthesis and pharmaceutical applications

Recent advances in the chemistry of peptides containing fluorinated phenylalanines (Phe) represents a hot topic in drug research over the last few decades. ᴅ- or ʟ-fluorinated phenylalanines have had considerable industrial and pharmaceutical applications and they have been expanded also to play an...

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Autores principales: Awad, Laila Fathy, Ayoup, Mohammed Salah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7237815/
https://www.ncbi.nlm.nih.gov/pubmed/32509033
http://dx.doi.org/10.3762/bjoc.16.91
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author Awad, Laila Fathy
Ayoup, Mohammed Salah
author_facet Awad, Laila Fathy
Ayoup, Mohammed Salah
author_sort Awad, Laila Fathy
collection PubMed
description Recent advances in the chemistry of peptides containing fluorinated phenylalanines (Phe) represents a hot topic in drug research over the last few decades. ᴅ- or ʟ-fluorinated phenylalanines have had considerable industrial and pharmaceutical applications and they have been expanded also to play an important role as potential enzyme inhibitors as well as therapeutic agents and topography imaging of tumor ecosystems using PET. Incorporation of fluorinated aromatic amino acids into proteins increases their catabolic stability especially in therapeutic proteins and peptide-based vaccines. This review seeks to summarize the different synthetic approaches in the literature to prepare ᴅ- or ʟ-fluorinated phenylalanines and their pharmaceutical applications with a focus on published synthetic methods that introduce fluorine into the phenyl, the β-carbon or the α-carbon of ᴅ-or ʟ-phenylalanines.
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spelling pubmed-72378152020-06-04 Fluorinated phenylalanines: synthesis and pharmaceutical applications Awad, Laila Fathy Ayoup, Mohammed Salah Beilstein J Org Chem Review Recent advances in the chemistry of peptides containing fluorinated phenylalanines (Phe) represents a hot topic in drug research over the last few decades. ᴅ- or ʟ-fluorinated phenylalanines have had considerable industrial and pharmaceutical applications and they have been expanded also to play an important role as potential enzyme inhibitors as well as therapeutic agents and topography imaging of tumor ecosystems using PET. Incorporation of fluorinated aromatic amino acids into proteins increases their catabolic stability especially in therapeutic proteins and peptide-based vaccines. This review seeks to summarize the different synthetic approaches in the literature to prepare ᴅ- or ʟ-fluorinated phenylalanines and their pharmaceutical applications with a focus on published synthetic methods that introduce fluorine into the phenyl, the β-carbon or the α-carbon of ᴅ-or ʟ-phenylalanines. Beilstein-Institut 2020-05-15 /pmc/articles/PMC7237815/ /pubmed/32509033 http://dx.doi.org/10.3762/bjoc.16.91 Text en Copyright © 2020, Awad and Ayoup https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Review
Awad, Laila Fathy
Ayoup, Mohammed Salah
Fluorinated phenylalanines: synthesis and pharmaceutical applications
title Fluorinated phenylalanines: synthesis and pharmaceutical applications
title_full Fluorinated phenylalanines: synthesis and pharmaceutical applications
title_fullStr Fluorinated phenylalanines: synthesis and pharmaceutical applications
title_full_unstemmed Fluorinated phenylalanines: synthesis and pharmaceutical applications
title_short Fluorinated phenylalanines: synthesis and pharmaceutical applications
title_sort fluorinated phenylalanines: synthesis and pharmaceutical applications
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7237815/
https://www.ncbi.nlm.nih.gov/pubmed/32509033
http://dx.doi.org/10.3762/bjoc.16.91
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