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Pyrrole-2-carboxaldehydes: Origins and Physiological Activities

Pyrrole-2-carboxaldehyde (Py-2-C) derivatives have been isolated from many natural sources, including fungi, plants (roots, leaves, and seeds), and microorganisms. The well-known diabetes molecular marker, pyrraline, which is produced after sequential reactions in vivo, has a Py-2-C skeleton. Py-2-C...

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Detalles Bibliográficos
Autores principales: Matsugo, Seiichi, Nakamura, Yutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10058459/
https://www.ncbi.nlm.nih.gov/pubmed/36985566
http://dx.doi.org/10.3390/molecules28062599
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author Matsugo, Seiichi
Nakamura, Yutaka
author_facet Matsugo, Seiichi
Nakamura, Yutaka
author_sort Matsugo, Seiichi
collection PubMed
description Pyrrole-2-carboxaldehyde (Py-2-C) derivatives have been isolated from many natural sources, including fungi, plants (roots, leaves, and seeds), and microorganisms. The well-known diabetes molecular marker, pyrraline, which is produced after sequential reactions in vivo, has a Py-2-C skeleton. Py-2-Cs can be chemically produced by the strong acid-catalyzed condensation of glucose and amino acid derivatives in vitro. These observations indicate the importance of the Py-2-C skeleton in vivo and suggest that molecules containing this skeleton have various biological functions. In this review, we have summarized Py-2-C derivatives based on their origins. We also discuss the structural characteristics, natural sources, and physiological activities of isolated compounds containing the Py-2-C group.
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spelling pubmed-100584592023-03-30 Pyrrole-2-carboxaldehydes: Origins and Physiological Activities Matsugo, Seiichi Nakamura, Yutaka Molecules Review Pyrrole-2-carboxaldehyde (Py-2-C) derivatives have been isolated from many natural sources, including fungi, plants (roots, leaves, and seeds), and microorganisms. The well-known diabetes molecular marker, pyrraline, which is produced after sequential reactions in vivo, has a Py-2-C skeleton. Py-2-Cs can be chemically produced by the strong acid-catalyzed condensation of glucose and amino acid derivatives in vitro. These observations indicate the importance of the Py-2-C skeleton in vivo and suggest that molecules containing this skeleton have various biological functions. In this review, we have summarized Py-2-C derivatives based on their origins. We also discuss the structural characteristics, natural sources, and physiological activities of isolated compounds containing the Py-2-C group. MDPI 2023-03-13 /pmc/articles/PMC10058459/ /pubmed/36985566 http://dx.doi.org/10.3390/molecules28062599 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Matsugo, Seiichi
Nakamura, Yutaka
Pyrrole-2-carboxaldehydes: Origins and Physiological Activities
title Pyrrole-2-carboxaldehydes: Origins and Physiological Activities
title_full Pyrrole-2-carboxaldehydes: Origins and Physiological Activities
title_fullStr Pyrrole-2-carboxaldehydes: Origins and Physiological Activities
title_full_unstemmed Pyrrole-2-carboxaldehydes: Origins and Physiological Activities
title_short Pyrrole-2-carboxaldehydes: Origins and Physiological Activities
title_sort pyrrole-2-carboxaldehydes: origins and physiological activities
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10058459/
https://www.ncbi.nlm.nih.gov/pubmed/36985566
http://dx.doi.org/10.3390/molecules28062599
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