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Amaryllidaceae Alkaloids as Potential Glycogen Synthase Kinase-3β Inhibitors
Glycogen synthase kinase-3β (GSK-3β) is a multifunctional serine/threonine protein kinase that was originally identified as an enzyme involved in the control of glycogen metabolism. It plays a key role in diverse physiological processes including metabolism, the cell cycle, and gene expression by re...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017564/ https://www.ncbi.nlm.nih.gov/pubmed/29561817 http://dx.doi.org/10.3390/molecules23040719 |
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author | Hulcová, Daniela Breiterová, Kateřina Siatka, Tomáš Klímová, Kamila Davani, Lara Šafratová, Marcela Hošťálková, Anna De Simone, Angela Andrisano, Vincenza Cahlíková, Lucie |
author_facet | Hulcová, Daniela Breiterová, Kateřina Siatka, Tomáš Klímová, Kamila Davani, Lara Šafratová, Marcela Hošťálková, Anna De Simone, Angela Andrisano, Vincenza Cahlíková, Lucie |
author_sort | Hulcová, Daniela |
collection | PubMed |
description | Glycogen synthase kinase-3β (GSK-3β) is a multifunctional serine/threonine protein kinase that was originally identified as an enzyme involved in the control of glycogen metabolism. It plays a key role in diverse physiological processes including metabolism, the cell cycle, and gene expression by regulating a wide variety of well-known substances like glycogen synthase, tau-protein, and β-catenin. Recent studies have identified GSK-3β as a potential therapeutic target in Alzheimer´s disease, bipolar disorder, stroke, more than 15 types of cancer, and diabetes. GSK-3β is one of the most attractive targets for medicinal chemists in the discovery, design, and synthesis of new selective potent inhibitors. In the current study, twenty-eight Amaryllidaceae alkaloids of various structural types were studied for their potency to inhibit GSK-3β. Promising results have been demonstrated by alkaloids of the homolycorine-{9-O-demethylhomolycorine (IC(50) = 30.00 ± 0.71 µM), masonine (IC(50) = 27.81 ± 0.01 μM)}, and lycorine-types {caranine (IC(50) = 30.75 ± 0.04 μM)}. |
format | Online Article Text |
id | pubmed-6017564 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60175642018-11-13 Amaryllidaceae Alkaloids as Potential Glycogen Synthase Kinase-3β Inhibitors Hulcová, Daniela Breiterová, Kateřina Siatka, Tomáš Klímová, Kamila Davani, Lara Šafratová, Marcela Hošťálková, Anna De Simone, Angela Andrisano, Vincenza Cahlíková, Lucie Molecules Article Glycogen synthase kinase-3β (GSK-3β) is a multifunctional serine/threonine protein kinase that was originally identified as an enzyme involved in the control of glycogen metabolism. It plays a key role in diverse physiological processes including metabolism, the cell cycle, and gene expression by regulating a wide variety of well-known substances like glycogen synthase, tau-protein, and β-catenin. Recent studies have identified GSK-3β as a potential therapeutic target in Alzheimer´s disease, bipolar disorder, stroke, more than 15 types of cancer, and diabetes. GSK-3β is one of the most attractive targets for medicinal chemists in the discovery, design, and synthesis of new selective potent inhibitors. In the current study, twenty-eight Amaryllidaceae alkaloids of various structural types were studied for their potency to inhibit GSK-3β. Promising results have been demonstrated by alkaloids of the homolycorine-{9-O-demethylhomolycorine (IC(50) = 30.00 ± 0.71 µM), masonine (IC(50) = 27.81 ± 0.01 μM)}, and lycorine-types {caranine (IC(50) = 30.75 ± 0.04 μM)}. MDPI 2018-03-21 /pmc/articles/PMC6017564/ /pubmed/29561817 http://dx.doi.org/10.3390/molecules23040719 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hulcová, Daniela Breiterová, Kateřina Siatka, Tomáš Klímová, Kamila Davani, Lara Šafratová, Marcela Hošťálková, Anna De Simone, Angela Andrisano, Vincenza Cahlíková, Lucie Amaryllidaceae Alkaloids as Potential Glycogen Synthase Kinase-3β Inhibitors |
title | Amaryllidaceae Alkaloids as Potential Glycogen Synthase Kinase-3β Inhibitors |
title_full | Amaryllidaceae Alkaloids as Potential Glycogen Synthase Kinase-3β Inhibitors |
title_fullStr | Amaryllidaceae Alkaloids as Potential Glycogen Synthase Kinase-3β Inhibitors |
title_full_unstemmed | Amaryllidaceae Alkaloids as Potential Glycogen Synthase Kinase-3β Inhibitors |
title_short | Amaryllidaceae Alkaloids as Potential Glycogen Synthase Kinase-3β Inhibitors |
title_sort | amaryllidaceae alkaloids as potential glycogen synthase kinase-3β inhibitors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017564/ https://www.ncbi.nlm.nih.gov/pubmed/29561817 http://dx.doi.org/10.3390/molecules23040719 |
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