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Small Molecule Inhibitors of DYRK1A Identified by Computational and Experimental Approaches

Dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) is a protein kinase with diverse functions in cell regulation. Abnormal expression and activity of DYRK1A contribute to numerous human malignancies, Down syndrome, and Alzheimer’s disease. Notably, DYRK1A has been proposed as a p...

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Detalles Bibliográficos
Autores principales: Yoon, Hye Ree, Balupuri, Anand, Choi, Kwang-Eun, Kang, Nam Sook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7554884/
https://www.ncbi.nlm.nih.gov/pubmed/32957634
http://dx.doi.org/10.3390/ijms21186826
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author Yoon, Hye Ree
Balupuri, Anand
Choi, Kwang-Eun
Kang, Nam Sook
author_facet Yoon, Hye Ree
Balupuri, Anand
Choi, Kwang-Eun
Kang, Nam Sook
author_sort Yoon, Hye Ree
collection PubMed
description Dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) is a protein kinase with diverse functions in cell regulation. Abnormal expression and activity of DYRK1A contribute to numerous human malignancies, Down syndrome, and Alzheimer’s disease. Notably, DYRK1A has been proposed as a potential therapeutic target for the treatment of diabetes because of its key role in pancreatic β-cell proliferation. Consequently, DYRK1A is an attractive drug target for a variety of diseases. Here, we report the identification of several DYRK1A inhibitors using our in-house topological water network-based approach. All inhibitors were further verified by in vitro assay.
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spelling pubmed-75548842020-10-14 Small Molecule Inhibitors of DYRK1A Identified by Computational and Experimental Approaches Yoon, Hye Ree Balupuri, Anand Choi, Kwang-Eun Kang, Nam Sook Int J Mol Sci Article Dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) is a protein kinase with diverse functions in cell regulation. Abnormal expression and activity of DYRK1A contribute to numerous human malignancies, Down syndrome, and Alzheimer’s disease. Notably, DYRK1A has been proposed as a potential therapeutic target for the treatment of diabetes because of its key role in pancreatic β-cell proliferation. Consequently, DYRK1A is an attractive drug target for a variety of diseases. Here, we report the identification of several DYRK1A inhibitors using our in-house topological water network-based approach. All inhibitors were further verified by in vitro assay. MDPI 2020-09-17 /pmc/articles/PMC7554884/ /pubmed/32957634 http://dx.doi.org/10.3390/ijms21186826 Text en © 2020 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
Yoon, Hye Ree
Balupuri, Anand
Choi, Kwang-Eun
Kang, Nam Sook
Small Molecule Inhibitors of DYRK1A Identified by Computational and Experimental Approaches
title Small Molecule Inhibitors of DYRK1A Identified by Computational and Experimental Approaches
title_full Small Molecule Inhibitors of DYRK1A Identified by Computational and Experimental Approaches
title_fullStr Small Molecule Inhibitors of DYRK1A Identified by Computational and Experimental Approaches
title_full_unstemmed Small Molecule Inhibitors of DYRK1A Identified by Computational and Experimental Approaches
title_short Small Molecule Inhibitors of DYRK1A Identified by Computational and Experimental Approaches
title_sort small molecule inhibitors of dyrk1a identified by computational and experimental approaches
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7554884/
https://www.ncbi.nlm.nih.gov/pubmed/32957634
http://dx.doi.org/10.3390/ijms21186826
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