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In Depth Analysis of Kinase Cross Screening Data to Identify CAMKK2 Inhibitory Scaffolds
The calcium/calmodulin-dependent protein kinase kinase 2 (CAMKK2) activates CAMK1, CAMK4, AMPK, and AKT, leading to numerous physiological responses. The deregulation of CAMKK2 is linked to several diseases, suggesting the utility of CAMKK2 inhibitors for oncological, metabolic and inflammatory indi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7024175/ https://www.ncbi.nlm.nih.gov/pubmed/31941153 http://dx.doi.org/10.3390/molecules25020325 |
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author | O’Byrne, Sean N. Scott, John W. Pilotte, Joseph R. Santiago, André da S. Langendorf, Christopher G. Oakhill, Jonathan S. Eduful, Benjamin J. Couñago, Rafael M. Wells, Carrow I. Zuercher, William J. Willson, Timothy M. Drewry, David H. |
author_facet | O’Byrne, Sean N. Scott, John W. Pilotte, Joseph R. Santiago, André da S. Langendorf, Christopher G. Oakhill, Jonathan S. Eduful, Benjamin J. Couñago, Rafael M. Wells, Carrow I. Zuercher, William J. Willson, Timothy M. Drewry, David H. |
author_sort | O’Byrne, Sean N. |
collection | PubMed |
description | The calcium/calmodulin-dependent protein kinase kinase 2 (CAMKK2) activates CAMK1, CAMK4, AMPK, and AKT, leading to numerous physiological responses. The deregulation of CAMKK2 is linked to several diseases, suggesting the utility of CAMKK2 inhibitors for oncological, metabolic and inflammatory indications. In this work, we demonstrate that STO-609, frequently described as a selective inhibitor for CAMKK2, potently inhibits a significant number of other kinases. Through an analysis of literature and public databases, we have identified other potent CAMKK2 inhibitors and verified their activities in differential scanning fluorimetry and enzyme inhibition assays. These inhibitors are potential starting points for the development of selective CAMKK2 inhibitors and will lead to tools that delineate the roles of this kinase in disease biology. |
format | Online Article Text |
id | pubmed-7024175 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70241752020-03-19 In Depth Analysis of Kinase Cross Screening Data to Identify CAMKK2 Inhibitory Scaffolds O’Byrne, Sean N. Scott, John W. Pilotte, Joseph R. Santiago, André da S. Langendorf, Christopher G. Oakhill, Jonathan S. Eduful, Benjamin J. Couñago, Rafael M. Wells, Carrow I. Zuercher, William J. Willson, Timothy M. Drewry, David H. Molecules Article The calcium/calmodulin-dependent protein kinase kinase 2 (CAMKK2) activates CAMK1, CAMK4, AMPK, and AKT, leading to numerous physiological responses. The deregulation of CAMKK2 is linked to several diseases, suggesting the utility of CAMKK2 inhibitors for oncological, metabolic and inflammatory indications. In this work, we demonstrate that STO-609, frequently described as a selective inhibitor for CAMKK2, potently inhibits a significant number of other kinases. Through an analysis of literature and public databases, we have identified other potent CAMKK2 inhibitors and verified their activities in differential scanning fluorimetry and enzyme inhibition assays. These inhibitors are potential starting points for the development of selective CAMKK2 inhibitors and will lead to tools that delineate the roles of this kinase in disease biology. MDPI 2020-01-13 /pmc/articles/PMC7024175/ /pubmed/31941153 http://dx.doi.org/10.3390/molecules25020325 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 O’Byrne, Sean N. Scott, John W. Pilotte, Joseph R. Santiago, André da S. Langendorf, Christopher G. Oakhill, Jonathan S. Eduful, Benjamin J. Couñago, Rafael M. Wells, Carrow I. Zuercher, William J. Willson, Timothy M. Drewry, David H. In Depth Analysis of Kinase Cross Screening Data to Identify CAMKK2 Inhibitory Scaffolds |
title | In Depth Analysis of Kinase Cross Screening Data to Identify CAMKK2 Inhibitory Scaffolds |
title_full | In Depth Analysis of Kinase Cross Screening Data to Identify CAMKK2 Inhibitory Scaffolds |
title_fullStr | In Depth Analysis of Kinase Cross Screening Data to Identify CAMKK2 Inhibitory Scaffolds |
title_full_unstemmed | In Depth Analysis of Kinase Cross Screening Data to Identify CAMKK2 Inhibitory Scaffolds |
title_short | In Depth Analysis of Kinase Cross Screening Data to Identify CAMKK2 Inhibitory Scaffolds |
title_sort | in depth analysis of kinase cross screening data to identify camkk2 inhibitory scaffolds |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7024175/ https://www.ncbi.nlm.nih.gov/pubmed/31941153 http://dx.doi.org/10.3390/molecules25020325 |
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