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Discovery of MK-8189, a Highly Potent and Selective PDE10A Inhibitor for the Treatment of Schizophrenia

[Image: see text] PDE10A is an important regulator of striatal signaling that, when inhibited, can normalize dysfunctional activity. Given the involvement of dysfunctional striatal activity with schizophrenia, PDE10A inhibition represents a potentially novel means for its treatment. With the goal of...

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Autores principales: Layton, Mark E., Kern, Jeffrey C., Hartingh, Timothy J., Shipe, William D., Raheem, Izzat, Kandebo, Monika, Hayes, Robert P., Huszar, Sarah, Eddins, Donnie, Ma, Bennett, Fuerst, Joy, Wollenberg, Gordon K., Li, Jing, Fritzen, Jeff, McGaughey, Georgia B., Uslaner, Jason M., Smith, Sean M., Coleman, Paul J., Cox, Christopher D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884086/
https://www.ncbi.nlm.nih.gov/pubmed/36624931
http://dx.doi.org/10.1021/acs.jmedchem.2c01521
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author Layton, Mark E.
Kern, Jeffrey C.
Hartingh, Timothy J.
Shipe, William D.
Raheem, Izzat
Kandebo, Monika
Hayes, Robert P.
Huszar, Sarah
Eddins, Donnie
Ma, Bennett
Fuerst, Joy
Wollenberg, Gordon K.
Li, Jing
Fritzen, Jeff
McGaughey, Georgia B.
Uslaner, Jason M.
Smith, Sean M.
Coleman, Paul J.
Cox, Christopher D.
author_facet Layton, Mark E.
Kern, Jeffrey C.
Hartingh, Timothy J.
Shipe, William D.
Raheem, Izzat
Kandebo, Monika
Hayes, Robert P.
Huszar, Sarah
Eddins, Donnie
Ma, Bennett
Fuerst, Joy
Wollenberg, Gordon K.
Li, Jing
Fritzen, Jeff
McGaughey, Georgia B.
Uslaner, Jason M.
Smith, Sean M.
Coleman, Paul J.
Cox, Christopher D.
author_sort Layton, Mark E.
collection PubMed
description [Image: see text] PDE10A is an important regulator of striatal signaling that, when inhibited, can normalize dysfunctional activity. Given the involvement of dysfunctional striatal activity with schizophrenia, PDE10A inhibition represents a potentially novel means for its treatment. With the goal of developing PDE10A inhibitors, early optimization of a fragment hit through rational design led to a series of potent pyrimidine PDE10A inhibitors that required further improvements in physicochemical properties, off-target activities, and pharmacokinetics. Herein we describe the discovery of an isomeric pyrimidine series that addresses the liabilities seen with earlier compounds and resulted in the invention of compound 18 (MK-8189), which is currently in Phase 2b clinical development for the treatment of schizophrenia.
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spelling pubmed-98840862023-01-29 Discovery of MK-8189, a Highly Potent and Selective PDE10A Inhibitor for the Treatment of Schizophrenia Layton, Mark E. Kern, Jeffrey C. Hartingh, Timothy J. Shipe, William D. Raheem, Izzat Kandebo, Monika Hayes, Robert P. Huszar, Sarah Eddins, Donnie Ma, Bennett Fuerst, Joy Wollenberg, Gordon K. Li, Jing Fritzen, Jeff McGaughey, Georgia B. Uslaner, Jason M. Smith, Sean M. Coleman, Paul J. Cox, Christopher D. J Med Chem [Image: see text] PDE10A is an important regulator of striatal signaling that, when inhibited, can normalize dysfunctional activity. Given the involvement of dysfunctional striatal activity with schizophrenia, PDE10A inhibition represents a potentially novel means for its treatment. With the goal of developing PDE10A inhibitors, early optimization of a fragment hit through rational design led to a series of potent pyrimidine PDE10A inhibitors that required further improvements in physicochemical properties, off-target activities, and pharmacokinetics. Herein we describe the discovery of an isomeric pyrimidine series that addresses the liabilities seen with earlier compounds and resulted in the invention of compound 18 (MK-8189), which is currently in Phase 2b clinical development for the treatment of schizophrenia. American Chemical Society 2023-01-10 /pmc/articles/PMC9884086/ /pubmed/36624931 http://dx.doi.org/10.1021/acs.jmedchem.2c01521 Text en © 2023 Merck & Co., Inc., Rahway, NJ, USA and its affiliates. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Layton, Mark E.
Kern, Jeffrey C.
Hartingh, Timothy J.
Shipe, William D.
Raheem, Izzat
Kandebo, Monika
Hayes, Robert P.
Huszar, Sarah
Eddins, Donnie
Ma, Bennett
Fuerst, Joy
Wollenberg, Gordon K.
Li, Jing
Fritzen, Jeff
McGaughey, Georgia B.
Uslaner, Jason M.
Smith, Sean M.
Coleman, Paul J.
Cox, Christopher D.
Discovery of MK-8189, a Highly Potent and Selective PDE10A Inhibitor for the Treatment of Schizophrenia
title Discovery of MK-8189, a Highly Potent and Selective PDE10A Inhibitor for the Treatment of Schizophrenia
title_full Discovery of MK-8189, a Highly Potent and Selective PDE10A Inhibitor for the Treatment of Schizophrenia
title_fullStr Discovery of MK-8189, a Highly Potent and Selective PDE10A Inhibitor for the Treatment of Schizophrenia
title_full_unstemmed Discovery of MK-8189, a Highly Potent and Selective PDE10A Inhibitor for the Treatment of Schizophrenia
title_short Discovery of MK-8189, a Highly Potent and Selective PDE10A Inhibitor for the Treatment of Schizophrenia
title_sort discovery of mk-8189, a highly potent and selective pde10a inhibitor for the treatment of schizophrenia
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884086/
https://www.ncbi.nlm.nih.gov/pubmed/36624931
http://dx.doi.org/10.1021/acs.jmedchem.2c01521
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