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First Optimization of Novel, Potent, Selective PDE11A4 Inhibitors for Age-Related Cognitive Decline
[Image: see text] Phosphodiesterase 11A4 (PDE11A4) is a dual-acting cyclic nucleotide hydrolase expressed in neurons in the CA1, subiculum, amygdalostriatal transition area and amygdalohippocampal area of the extended hippocampal formation. PDE11A4 is the only PDE enzyme to emanate solely from hippo...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10641827/ https://www.ncbi.nlm.nih.gov/pubmed/37862143 http://dx.doi.org/10.1021/acs.jmedchem.3c01088 |
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author | Mahmood, Shams ul Lozano Gonzalez, Mariana Tummalapalli, Sreedhar Eberhard, Jeremy Ly, Judy Hoffman, Charles S. Kelly, Michy P. Gordon, John Colussi, Dennis Childers, Wayne Rotella, David P. |
author_facet | Mahmood, Shams ul Lozano Gonzalez, Mariana Tummalapalli, Sreedhar Eberhard, Jeremy Ly, Judy Hoffman, Charles S. Kelly, Michy P. Gordon, John Colussi, Dennis Childers, Wayne Rotella, David P. |
author_sort | Mahmood, Shams ul |
collection | PubMed |
description | [Image: see text] Phosphodiesterase 11A4 (PDE11A4) is a dual-acting cyclic nucleotide hydrolase expressed in neurons in the CA1, subiculum, amygdalostriatal transition area and amygdalohippocampal area of the extended hippocampal formation. PDE11A4 is the only PDE enzyme to emanate solely from hippocampal formation, a key brain region for the formation of long-term memory. PDE11A4 expression increases in the hippocampal formation of both humans and rodents as they age. Interestingly, PDE11A knockout mice do not show age-related deficits in associative memory and show no gross histopathology. This suggests that inhibition of PDE11A4 might serve as a therapeutic option for age-related cognitive decline. A novel, yeast-based high throughput screen previously identified moderately potent, selective PDE11A4 inhibitors, and this work describes initial efforts that improved potency more than 10-fold and improved some pharmaceutical properties of one of these scaffolds, leading to selective, cell-penetrant PDE11A4 inhibitors, one of which is 10-fold more potent compared to tadalafil in cell-based activity. |
format | Online Article Text |
id | pubmed-10641827 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-106418272023-11-15 First Optimization of Novel, Potent, Selective PDE11A4 Inhibitors for Age-Related Cognitive Decline Mahmood, Shams ul Lozano Gonzalez, Mariana Tummalapalli, Sreedhar Eberhard, Jeremy Ly, Judy Hoffman, Charles S. Kelly, Michy P. Gordon, John Colussi, Dennis Childers, Wayne Rotella, David P. J Med Chem [Image: see text] Phosphodiesterase 11A4 (PDE11A4) is a dual-acting cyclic nucleotide hydrolase expressed in neurons in the CA1, subiculum, amygdalostriatal transition area and amygdalohippocampal area of the extended hippocampal formation. PDE11A4 is the only PDE enzyme to emanate solely from hippocampal formation, a key brain region for the formation of long-term memory. PDE11A4 expression increases in the hippocampal formation of both humans and rodents as they age. Interestingly, PDE11A knockout mice do not show age-related deficits in associative memory and show no gross histopathology. This suggests that inhibition of PDE11A4 might serve as a therapeutic option for age-related cognitive decline. A novel, yeast-based high throughput screen previously identified moderately potent, selective PDE11A4 inhibitors, and this work describes initial efforts that improved potency more than 10-fold and improved some pharmaceutical properties of one of these scaffolds, leading to selective, cell-penetrant PDE11A4 inhibitors, one of which is 10-fold more potent compared to tadalafil in cell-based activity. American Chemical Society 2023-10-20 /pmc/articles/PMC10641827/ /pubmed/37862143 http://dx.doi.org/10.1021/acs.jmedchem.3c01088 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Mahmood, Shams ul Lozano Gonzalez, Mariana Tummalapalli, Sreedhar Eberhard, Jeremy Ly, Judy Hoffman, Charles S. Kelly, Michy P. Gordon, John Colussi, Dennis Childers, Wayne Rotella, David P. First Optimization of Novel, Potent, Selective PDE11A4 Inhibitors for Age-Related Cognitive Decline |
title | First Optimization
of Novel, Potent, Selective PDE11A4
Inhibitors for Age-Related Cognitive Decline |
title_full | First Optimization
of Novel, Potent, Selective PDE11A4
Inhibitors for Age-Related Cognitive Decline |
title_fullStr | First Optimization
of Novel, Potent, Selective PDE11A4
Inhibitors for Age-Related Cognitive Decline |
title_full_unstemmed | First Optimization
of Novel, Potent, Selective PDE11A4
Inhibitors for Age-Related Cognitive Decline |
title_short | First Optimization
of Novel, Potent, Selective PDE11A4
Inhibitors for Age-Related Cognitive Decline |
title_sort | first optimization
of novel, potent, selective pde11a4
inhibitors for age-related cognitive decline |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10641827/ https://www.ncbi.nlm.nih.gov/pubmed/37862143 http://dx.doi.org/10.1021/acs.jmedchem.3c01088 |
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