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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
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.
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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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