TY - JOUR
T1 - First Optimization of Novel, Potent, Selective PDE11A4 Inhibitors for Age-Related Cognitive Decline
AU - Mahmood, Shams ul
AU - Lozano Gonzalez, Mariana
AU - Tummalapalli, Sreedhar
AU - Eberhard, Jeremy
AU - Ly, Judy
AU - Hoffman, Charles S.
AU - Kelly, Michy P.
AU - Gordon, John
AU - Colussi, Dennis
AU - Childers, Wayne
AU - Rotella, David P.
N1 - Publisher Copyright:
© 2023 The Authors. Published by American Chemical Society
PY - 2023/11/9
Y1 - 2023/11/9
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85176509784&partnerID=8YFLogxK
U2 - 10.1021/acs.jmedchem.3c01088
DO - 10.1021/acs.jmedchem.3c01088
M3 - Article
C2 - 37862143
AN - SCOPUS:85176509784
SN - 0022-2623
VL - 66
SP - 14597
EP - 14608
JO - Journal of Medicinal Chemistry
JF - Journal of Medicinal Chemistry
IS - 21
ER -