PDE4D: A Multipurpose Pharmacological Target.
catechol moiety
drug design
neurodegenerative diseases
phosphodiesterases 4
phosphodiesterases 4D
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
24 Jul 2024
24 Jul 2024
Historique:
received:
26
06
2024
revised:
18
07
2024
accepted:
22
07
2024
medline:
10
8
2024
pubmed:
10
8
2024
entrez:
10
8
2024
Statut:
epublish
Résumé
Phosphodiesterase 4 (PDE4) enzymes catalyze cyclic adenosine monophosphate (cAMP) hydrolysis and are involved in a variety of physiological processes, including brain function, monocyte and macrophage activation, and neutrophil infiltration. Among different PDE4 isoforms, Phosphodiesterases 4D (PDE4Ds) play a fundamental role in cognitive, learning and memory consolidation processes and cancer development. Selective PDE4D inhibitors (PDE4Dis) could represent an innovative and valid therapeutic strategy for the treatment of various neurodegenerative diseases, such as Alzheimer's, Parkinson's, Huntington's, and Lou Gehrig's diseases, but also for stroke, traumatic brain and spinal cord injury, mild cognitive impairment, and all demyelinating diseases such as multiple sclerosis. In addition, small molecules able to block PDE4D isoforms have been recently studied for the treatment of specific cancer types, particularly hepatocellular carcinoma and breast cancer. This review overviews the PDE4DIsso far identified and provides useful information, from a medicinal chemistry point of view, for the development of a novel series of compounds with improved pharmacological properties.
Identifiants
pubmed: 39125619
pii: ijms25158052
doi: 10.3390/ijms25158052
pii:
doi:
Substances chimiques
Cyclic Nucleotide Phosphodiesterases, Type 4
EC 3.1.4.17
Phosphodiesterase 4 Inhibitors
0
PDE4D protein, human
EC 3.1.4.17
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM