Target intelligence / Profile preview

Phosphodiesterase 7 (PDE7)

Target
PDE7
Molecular classification
Enzyme, Phosphodiesterase
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Overview

Phosphodiesterase 7 (PDE7) is a member of the phosphodiesterase superfamily that specifically hydrolyzes cyclic adenosine monophosphate (cAMP), playing a crucial role in regulating intracellular cAMP signaling pathways. It exists as two main isoforms, PDE7A and PDE7B, with various splice variants. PDE7 is predominantly found in the central nervous system (CNS) and immune cells. By regulating cAMP levels, PDE7 impacts T cell activation, neurogenesis, synaptogenesis, and memory formation. Increased expression or activity of PDE7 has been implicated in several diseases, including Parkinson’s disease, Alzheimer’s disease, multiple sclerosis and various cancers, making it an attractive drug target, particularly for CNS disorders and inflammatory diseases. Common inhibitors include IBMX and papaverine, but isozyme-selective inhibitors are under development.

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Mechanism of action

Inhibition of cAMP hydrolysis

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Biological functions

Regulation of cAMP levelsSignal transductionRegulation of T cell functionNeurogenesisSynaptogenesisMemory formation
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Disease associations

Parkinson’s diseaseAlzheimer’s diseaseHuntington’s diseaseMultiple sclerosisChronic obstructive pulmonary disease (COPD)Cancer
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Safety considerations

Potential off-target effects due to non-selective inhibitorsDevelopment of isozyme-selective inhibitors needed to minimize adverse reactions
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Interacting drugs

IBMX (3-isobutyl-1-methylxanthine)

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