A new chemical tool for exploring the physiological function of the PDE2 isozyme-Reference-Cited by-同舟云学术

A new chemical tool for exploring the physiological function of the PDE2 isozyme

Published:2006-01 Issue:2 Volume:16 Page:307-310
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Chambers Robert J.,Abrams Kristin,Garceau Norman Y.,Kamath Ajith V.,Manley Christopher M.,Lilley Susan C.,Otte Douglas A.,Scott Dennis O.,Sheils Alissa L.,Tess David A.,Vellekoop A. Samuel,Zhang Yan,Lam Kelvin T.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference37 articles.

1. Cyclic GMP as substrate and regulator of cyclic nucleotide phosphodiesterases (PDEs)

2. Identification of the bioactive enantiomer of erthro-3-(adenin-9-YL)-2-nonanol (EHNA), a semi-tight binding inhibitor of adenosine deaminase

3. Isozyme selective inhibition of cGMP-stimulated cyclic nucleotide phosphodiesterases by erythro-9-(2-hydroxy-3-nonyl) adenine

4. PDE2 inhibition by the PI3 kinase inhibitor LY294002 and analogues

5. Inhibition of phosphodiesterase 2 increases neuronal cGMP, synaptic plasticity and memory performance

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