Design and synthesis of novel imidazo[1,2- a ]quinoxalines as PDE4 inhibitors-Reference-Cited by-同舟云学术

Design and synthesis of novel imidazo[1,2- a ]quinoxalines as PDE4 inhibitors

Published:2004-03 Issue:5 Volume:12 Page:1129-1139
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Deleuze-Masquéfa Carine,Gerebtzoff Grégori,Subra Guy,Fabreguettes Jean-Roch,Ovens Annabel,Carraz Maëlle,Strub Marie-Paule,Bompart Jacques,George Pascal,Bonnet Pierre-Antoine

Publisher

Elsevier BV

Subject

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

Reference17 articles.

1. Phosphodiesterase 4 inhibitors, structurally unrelated to Rolipram, as promising agents for the treatment of asthma and other pathologies

2. Cloning and characterization of a cAMP-specific cyclic nucleotide phosphodiesterase

3. Cyclic AMP-specific PDE4 Phosphodiesterases as Critical Components of Cyclic AMP Signaling

4. PDE4 cAMP phosphodiesterases: modular enzymes that orchestrate signalling cross-talk, desensitization and compartmentalization

5. Immunosuppressive and anti-inflammatory effects of cyclic AMP phosphodiesterase (PDE) type 4 inhibitors

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