Design and Synthesis of Xanthines and Cyclic GMP Analogues as Potent Inhibitors of PDE5-Reference-Cited by-同舟云学术

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Design and Synthesis of Xanthines and Cyclic GMP Analogues as Potent Inhibitors of PDE5

Published:1996 Issue: Volume: Page:135-146
ISSN:
Container-title:Phosphodiesterase Inhibitors
language:
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Author:

Sekhar Konjeti R.,Grondin Pascal,Francis Sharron H.,Corbin Jackie D.

Publisher

Elsevier

Reference37 articles.

1. Potential purine antagonists. XXXIII. Synthesis of chloropurines;Beaman;J. Appl. Chem.,1962

2. Multiple isozymes of cyclic nucleotide phosphodiesterase;Beavo;Adv. Second Messenger Phosphoprotein Res,1988

3. Multiple cyclic nucleotide phosphodiesterases;Beavo;Mol. Pharmacol.,1994

4. Discriminative insulin antagonism of stimulatory effects of various cAMP analogs on adipocyte lipolysis and hepatocyte glycogenolysis;Beebe;J. Biol. Chem.,1985

5. cAMP analogs used to study low-Km, hormone-sensitive phosphodiesterase;Beebe;Methods Enzymol.,1988

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1. Phosphodiesterase Inhibitors: Factors That Influence Potency, Selectivity, and Action;Phosphodiesterases as Drug Targets;2011

2. Phosphodiesterase 5 Inhibitors to Treat Erectile Dysfunction;Analogue-Based Drug Discovery II;2010-08-30

3. Inhibition of Cyclic Nucleotide Phosphodiesterases by Methylxanthines and Related Compounds;Methylxanthines;2010-08-19

4. cGMP-Dependent Protein Kinases and cGMP Phosphodiesterases in Nitric Oxide and cGMP Action;Pharmacological Reviews;2010-08-17

5. Cyclic GMP-Hydrolyzing Phosphodiesterases;cGMP: Generators, Effectors and Therapeutic Implications;2009

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