TRR469, a potent A1 adenosine receptor allosteric modulator, exhibits anti-nociceptive properties in acute and neuropathic pain models in mice-Reference-Cited by-同舟云学术

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TRR469, a potent A1 adenosine receptor allosteric modulator, exhibits anti-nociceptive properties in acute and neuropathic pain models in mice

Published:2014-06 Issue: Volume:81 Page:6-14
ISSN:0028-3908
Container-title:Neuropharmacology
language:en
Short-container-title:Neuropharmacology

Author:

Vincenzi Fabrizio,Targa Martina,Romagnoli Romeo,Merighi Stefania,Gessi Stefania,Baraldi Pier Giovanni,Borea Pier Andrea,Varani Katia

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Pharmacology

Reference57 articles.

1. The formalin test: scoring properties of the first and second phases of the pain response in rats;Abbott;Pain,1995

2. Glutamate-evoked release of adenosine and regulation of peripheral nociception;Aumeerally;Neuroscience,2004

3. Synthesis and biological effects of a new series of 2-amino-3-benzoylthiophenes as allosteric enhancers of A1 adenosine receptor;Baraldi;Bioorg. Med. Chem. Lett.,2000

4. Synthesis and biological effects of novel 2-amino-3-naphthoylthiophenes as allosteric enhancers of the A1 adenosine receptor;Baraldi;J. Med. Chem.,2003

5. Synthesis of 2-amino-3-heteroaroylthiophenes and evaluation of their activity as potential allosteric enhancers at the human A1 receptor;Baraldi;Eur. J. Med. Chem.,2004

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