Synthesis and SAR studies of trisubstituted purinones as potent and selective adenosine A2A receptor antagonists-Reference-Cited by-同舟云学术

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Synthesis and SAR studies of trisubstituted purinones as potent and selective adenosine A2A receptor antagonists

Published:2009-03 Issue:5 Volume:19 Page:1399-1402
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Shao Yuefei,Cole Andrew G.,Brescia Marc-Raleigh,Qin Lan-Ying,Duo Jingqi,Stauffer Tara M.,Rokosz Laura L.,McGuinness Brian F.,Henderson Ian

Publisher

Elsevier BV

Subject

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

Reference16 articles.

1. The Role and Regulation of Adenosine in the Central Nervous System

2. Adenosine A2A Receptor Antagonists and Parkinsons Disease: State of the Art and Future Directions

3. Adenosine receptors

4. Internalization and desensitization of adenosine receptors

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3. Bicyclic 5-6 Systems: Purines;Comprehensive Heterocyclic Chemistry IV;2022

4. Highly Regioselective Organocatalytic SN Ar Amination of 2,4-Dichloropyrimidine and Related Heteroaryl Chlorides;European Journal of Organic Chemistry;2017-06-12

5. From Simple Cyclic 1,3-Ketoamides to Complex Spirolactams by Supported Heterogeneous Organocatalysis with PS-BEMP;Synthesis;2016-07-12

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