Design, synthesis, and evaluation of fused heterocyclic analogs of SCH 58261 as adenosine A2A receptor antagonists-Reference-Cited by-同舟云学术

Design, synthesis, and evaluation of fused heterocyclic analogs of SCH 58261 as adenosine A2A receptor antagonists

Published:2008-07 Issue:14 Volume:18 Page:4204-4209
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Shah Unmesh,Lankin Claire M.,Boyle Craig D.,Chackalamannil Samuel,Greenlee William J.,Neustadt Bernard R.,Cohen-Williams Mary E.,Higgins Guy A.,Ng Kwokei,Varty Geoffrey B.,Zhang Hongtao,Lachowicz Jean E.

Publisher

Elsevier BV

Subject

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

Reference29 articles.

1. Biaryl and heteroaryl derivatives of SCH 58261 as potent and selective adenosine A2A receptor antagonists

2. Stimulation of high-affinity adenosine A2 receptors decreases the affinity of dopamine D2 receptors in rat striatal membranes.

3. Schwarzschild, M. A., guest editor. Prog. Neurobiol. 2007, 83, 261. Special Issue: Targeting Adenosine A2A Receptors in Parkinson’s Disease and Other CNS Disorders.

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