Antagonists of the human adenosine A2A receptor. Part 3: Design and synthesis of pyrazolo[3,4-d]pyrimidines, pyrrolo[2,3-d]pyrimidines and 6-arylpurines-Reference-Cited by-同舟云学术

Antagonists of the human adenosine A2A receptor. Part 3: Design and synthesis of pyrazolo[3,4-d]pyrimidines, pyrrolo[2,3-d]pyrimidines and 6-arylpurines

Published:2008-05 Issue:9 Volume:18 Page:2924-2929
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Gillespie Roger J.,Cliffe Ian A.,Dawson Claire E.,Dourish Colin T.,Gaur Suneel,Jordan Allan M.,Knight Antony R.,Lerpiniere Joanne,Misra Anil,Pratt Robert M.,Roffey Jonathan,Stratton Gemma C.,Upton Rebecca,Weiss Scott M.,Williamson Douglas S.

Publisher

Elsevier BV

Subject

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

Reference16 articles.

1. Therapeutic potential of adenosine A2A receptor antagonists in Parkinson's disease

2. Highlights on the Development of A2A Adenosine Receptor Agonists and Antagonists

3. Antagonists of the human adenosine A2A receptor. Part 2: Design and synthesis of 4-arylthieno[3,2-d]pyrimidine derivatives

4. Experimental Models of Parkinson's Disease: From the Static to the Dynamic

5. Adenosine A2 receptors modulate haloperidol-induced catalepsy in rats

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