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Antagonists of the human adenosine A2A receptor. Part 2: Design and synthesis of 4-arylthieno[3,2-d]pyrimidine derivatives.
- Source :
-
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2008 May 01; Vol. 18 (9), pp. 2920-3. Date of Electronic Publication: 2008 Mar 30. - Publication Year :
- 2008
-
Abstract
- We describe herein the discovery and development of a series of 4-arylthieno[3,2-d]pyrimidines which are potent adenosine A(2A) receptor antagonists. These novel compounds show high degrees of selectivity against the human A(1), A(2B) and A(3) receptor sub-types. Moreover, a number of these compounds show promising activity in vivo, suggesting potential utility in the treatment of Parkinson's disease.
- Subjects :
- Adenosine A1 Receptor Antagonists
Adenosine A3 Receptor Antagonists
Antiparkinson Agents chemical synthesis
Humans
Models, Chemical
Pyrimidines chemical synthesis
Stereoisomerism
Structure-Activity Relationship
Adenosine A2 Receptor Antagonists
Antiparkinson Agents therapeutic use
Drug Design
Parkinsonian Disorders drug therapy
Pyrimidines therapeutic use
Subjects
Details
- Language :
- English
- ISSN :
- 1464-3405
- Volume :
- 18
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry letters
- Publication Type :
- Academic Journal
- Accession number :
- 18407496
- Full Text :
- https://doi.org/10.1016/j.bmcl.2008.03.076