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

  作者 Gillespie, RJ; Cliffe, IA; Dawson, CE; Dourish, CT; Gaur, S; Giles, PR; Jordan, AM; Knight, AR; Lawrence, A; Lerpiniere, J; Misra, A; Pratt, RM; Todd, RS; Upton, R; Weiss, SM; Williamson, DS  
  选自 期刊  Bioorganic & Medicinal Chemistry Letters;  卷期  2008年18-9;  页码  2920-2923  
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[摘要]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. (C) 2008 Elsevier Ltd. All rights reserved.

 
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