期刊
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 23, 期 9, 页码 2688-2691出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2013.02.078
关键词
Adenosine; A(2A) antagonists; Parkinson's disease; Catalepsy
A novel series of benzyl substituted thieno[2,3-d]pyrimidines were identified as potent A(2A) receptor antagonists. Several five- and six-membered heterocyclic replacements for the optimized methylfuran were explored. Select compounds effectively reverse catalepsy in mice when dosed orally. (C) 2013 Elsevier Ltd. All rights reserved.
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