Structure-activity relationship of N6-substituted D-4′-thioadenosine derivatives as potent and selective agonists at the human A3 adenosine receptor.

被引:0
|
作者
Jeong, LS
Shin, DH
Kim, HO
Jung, JY
Kim, HJ
Kim, WK
Melman, N
Gao, ZG
Jacobson, KA
机构
[1] Ewha Womans Univ, Coll Pharm, Med Chem Lab, Seoul, South Korea
[2] NIDDK, Mol Recognit Sect, NIH, Bethesda, MD 20892 USA
来源
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 2004年 / 227卷
关键词
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
258-MEDI
引用
收藏
页码:U54 / U54
页数:1
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