N6-Substituted adenosine derivatives: selectivity, efficacy, and species differences at A3 adenosine receptors.
第一作者:
Zhan-Guo,Gao
第一单位:
Molecular Recognition Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Room B1A-19, Building 8A, Bethesda, MD 20892, USA.
作者:
医学主题词
腺苷(Adenosine);动物(Animals);结合, 竞争性(Binding, Competitive);CHO细胞(CHO Cells);仓鼠亚科(Cricetinae);环AMP(Cyclic AMP);人类(Humans);大鼠(Rats);受体, 腺苷A3(Receptor, Adenosine A3);受体, 嘌呤能P1(Receptors, Purinergic P1);种特异性(Species Specificity);构效关系(Structure-Activity Relationship)
DOI
10.1016/s0006-2952(03)00153-9
PMID
12754103
发布时间
2025-05-29
- 浏览22
Biochemical pharmacology
1675-84页
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