New 2-heterocyclyl-imidazo[2,1-i]purin-5-one derivatives as potent and selective human A3 adenosine receptor antagonists. [electronic resource]
Producer: 20111010Description: 5205-20 p. digitalISSN:- 1520-4804
- Adenosine A3 Receptor Antagonists -- chemical synthesis
- Amino Acid Sequence
- Animals
- CHO Cells
- Cricetinae
- Cricetulus
- Cyclic AMP -- biosynthesis
- Humans
- Ligands
- Models, Molecular
- Molecular Sequence Data
- Purines -- chemical synthesis
- Radioligand Assay
- Receptor, Adenosine A2B -- genetics
- Receptor, Adenosine A3 -- chemistry
- Sequence Alignment
- Stereoisomerism
- Structure-Activity Relationship
- Transfection
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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