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4-Amido-2-Aryl-1, 2, 4-Triazolo[4, 3-A]quinoxalin-1-Ones as New Potent and Selective Human A3 Adenosine Receptor Antagonists. Synthesis, Pharmacological Evaluation, and Ligand-Receptor Modeling Studies
doi 10.1021/jm060373w.s001
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American Chemical Society (ACS)
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