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By G. Hasko
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12. O. , 2-Substitution of N6-benzyladenosine-5′-uronamides enhances selectivity for A3 adenosine receptors, J. Med. , 37, 3614, 1994. 13. E. , 125I-4-aminobenzyl-5′-N-methylcarboxamidoadenosine, a high affinity radioligand for the rat A3 adenosine receptor, Mol. , 45, 978, 1994. 14. G. , Structural determinants of A3 adenosine receptor activation: nucleoside ligands at the agonist/antagonist boundary, J. Med. , 45, 4471, 2002. 15. G. , Novel N6-(substituted-phenylcarbamoyl)adenosine-5′-uronamides as potent agonists for A3 adenosine receptors, J.
A binding site model and structure-activity relationships for the rat A3 adenosine receptor, Mol. , 45, 1101, 1994. 35. , Cloned adenosine A3 receptors: pharmacological properties, species differences and receptor functions, Trends Pharmacol. , 15, 298, 1994. 36. L. , 6-phenyl-1,4-dihydropyridine derivatives as potent and selective A3 adenosine receptor antagonists, J. Med. , 39, 4667, 1996. 37. Jiang, J. , Structure-activity relationships of 4-(phenylethynyl)-6-phenyl-1,4dihydropyridines as highly selective A3 adenosine receptor antagonists, J.
50. G. , New 2-arylpyrazolo[4,3-c]quinoline derivatives as potent and selective human A3 adenosine receptor antagonists, J. Med. , 48, 5001, 2005. 51. E. , Isoquinoline and quinazoline urea analogues as antagonists for the human adenosine A3 receptor, J. Med. , 43, 2227, 2000. 52. G. , Allosteric modulation of A3 adenosine receptors by a series of 3-(2pyridinyl)isoquinoline derivatives, Mol. , 60, 1057, 2001. 53. E. , Thiazole and thiadiazole analogues as a novel class of adenosine receptor antagonists, J.
Adenosine Receptors - Therapeutic Asps. for Inflamm., Immune Diseases by G. Hasko