European Journal of Medicinal Chemistry p. 133 - 139 (1995)
Update date:2022-08-03
Topics:
Colotta, V.
Cecchi, L.
Catarzi, D.
Filacchioni, G.
Martini, C.
et al.
The syntheses, A%1 and A2a adenosine receptor affinities and structure-activity relationships of some 2-aryl-1,2,4-triazolo<1,5-a>quinoxalines, 2-arylimidazo<1,2-a>quinoxalines, 1-arylimidazo<1,5-a>quinoxalines are reported and compared with that of a previously reported 2-phenylpyrazolo<1,5-a>quinoxaline.The results show that some triazoloquinoxalines are potent and specific A1 adenosine receptor ligands and that the replacement of either nitrogen at position 1 or 3 of the triazoloquinoxaline moiety with a CH brought about a decrease in affinity at both adenosine receptors. adenosine receptor ligand / 1,2,4-triazolo<1,5-a>quinoxaline / imidazo<1,2-a>quinoxaline / imidazo<1,5-a>quinoxaline / tricyclic heteroaromatic system
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