1,2,3-triazolo[1,5-a]quinoxalines: synthesis and binding to benzodiazepine and adenosine receptors

被引:51
|
作者
Bertelli, L
Biagi, G
Giorgi, I
Manera, C
Livi, O
Scartoni, V
Betti, L
Giannaccini, G
Trincavelli, L
Barili, PL
机构
[1] Univ Pisa, Dipartimento Sci Farmaceut, I-56126 Pisa, Italy
[2] Univ Pisa, Ist Policattedra Discipline Biol, I-56126 Pisa, Italy
[3] Univ Pisa, Dipartimento Bioorgan, I-56126 Pisa, Italy
关键词
1,2,3-triazolo[1,5-a]quinoxalines; benzodiazepine receptor binding; adenosine receptor binding;
D O I
10.1016/S0223-5234(98)80036-6
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This paper reports the synthesis and binding assays toward benzodiazepine and adenosine A(1) and A(2A) receptors of new 1,2,3-triazolo[1,5-a]quinoxalin-4-one derivatives. The prepared compounds show good affinity toward the benzodiazepine receptor (K-i 53-314 nM); the GABA ratio values suggest an inverse agonist activity for the N(5) unsubstituted compounds 6b-d and an agonist activity for the N(5) methylated compounds 7a-c. Some derivatives of both series show good affinity (Ki < 100 nM) and selectivity toward the adenosine A(1) receptorial subtype. (C) Elsevier, Paris.
引用
收藏
页码:113 / 122
页数:10
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