Opioid binding profiles of new hydrazone, oxime, carbazone and semicarbazone derivatives of 14-alkoxymorphinans

被引:51
作者
Monory, K
Greiner, E
Sartania, N
Sallai, L
Pouille, Y
Schmidhammer, H
Hanoune, J
Borsodi, A
机构
[1] Hungarian Acad Sci, Biol Res Ctr, Inst Biochem, H-6701 Szeged, Hungary
[2] INSERM, U99, Creteil, France
[3] Univ Innsbruck, Inst Pharmaceut Chem, A-6020 Innsbruck, Austria
基金
匈牙利科学研究基金会;
关键词
mu opioid receptor; affinity label; in vitro receptor binding; alkoxymorphinans;
D O I
10.1016/S0024-3205(99)00148-4
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Several hydrazone, oxime, carbazone and semicarbazone derivatives of 14-alkoxycodeinones and 14-alkoxydihydrocodeinones were synthesised [1] and characterised in in vitro radioligand binding assays in rat brain membrane preparations. The tested compounds show the highest affinity for the mu opioid binding sites and most of them have agonist character. Subtype analysis of the binding shows mu(2) specificity. However, some of these ligands are able to block partially (40-60%) the high affinity (putative mu(1)) opioid binding sites while all of them act as reversible ligands at the low affinity (putative mu(2)) sites.
引用
收藏
页码:2011 / 2020
页数:10
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