Major effect of pyrrolic N-benzylation in norbinaltorphimine, the selective κ-opioid receptor antagonist

被引:5
作者
Chauvignac, C
Miller, CN
Srivastava, SK
Lewis, JW
Husbands, SM [1 ]
Traynon, JR
机构
[1] Univ Bath, Dept Pharm & Pharmacol, Bath BA2 7AY, Avon, England
[2] Univ Michigan, Dept Pharmacol, Ann Arbor, MI 48109 USA
关键词
D O I
10.1021/jm049172n
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Indolic N-benzylation of naltrindole reportedly extends the duration of delta-opioid receptor (DOR) antagonism. Similar modification of the kappa-opioid receptor (KOR) antagonist norBNI (1a) and its 17,17'-diNMe analogue (1d), a low potency mu-opioid receptor (MOR) partial agonist, was found to affect predominantly their MOR activity. When administered systemically in mouse antinociceptive assays, N-benzyl-norBNI (1b) had only MOR agonist activity of relatively short duration whereas on central administration it had only a KOR-antagonist action of extremely long duration.
引用
收藏
页码:1676 / 1679
页数:4
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