Selective δ opioid receptor agonists for inflammatory and neuropathic pain

被引:25
作者
Dondio, G [1 ]
Ronzoni, S [1 ]
Farina, C [1 ]
Graziani, D [1 ]
Parini, C [1 ]
Petrillo, P [1 ]
Giardina, GAM [1 ]
机构
[1] SmithKline Beecham SpA, I-20021 Milan, Italy
来源
FARMACO | 2001年 / 56卷 / 1-2期
关键词
delta opioid agonist; pyrrolomorphinan; message-address concept; pain;
D O I
10.1016/S0014-827X(01)01020-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the last decade a number of selective and potent non-peptidic agents became available to explore the usefulness of the delta-opioid receptor in modulation of pain of different origins. As a continuing effort in this field, potent and selective delta-opioid agonists based on the pyrrolomorphinan framework have been designed, synthesised and characterised biologically in our laboratories. In animal models, a selected compound of interest, SB 235863, has proved the concept that selective delta-opioid agonists may have great potential as pain relief agents in inflammatory and neuropathic pain conditions. Importantly, such a compound was free of the unwanted side effects usually associated with narcotic analgesics such as morphine. (C) 2001 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:117 / 119
页数:3
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