共 64 条
The opioid-receptor-like 1 (ORL-1) as a potential target for new analgesics
被引:20
作者:

Barlocco, D
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h-index: 0
机构: Univ Milan, Ist Chim Farmaceut & Tossicol, I-20131 Milan, Italy

Cignarella, G
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h-index: 0
机构: Univ Milan, Ist Chim Farmaceut & Tossicol, I-20131 Milan, Italy

Giardina, GAM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Milan, Ist Chim Farmaceut & Tossicol, I-20131 Milan, Italy

Toma, L
论文数: 0 引用数: 0
h-index: 0
机构: Univ Milan, Ist Chim Farmaceut & Tossicol, I-20131 Milan, Italy
机构:
[1] Univ Milan, Ist Chim Farmaceut & Tossicol, I-20131 Milan, Italy
[2] SmithKline Beecham SpA, Dept Med Chem, I-20021 Milan, Italy
[3] Univ Pavia, Dipartimento Chim Organ, I-27100 Pavia, Italy
关键词:
analgesia;
opioid-receptor-like 1 (ORL-1);
nociceptin;
orphanin FQ;
D O I:
10.1016/S0223-5234(00)00126-4
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
A new sequence, which encoded a novel G protein-coupled receptor, was disclosed by two different groups, using the nucleic acid probes based on the delta opioid receptor, first cloned in 1992. The new receptor, which Meunier called opioid-receptor-like 1 (ORL-1), was shown to share high homology with the opioid receptors and therefore thought to be a potential target for new analgesics. In this respect, the present review reports on the literature referring to ORL-1, to its natural ligand (nociceptin or orphanin FQ) and to several synthetic analogues recently described, both as agonists or antagonists at the receptor. (C) 2000 Editions scientifiques er medicales Elsevier SAS.
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页码:275 / 282
页数:8
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