| Literature DB >> 11347951 |
G Dondio1, S Ronzoni, C Farina, D Graziani, C Parini, P Petrillo, G A Giardina.
Abstract
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.Entities:
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Year: 2001 PMID: 11347951 DOI: 10.1016/s0014-827x(01)01020-5
Source DB: PubMed Journal: Farmaco ISSN: 0014-827X