The novel compound (±)-1-[10-((E)-3-Phenyl-allyl)-3,10-diaza-bicyclo[4.3.1]dec-3-yl]-propan-1-one (NS7051) attenuates nociceptive transmission in animal models of experimental pain; a pharmacological comparison with the combined μ-opioid receptor agonist and monoamine reuptake inhibitor tramadol-Reference-Cited by-同舟云学术

The novel compound (±)-1-[10-((E)-3-Phenyl-allyl)-3,10-diaza-bicyclo[4.3.1]dec-3-yl]-propan-1-one (NS7051) attenuates nociceptive transmission in animal models of experimental pain; a pharmacological comparison with the combined μ-opioid receptor agonist and monoamine reuptake inhibitor tramadol

Published:2008-02 Issue:2 Volume:54 Page:331-343
ISSN:0028-3908
Container-title:Neuropharmacology
language:en
Short-container-title:Neuropharmacology

Author:

Munro Gordon,Bæk Camilla Æ.,Erichsen Helle K.,Nielsen Alexander N.,Nielsen Elsebet Ø.,Scheel-Kruger Jørgen,Weikop Pia,Peters Dan

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Pharmacology

Reference44 articles.

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