Paper
Opioid receptor binding and in vivo antinociceptive activity of position 3-substituted morphiceptin analogs.
Published Jul 23, 2004 · J. Fichna, Jean‐Claude Do‐Régo, J. Costentin
Biochemical and biophysical research communications
Q1 SJR score
34
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0
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Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
[D-1-Nal3]Morphiceptin is the most potent position 3-substituted morphiceptin analog, with a 26-fold increase in mu-opioid receptor affinity and significant in vivo analgesic activity compared to morphiceptin.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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