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clocinnamox
Known as:
14-beta-(4-chlorocinnamoylamino)-7,8-dihydro-N-cyclopropylmethylnorpmorphine mesylate
National Institutes of Health
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Related topics
Related topics
4 relations
Broader (3)
Cinnamates
Morphine Derivatives Including Cocaine
Narcotic Antagonists
methoclocinnamox
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Tingenone, a Pentacyclic Triterpene, Induces Peripheral Antinociception Due to Opioidergic Activation
C. Veloso
,
V. Rodrigues
,
+5 authors
A. Perez
Planta Medica
2014
Corpus ID: 8237884
Abstract Plants belonging to the genus Maytenus are routinely used in folk medicine for the treatment of pain diseases. Our…
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2009
2009
Experimental Utility and Clinical Potential of Irreversible Opioid Antagonists
E. Walker
,
S. Comer
,
S. Comer
2009
Corpus ID: 68035337
In opioid pharmacology, irreversible, insurmountable antagonists have been critical experimental tools to characterize μ-opioid…
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2002
2002
CLOCINNAMOX BLOCKS ONLY MU RECEPTORS IRREVERSIBLY : BINDING
Evidence Zernig
,
Burke
,
Jw Lewis
,
J. Woods
2002
Corpus ID: 32972596
In rhesus monkey antinociception experiments, the cinnamoylaminomorphinone opioid antagonist cloeinnamox at a dose of 0.1 mg/kg…
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2000
2000
3-Deoxyclocinnamox: the first high-affinity, nonpeptide mu-opioid antagonist lacking a phenolic hydroxyl group.
I. Derrick
,
C. Neilan
,
+4 authors
J. Lewis
Journal of Medicinal Chemistry
2000
Corpus ID: 23255292
The C(3)-substituent in morphinan opioids is of critical importance; the 3-OH group is usually associated with very much higher…
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1998
1998
Oral ethanol-reinforced responding in rhesus monkeys: effects of opioid antagonists selective for the mu-, kappa-, or delta-receptor.
K. Williams
,
J. Woods
Alcoholism: Clinical and Experimental Research
1998
Corpus ID: 25428621
To determine the mechanism by which naltrexone (NTX) reduces oral ethanol-reinforced responding, opioid antagonists that show mu…
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1998
1998
The role of endogenous opioids in the luteinizing hormone surge in rats: studies with clocinnamox, a long-lasting opioid receptor antagonist.
P. Lieberman
,
J. Woods
,
E. Young
European Journal of Pharmacology
1998
Corpus ID: 25786654
1997
1997
Clocinnamox dose-dependently antagonizes morphine-analgesia and [3H]DAMGO binding in rats.
C. Paronis
,
J. Woods
European Journal of Pharmacology
1997
Corpus ID: 22257138
1996
1996
Clocinnamox antagonism of opioid suppression of schedule-controlled responding in rhesus monkeys
E. Butelman
,
S. Negus
,
J. Woods
,
J. Lewis
Psychopharmacology
1996
Corpus ID: 17282330
The antagonist effects of clocinnamox were evaluated against opioid agonists, acting at μ, κ and ∂-receptors, in rhesus monkeys…
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1996
1996
In vivo apparent pA2 analysis in rats treated with either clocinnamox or morphine
E. Walker
,
T. M. Richardson
,
A. Young
Psychopharmacology
1996
Corpus ID: 10826724
Experiments tested the hypothesis that loss of agonist potency or effectiveness following irreversible antagonist or chronic…
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1995
1995
The effect of the irreversible mu-opioid receptor antagonist clocinnamox on morphine potency, receptor binding and receptor mRNA.
K. Chan
,
M. Brodsky
,
T. Davis
,
S. Franklin
,
C. Inturrisi
,
B. Yoburn
European Journal of Pharmacology
1995
Corpus ID: 23810093
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