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18,19-dihydroetorphine

Known as: Dihydroetorphine 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2004
Review
2004
The thevinols and orvinols derived from thebaine via the thebaine-methylvinyl ketone adduct (thevinone) were thoroughly… Expand
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2002
2002
In screening cytotoxic agents in morphine alkaloids [TE1-10], codeinone [TE8] was cytotoxic against two human oral tumor cells… Expand
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1999
1999
This study examines the possibility that oripavine opioid receptor agonists bind equally to both high and low affinity states of… Expand
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1998
1998
Neuropathic pain has been suggested to be resistant to treatment with opiates. Such perceived lack of opioid responsiveness may… Expand
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Highly Cited
1997
Highly Cited
1997
Mu opioid receptors are subject to phosphorylation and desensitization through actions of at least two distinct biochemical… Expand
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Highly Cited
1997
Highly Cited
1997
Comparative analgesic studies revealed that dihydroetorphine was more potent than etorphine in the tail-flick and hot-plate tests… Expand
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1995
1995
We recently showed that the opioid alkaloids, etorphine, dihydroetorphine and diprenorphine, have remarkably potent antagonist… Expand
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Highly Cited
1994
Highly Cited
1994
At low (< nM) concentrations, mu, delta or kappa opioid peptides as well as morphine and other opioid alkaloids elicit dose… Expand
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1993
1993
The profile of actions of dihydroetorphine (DHE) concerning antinociception, tolerance and dependence was compared with those of… Expand
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1982
1982
  • M. Huang, B. Qin
  • Zhongguo yao li xue bao = Acta pharmacologica…
  • 1982
  • Corpus ID: 31694504
The analgesic, respiratory depressive, immobilizing effects and a cute toxicity of dihydroetorphine (DHE) have been evaluated and… Expand
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