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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
2018
Review
2018
Classical opioid analgesics, including morphine, mediate all of their desired and undesired effects by specific activation of the… Expand
Review
2004
Review
2004
The thevinols and orvinols derived from thebaine via the thebaine-methylvinyl ketone adduct (thevinone) were thoroughly… Expand
2002
2002
In screening cytotoxic agents in morphine alkaloids [TE1-10], codeinone [TE8] was cytotoxic against two human oral tumor cells… Expand
2000
2000
Iatrogenic tolerance and physical dependence have been documented in human neonates and infants infused with fentanyl or morphine… Expand
1999
1999
This study examines the possibility that oripavine opioid receptor agonists bind equally to both high and low affinity states of… Expand
Highly Cited
1997
Highly Cited
1997
Mu opioid receptors are subject to phosphorylation and desensitization through actions of at least two distinct biochemical… Expand
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
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
1993
1993
The profile of actions of dihydroetorphine (DHE) concerning antinociception, tolerance and dependence was compared with those of… Expand
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