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18,19-dihydroetorphine

Known as: Dihydroetorphine 
 
National Institutes of Health

Papers overview

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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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2001
2001
To evaluate the pharmacokinetic and pharmacodynamic characteristics of a novel opioid analgesic, dihydroetorphine (DHE… Expand
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2000
2000
Iatrogenic tolerance and physical dependence have been documented in human neonates and infants infused with fentanyl or morphine… 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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1997
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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1997
1997
These experiments examined whether dihydroetorphine (DHE) could serve as a reinforcer in rhesus monkeys and evoke the… Expand
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1994
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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