naloxazone

Known as: Morphinan-6-one, 4,5-epoxy-3,14-dihydroxy-17-(2-propenyl)-, hydrazone, (5alpha)-, naloxone-6-hydrazone 
 

Topic mentions per year

Topic mentions per year

1980-2004
051019802004

Papers overview

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2004
2004
1. Naloxazone, a hydrazone derivative of naloxone which blocks mouse brain opiate receptorsin vivo for over 24 hr, produced a… (More)
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1986
1986
Naloxonazine is a relatively selective mu 1 affinity label in binding studies. Like naloxazone, naloxonazine has proven valuable… (More)
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1984
1984
When rats are presented with a novel saccharin solution and immediately injected with either morphine or ethanol, they… (More)
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1983
1983
Cardiovascular effects of the high affinity, irreversible opiate antagonist, naloxazone, were investigated in conscious rats… (More)
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1983
1983
Behavioral and cardiorespiratory responses to a lethal dose of morphine were evaluated in rats pretreated with saline or… (More)
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1983
1983
The selective in vivo blockade of high affinity (mu1) opioid binding sites in mice by naloxazone reduced the analgesic potency of… (More)
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1982
1982
The analgesic responses following morphine and cold-water swims (CWS) can be dissociated from each other. Indeed, certain… (More)
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Highly Cited
1981
Highly Cited
1981
Detailed competitive displacement curves of 3H-labeled [D-Ala2,Met5]enkephalinamide, [D-Ala2,D-Leu5]enkephalin, and… (More)
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1980
1980
Administration of naloxazone, a hydrazone derivative of naloxone, to intact mice produces a prolonged inhibition of in vitro [3H… (More)
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1980
1980
The receptor binding of the kappa agonist [3H]ethylketocyclazocine to brain homogenates in vitro and ketocyclazocine (kappa… (More)
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