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The following term was not found in PubMed: 4406-22-8
Page 1
Delta opioid antagonist, 16-Me cyprenorphine, selectively attenuates conditional fear- and DPDPE-induced analgesia on the formalin test.
Fanselow MS, Calcagnetti DJ, Helmstetter FJ. Fanselow MS, et al. Pharmacol Biochem Behav. 1989 Feb;32(2):469-73. doi: 10.1016/0091-3057(89)90181-0. Pharmacol Biochem Behav. 1989. PMID: 2542994 Free article.
The effects of 16-Me cyprenorphine (M80) on the antinociception produced by reexposing rats to a chamber associated with footshock (1 mA, 0.75 sec) 24 hr earlier was assessed with the formalin test. ...
The effects of 16-Me cyprenorphine (M80) on the antinociception produced by reexposing rats to a chamber associated with footshock (1 …
Centrally administered opioid antagonists, nor-binaltorphimine, 16-methyl cyprenorphine and MR2266, suppress intake of a sweet solution.
Calcagnetti DJ, Calcagnetti RL, Fanselow MS. Calcagnetti DJ, et al. Pharmacol Biochem Behav. 1990 Jan;35(1):69-73. doi: 10.1016/0091-3057(90)90206-w. Pharmacol Biochem Behav. 1990. PMID: 2315372
Three opioid antagonists (MR2266, 16-methyl cyprenorphine and nor-binaltorphimine) were tested independently for their ability to suppress the intake of a highly palatable saccharin and glucose (S/G) solution after central administration. MR2266 is an equally potent antago …
Three opioid antagonists (MR2266, 16-methyl cyprenorphine and nor-binaltorphimine) were tested independently for their ability to sup …
Swim-stress-induced antinociception in young rats.
Jackson HC, Kitchen I. Jackson HC, et al. Br J Pharmacol. 1989 Mar;96(3):617-22. doi: 10.1111/j.1476-5381.1989.tb11860.x. Br J Pharmacol. 1989. PMID: 2720296 Free PMC article.
A 3 min swim in 20 and 25 day old rats produced marked antinociception which was blocked by naloxone, Mr 1452, 16-methyl cyprenorphine and levallorphan but not Mr 1453 or N-methyl levallorphan. ...
A 3 min swim in 20 and 25 day old rats produced marked antinociception which was blocked by naloxone, Mr 1452, 16-methyl cyprenorphine …
Subcellular distribution of etorphine in rat brain and evidence for in vitro stereospecific binding.
Cerletti C, Coccia P, Manara L, Mennini T, Recchia M. Cerletti C, et al. Br J Pharmacol. 1978 Jan;62(1):31-8. doi: 10.1111/j.1476-5381.1978.tb07003.x. Br J Pharmacol. 1978. PMID: 620097 Free PMC article.
Different distribution profiles in the subcellular fractions were observed at these two dose levels. 3 Concurrent administration of either cyprenorphine or naloxone with intravenous etorphine, caused a shift of the labelled drug from the P3 fraction to the supernatant frac …
Different distribution profiles in the subcellular fractions were observed at these two dose levels. 3 Concurrent administration of either …
16-Me cyprenorphine (RX 8008M): a potent opioid antagonist with some delta selectivity.
Smith CF. Smith CF. Life Sci. 1987 Jan 19;40(3):267-74. doi: 10.1016/0024-3205(87)90342-0. Life Sci. 1987. PMID: 3025546
16-Me cyprenorphine (RX 8008M) has been investigated in a number of isolated tissue preparations and found to be a pure opioid antagonist with Ke values at the delta, mu and kappa receptors of 0.73, 1.77 and 59.6 nM respectively. ...
16-Me cyprenorphine (RX 8008M) has been investigated in a number of isolated tissue preparations and found to be a pure opioid antago …
Differential effects of selective opioid peptide antagonists on the acquisition of pavlovian fear conditioning.
Fanselow MS, Kim JJ, Young SL, Calcagnetti DJ, DeCola JP, Helmstetter FJ, Landeira-Fernandez J. Fanselow MS, et al. Peptides. 1991 Sep-Oct;12(5):1033-7. doi: 10.1016/0196-9781(91)90056-u. Peptides. 1991. PMID: 1686930
On the other hand, the kappa antagonist nor-binaltorphimine reduced conditioning. Two delta antagonist treatments (16-methyl cyprenorphine and naltrindole) had no reliable effect on acquisition. ...
On the other hand, the kappa antagonist nor-binaltorphimine reduced conditioning. Two delta antagonist treatments (16-methyl cyprenorphin …
[D-Ala2,Leu5,Cys6]enkephalin: short-term agonist effects and long-term antagonism at delta opioid receptors.
Calcagnetti DJ, Fanselow MS, Helmstetter FJ, Bowen WD. Calcagnetti DJ, et al. Peptides. 1989 Mar-Apr;10(2):319-26. doi: 10.1016/0196-9781(89)90037-5. Peptides. 1989. PMID: 2547203 Free article.
In the second experiment, we determined that immobility was attenuated by pretreatment with naltrexone methobromide (QNTX, 0.1 microgram), and the delta selective antagonist, 16-methyl cyprenorphine (M80, 5 micrograms). QNTX and M80 significantly attenuated DALCE-induced i …
In the second experiment, we determined that immobility was attenuated by pretreatment with naltrexone methobromide (QNTX, 0.1 microgram), a …
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