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Journal Abstract Search

112 related items for PubMed ID: 9424015

  • 1. Etorphines: mu-opioid receptor-selective antinociception and low physical dependence capacity.
    Aceto MD, Harris LS, Bowman ER.
    Eur J Pharmacol; 1997 Nov 12; 338(3):215-23. PubMed ID: 9424015
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  • 2. Antinociceptive effect of dihydroetorphine in diabetic mice.
    Kamei J, Suzuki T, Misawa M, Nagase H, Kasuya Y.
    Eur J Pharmacol; 1995 Feb 24; 275(1):109-13. PubMed ID: 7774657
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  • 3. Dihydroetorphine is a mu-receptor-selective ligand.
    Wang DX, Lu XQ, Qin BY.
    J Pharm Pharmacol; 1995 Aug 24; 47(8):669-73. PubMed ID: 8583370
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  • 4. Opioid agonist efficacy predicts the magnitude of tolerance and the regulation of mu-opioid receptors and dynamin-2.
    Pawar M, Kumar P, Sunkaraneni S, Sirohi S, Walker EA, Yoburn BC.
    Eur J Pharmacol; 2007 Jun 01; 563(1-3):92-101. PubMed ID: 17349996
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  • 5. Discriminative stimulus and antinociceptive effects of dihydroetorphine in rhesus monkeys.
    Gerak LR, Gauthier CR, France CR.
    Psychopharmacology (Berl); 2003 Apr 01; 166(4):351-9. PubMed ID: 12601499
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  • 6. Agonist and antagonist properties of dihydroetorphine for mu-opioid receptors in mice.
    Kamei J, Suzuki T, Nagase H.
    Neurosci Lett; 1996 Sep 06; 215(2):87-90. PubMed ID: 8888002
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  • 7. Binding affinity to and dependence on some opioids in Sf9 insect cells expressing human mu-opioid receptor.
    Liu ZH, He Y, Jin WQ, Chen XJ, Zhang HP, Shen QX, Chi ZQ.
    Acta Pharmacol Sin; 2003 Sep 06; 24(9):859-63. PubMed ID: 12956932
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  • 8. In vivo pharmacological characterization of SoRI 9409, a nonpeptidic opioid mu-agonist/delta-antagonist that produces limited antinociceptive tolerance and attenuates morphine physical dependence.
    Wells JL, Bartlett JL, Ananthan S, Bilsky EJ.
    J Pharmacol Exp Ther; 2001 May 06; 297(2):597-605. PubMed ID: 11303048
    [Abstract] [Full Text] [Related]

  • 9. Antinociceptive effect of dihydroetorphine and its tolerance/dependence liability in mice.
    Tokuyama S, Takahashi M, Kaneto H.
    Biol Pharm Bull; 1993 Aug 06; 16(8):774-7. PubMed ID: 8220323
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  • 17. Studies on the abstinence-like overshoot following reversal of the potent 19-isoamyl derivative of etorphine with naloxone. A comparison with the opioids fentanyl and alfentanil.
    Freye E, Neruda B, Smith OW.
    Arzneimittelforschung; 1997 Jan 06; 47(1):6-9. PubMed ID: 9037435
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  • 18. Involvement of supraspinal epsilon and mu opioid receptors in inhibition of the tail-flick response induced by etorphine in the mouse.
    Xu JY, Fujimoto JM, Tseng LF.
    J Pharmacol Exp Ther; 1992 Oct 06; 263(1):246-52. PubMed ID: 1328609
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  • 19. Involvement of mu-opioid receptors and alpha-adrenoceptors in the immunomodulatory effects of dihydroetorphine.
    Wu WR, Zheng JW, Li FY, Li Y, Zhang KR, Bai HQ.
    Eur J Pharmacol; 1998 Jul 17; 353(1):79-85. PubMed ID: 9721043
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  • 20. Ultra-low doses of naltrexone or etorphine increase morphine's antinociceptive potency and attenuate tolerance/dependence in mice.
    Shen KF, Crain SM.
    Brain Res; 1997 May 23; 757(2):176-90. PubMed ID: 9200746
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