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Life Sciences|January 1, 1994
Supraspinal delta receptor subtype activity of heroin and 6-monoacetylmorphine in Swiss Webster miceJ J Rady, A E Takemori, P S Portoghese, et al.The Journal of Pharmacology and Experimental Therapeutics|June 1, 1980
Pharmacological studies with an alkylating narcotic agonist, chloroxymorphamine, and antagonist, chlornaltrexamineT P Caruso, D L Larson, P S Portoghese, et al.Journal of Medicinal Chemistry|October 1, 1984
Design and synthesis of naltrexone-derived affinity labels with nonequilibrium opioid agonist and antagonist activities. Evidence for the existence of different mu receptor subtypes in different tissuesL M Sayre, D L Larson, A E Takemori, et al.Journal of Medicinal Chemistry|August 1, 1986
Activity of N-methyl-alpha- and -beta-funaltrexamine at opioid receptorsM S Mohamed, D L Larson, A E Takemori, et al.Journal of Medicinal Chemistry|August 1, 1977
Stereochemical studies on medicinal agents. 23. Synthesis and biological evaluation of 6-amino derivatives of naloxone and naltrexoneJ B Jiang, R N Hanson, P S Portoghese, et al.European Journal of Pharmacology|September 21, 1990
Long-acting agonist and antagonist activities of naltrexamine bivalent ligands in miceA E Takemori, C B Yim, D L Larson, et al.The Journal of Pharmacology and Experimental Therapeutics|July 1, 1988
Nor-binaltorphimine, a highly selective kappa-opioid antagonist in analgesic and receptor binding assaysA E Takemori, B Y Ho, J S Naeseth, et al.Journal of Medicinal Chemistry|October 30, 1992
Delta opioid antagonist activity and binding studies of regioisomeric isothiocyanate derivatives of naltrindole: evidence for delta receptor subtypesP S Portoghese, M Sultana, W L Nelson, et al.Journal of Medicinal Chemistry|May 23, 1997
7-Spiroindanyl derivatives of naltrexone and oxymorphone as selective ligands for delta opioid receptorsS Ohkawa, B DiGiacomo, D L Larson, et al.The Journal of Pharmacology and Experimental Therapeutics|August 1, 1995
Cold water swim stress- and delta-2 opioid-induced analgesia are modulated by spinal gamma-aminobutyric acidA receptorsP Killian, B B Holmes, A E Takemori, et al.Pageof 15