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Journal of Medicinal Chemistry|March 4, 1994

Synthesis of naltrexone-derived delta-opioid antagonists. Role of conformation of the delta address moietyP S Portoghese, M Sultana, S T Moe, et al.

Journal of Medicinal Chemistry|February 3, 1995

7'-Substituted amino acid conjugates of naltrindole. Hydrophilic groups as determinants of selective antagonism of delta 1 opioid receptor-mediated antinociception in miceP S Portoghese, F Farouz-Grant, M Sultana, et al.

Journal of Medicinal Chemistry|September 1, 1986

Synthesis and opioid antagonist potencies of naltrexamine bivalent ligands with conformationally restricted spacersP S Portoghese, G Ronsisvalle, D L Larson, et al.

Journal of Medicinal Chemistry|November 12, 1993

Possible contribution of a glutathione conjugate to the long-duration action of beta-funaltrexamineD L Larson, M Hua, A E Takemori, et al.

Science (New York, N.Y.)|April 20, 1979

Chloroxymorphamine, and opioid receptor site-directed alkylating agent having narcotic agonist activityT P Caruso, A E Takemori, D L Larson, et al.

Pharmacology, Biochemistry, and Behavior|April 1, 1982

Antagonism of morphine-induced behavioral suppression by opiate receptor alkylatorsR B Messing, P S Portoghese, A E Takemori, et al.

European Journal of Pharmacology|March 12, 1981

Antagonism by chlornaltrexamine of some effects of delta 9-tetrahydrocannabinol in ratsF C Tulunay, I H Ayhan, P S Portoghese, et al.

European Journal of Pharmacology|April 29, 1986

Effects of beta-funaltrexamine (beta-FNA) on morphine dependence in rats and monkeysM D Aceto, W L Dewey, P S Portoghese, et al.

European Journal of Pharmacology|October 8, 1985

beta-Funaltrexamine (beta-FNA) and neural tumor response in miceI S Zagon, P J McLaughlin, A E Takemori, et al.

Journal of Medicinal Chemistry|May 13, 1994

Structure-activity relationship of N17'-substituted norbinaltorphimine congeners. Role of the N17' basic group in the interaction with a putative address subsite on the kappa opioid receptorP S Portoghese, C E Lin, F Farouz-Grant, et al.

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Showing results (101-110 of 149) with videos related to

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Pageof 15

Journal of Medicinal Chemistry|March 4, 1994

Synthesis of naltrexone-derived delta-opioid antagonists. Role of conformation of the delta address moietyP S Portoghese, M Sultana, S T Moe, et al.

Journal of Medicinal Chemistry|February 3, 1995

7'-Substituted amino acid conjugates of naltrindole. Hydrophilic groups as determinants of selective antagonism of delta 1 opioid receptor-mediated antinociception in miceP S Portoghese, F Farouz-Grant, M Sultana, et al.

Journal of Medicinal Chemistry|September 1, 1986

Synthesis and opioid antagonist potencies of naltrexamine bivalent ligands with conformationally restricted spacersP S Portoghese, G Ronsisvalle, D L Larson, et al.

Journal of Medicinal Chemistry|November 12, 1993

Possible contribution of a glutathione conjugate to the long-duration action of beta-funaltrexamineD L Larson, M Hua, A E Takemori, et al.

Science (New York, N.Y.)|April 20, 1979

Chloroxymorphamine, and opioid receptor site-directed alkylating agent having narcotic agonist activityT P Caruso, A E Takemori, D L Larson, et al.

Pharmacology, Biochemistry, and Behavior|April 1, 1982

Antagonism of morphine-induced behavioral suppression by opiate receptor alkylatorsR B Messing, P S Portoghese, A E Takemori, et al.

European Journal of Pharmacology|March 12, 1981

Antagonism by chlornaltrexamine of some effects of delta 9-tetrahydrocannabinol in ratsF C Tulunay, I H Ayhan, P S Portoghese, et al.

European Journal of Pharmacology|April 29, 1986

Effects of beta-funaltrexamine (beta-FNA) on morphine dependence in rats and monkeysM D Aceto, W L Dewey, P S Portoghese, et al.

European Journal of Pharmacology|October 8, 1985

beta-Funaltrexamine (beta-FNA) and neural tumor response in miceI S Zagon, P J McLaughlin, A E Takemori, et al.

Journal of Medicinal Chemistry|May 13, 1994

Structure-activity relationship of N17'-substituted norbinaltorphimine congeners. Role of the N17' basic group in the interaction with a putative address subsite on the kappa opioid receptorP S Portoghese, C E Lin, F Farouz-Grant, et al.

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