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Brain Research Bulletin|September 12, 2007
DAMGO and 6beta-glycine substituted 14-O-methyloxymorphone but not morphine show peripheral, preemptive antinociception after systemic administration in a mouse visceral pain model and high intrinsic efficacy in the isolated rat vas deferensMahmoud Al-Khrasani, Mariana Spetea, Tamas Friedmann, et al.Journal of Medicinal Chemistry|April 29, 2005
Synthesis and biological evaluation of 14-alkoxymorphinans. 22.(1) Influence of the 14-alkoxy group and the substitution in position 5 in 14-alkoxymorphinan-6-ones on in vitro and in vivo activitiesRoberta Lattanzi, Mariana Spetea, Falko Schüllner, et al.Current Pharmaceutical Design|March 2, 2013
Functionalization of the carbonyl group in position 6 of morphinan-6-ones. Development of novel 6-amino and 6-guanidino substituted 14-alkoxymorphinansHelmut Schmidhammer, Mariana Spetea, Petra Windisch, et al.Journal of Medicinal Chemistry|August 22, 2017
Highly Potent and Selective New Diphenethylamines Interacting with the κ-Opioid Receptor: Synthesis, Pharmacology, and Structure-Activity RelationshipsFilippo Erli, Elena Guerrieri, Tanila Ben Haddou, et al.Journal of Medicinal Chemistry|September 5, 2003
Synthesis and biological evaluation of 14-alkoxymorphinans. 20. 14-phenylpropoxymetopon: an extremely powerful analgesicJohannes Schütz, Mariana Spetea, Martin Koch, et al.The European Journal of Neuroscience|July 31, 2003
Binding characteristics of [3H]14-methoxymetopon, a high affinity mu-opioid receptor agonistMariana Spetea, Fanni Tóth, Johannes Schütz, et al.Journal of Medicinal Chemistry|October 21, 2017
Synthesis, Pharmacology, and Molecular Docking Studies on 6-Desoxo-N-methylmorphinans as Potent μ-Opioid Receptor AgonistsMaria Dumitrascuta, Tanila Ben Haddou, Elena Guerrieri, et al.European Journal of Pharmacology|January 20, 2004
In vitro opioid activity profiles of 6-amino acid substituted derivatives of 14-O-methyloxymorphoneMariana Spetea, Tamas Friedmann, Pal Riba, et al.European Journal of Pharmacology|January 14, 2003
14-Methoxymetopon, a very potent mu-opioid receptor-selective analgesic with an unusual pharmacological profileMichael A King, Wendy Su, Claire L Nielan, et al.British Journal of Pharmacology|May 12, 2017
Selective κ receptor partial agonist HS666 produces potent antinociception without inducing aversion after i.c.v. administration in miceMariana Spetea, Shainnel O Eans, Michelle L Ganno, et al.Pageof 6