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Biochemical Pharmacology|March 22, 2016
Carbachol dimers as homobivalent modulators of muscarinic receptorsRosanna Matucci, Marta Nesi, Maria Vittoria Martino, et al.Journal of Medicinal Chemistry|June 12, 2008
Synthesis and pharmacological characterization of chiral pyrrolidinylfuran derivatives: the discovery of new functionally selective muscarinic agonistsSerena Scapecchi, Marta Nesi, Rosanna Matucci, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|April 8, 2020
6,7-Dimethoxy-2-phenethyl-1,2,3,4-tetrahydroisoquinoline amides and corresponding ester isosteres as multidrug resistance reversersLaura Braconi, Gianluca Bartolucci, Marialessandra Contino, et al.Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|February 12, 2025
Ibogalogs decrease neuropathic pain in mice through a mechanism involving crosstalk between 5-HT2A and mGlu2 receptorsHugo R Arias, Laura Micheli, Anders A Jensen, et al.European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|July 8, 2021
Type I and type II positive allosteric modulators of α7 nicotinic acetylcholine receptors induce antidepressant-like activity in mice by a mechanism involving receptor potentiation but not neurotransmitter reuptake inhibition. Correlation with mTOR intracellular pathway activationKatarzyna M Targowska-Duda, Barbara Budzynska, Agnieszka Michalak, et al.Journal of Medicinal Chemistry|February 20, 2007
Synthesis, affinity profile, and functional activity of muscarinic antagonists with a 1-methyl-2-(2,2-alkylaryl-1,3-oxathiolan-5-yl)pyrrolidine structureSilvia Dei, Cristina Bellucci, Michela Buccioni, et al.Neurochemistry International|June 5, 2024
Novel psychoplastogen DM506 reduces cue-induced heroin-seeking and inhibits tonic GABA currents in the Prelimbic CortexKassandra Looschen, Shailesh Narayan Khatri, Malabika Maulik, et al.Journal of Medicinal Chemistry|March 17, 2006
Highly chiral muscarinic ligands: the discovery of (2S,2'R,3'S,5'R)-1-methyl-2-(2-methyl-1,3-oxathiolan-5-yl)pyrrolidine 3-sulfoxide methyl iodide, a potent, functionally selective, M2 partial agonistSerena Scapecchi, Rosanna Matucci, Cristina Bellucci, et al.Molecules (Basel, Switzerland)|July 27, 2024
Dual Inhibitors of P-gp and Carbonic Anhydrase XII (hCA XII) against Tumor Multidrug Resistance with Piperazine ScaffoldLaura Braconi, Chiara Riganti, Astrid Parenti, et al.Journal of Medicinal Chemistry|September 14, 2007
Design, synthesis, and preliminary pharmacological evaluation of new quinoline derivatives as nicotinic ligandsLuca Guandalini, Monica Norcini, Katia Varani, et al.Pageof 8