Vincent Setola, Ph.D.

Case Western Reserve University, Cleveland Heights, OH, United States 
Psychopharmacology, 5-HT2A receptors, hallucinogens
"Vincent Setola"
Mean distance: 15.89 (cluster 6)


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Bryan L. Roth grad student 2005 Case Western
 (Discovering the molecular and cellular mechanisms underlying fenfluramine-induced cardiopulmonary side effects.)
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Roth BL, Gibbons S, Arunotayanun W, et al. (2018) Correction: The Ketamine Analogue Methoxetamine and 3- and 4-Methoxy Analogues of Phencyclidine Are High Affinity and Selective Ligands for the Glutamate NMDA Receptor. Plos One. 13: e0194984
Polepally PR, Huben K, Vardy E, et al. (2014) Michael acceptor approach to the design of new salvinorin A-based high affinity ligands for the kappa-opioid receptor. European Journal of Medicinal Chemistry. 85: 818-29
Sampson D, Bricker B, Zhu XY, et al. (2014) Further evaluation of the tropane analogs of haloperidol. Bioorganic & Medicinal Chemistry Letters. 24: 4294-7
Sampson D, Zhu XY, Eyunni SV, et al. (2014) Identification of a new selective dopamine D4 receptor ligand. Bioorganic & Medicinal Chemistry. 22: 3105-14
Kimple AJ, Garland AL, Cohen SP, et al. (2014) RGS21, a regulator of taste and mucociliary clearance? The Laryngoscope. 124: E56-63
Arunotayanun W, Dalley JW, Huang XP, et al. (2013) An analysis of the synthetic tryptamines AMT and 5-MeO-DALT: emerging 'Novel Psychoactive Drugs'. Bioorganic & Medicinal Chemistry Letters. 23: 3411-5
Roth BL, Gibbons S, Arunotayanun W, et al. (2013) The ketamine analogue methoxetamine and 3- and 4-methoxy analogues of phencyclidine are high affinity and selective ligands for the glutamate NMDA receptor. Plos One. 8: e59334
Kokel D, Cheung CY, Mills R, et al. (2013) Photochemical activation of TRPA1 channels in neurons and animals. Nature Chemical Biology. 9: 257-63
Iversen L, Gibbons S, Treble R, et al. (2013) Neurochemical profiles of some novel psychoactive substances. European Journal of Pharmacology. 700: 147-51
Wu H, Li J, Fronczek FR, et al. (2013) Labdane diterpenoids from Leonotis leonurus. Phytochemistry. 91: 229-35
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