An opioid agonist that does not induce mu-opioid receptor--arrestin interactions or receptor internalization von Groer, C E, Tidgewell, K, Moyer, R A, Harding, W W, Rothman, R B, Prisinzano, T E, Bohn, L M

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Cannabinoid 2 receptor- and beta Arrestin 2-dependent upregulation of serotonin 2A receptors von Franklin, J.M, Vasiljevik, T, Prisinzano, T.E, Carrasco, G.A

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The analgesic and anti‐inflammatory effects of Salvinorin A analogue β‐tetrahydropyran Salvinorin B in mice von Paton, K.F., Kumar, N., Crowley, R.S., Harper, J.L., Prisinzano, T.E., Kivell, B.M.

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Psychopharmacology of the hallucinogenic sage Salvia divinorum von Prisinzano, Thomas E.

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Pharmacology and anti‐addiction effects of the novel κ opioid receptor agonist M esyl S al B , a potent and long‐acting analogue of salvinorin A von Simonson, B, Morani, A S, Ewald, A W M, Walker, L, Kumar, N, Simpson, D, Miller, J H, Prisinzano, T E, Kivell, B M

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Effect of kappa-opioid receptor agonists U69593, U50488H, spiradoline and salvinorin A on cocaine-induced drug-seeking in rats von Morani, Aashish S., Kivell, Bronwyn, Prisinzano, Thomas E., Schenk, Susan

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Neoclerodane Diterpenes as a Novel Scaffold for μ Opioid Receptor Ligands von Harding, Wayne W, Tidgewell, Kevin, Byrd, Nathan, Cobb, Howard, Dersch, Christina M, Butelman, Eduardo R, Rothman, Richard B, Prisinzano, Thomas E

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Modafinil Alone and in Combination With Low Dose Amphetamine Does Not Establish Conditioned Place Preference in Male Sprague-Dawley Rats von Quisenberry, Amanda J., Prisinzano, Thomas E., Baker, Lisa E.

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New therapeutic potential for psychoactive natural products von Prevatt-Smith, Katherine M, Prisinzano, Thomas E

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Salvinicins A and B, new neoclerodane diterpenes from Salvia divinorum von Harding, Wayne W, Tidgewell, Kevin, Schmidt, Matthew, Shah, Kushal, Dersch, Christina M, Snyder, John, Parrish, Damon, Deschamps, Jeffrey R, Rothman, Richard B, Prisinzano, Thomas E

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Pharmacokinetics of the plant-derived κ-opioid hallucinogen salvinorin A in nonhuman primates von Schmidt, Matthew D., Schmidt, Mark S., Butelman, Eduardo R., Harding, Wayne W., Tidgewell, Kevin, Murry, Daryl J., Kreek, Mary Jeanne, Prisinzano, Thomas E.

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Determination of Salvinorin A in body fluids by high performance liquid chromatography-atmospheric pressure chemical ionization von SCHMIDT, Mark S, PRISINZANO, Thomas E, TIDGEWELL, Kevin, HARDING, Wayne, BUTELMAN, Eduardo R, KREEK, Mary J, MURRY, Daryl J

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An Opioid Agonist that Does Not Induce μ-Opioid Receptor—Arrestin Interactions or Receptor Internalization von C. E. Groer, K. Tidgewell, R. A. Moyer, W. W. Harding, R. B. Rothman, T. E. Prisinzano, L. M. Bohn

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A facile method for the preparation of deuterium labeled salvinorin A: synthesis of [2,2,2-2H3]-salvinorin A von Tidgewell, Kevin, Harding, Wayne W., Schmidt, Mark, Holden, Kenneth G., Murry, Daryl J., E. Prisinzano, Thomas

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Design and Synthesis of Promiscuous High-Affinity Monoamine Transporter Ligands:  Unraveling Transporter Selectivity von Greiner, Elisabeth, Boos, Terrence L, Prisinzano, Thomas E, De Martino, Maria G, Zeglis, Brian, Dersch, Christina M, Marcus, Jamila, Partilla, John S, Rothman, Richard B, Jacobson, Arthur E, Rice, Kenner C

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Absolute configuration of the κ-agonist salvinicin A von Deschamps, J. R., Parrish, D., Prisinzano, T. E.

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Enantioselective synthesis of (2 R,3 R)- and (2 S,3 S)-2-[(3-chlorophenyl)-(2-methoxyphenoxy)methyl]morpholine von Harding, Wayne W., Hodge, Matthis, Wang, Zhixia, Woolverton, William L., Parrish, Damon, Deschamps, Jeffrey R., Prisinzano, Thomas E.

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Advanced X-Ray Analytical Methods to Understand Structure, Properties, and Risk von Benmore, C. J.

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Diagnosing Biopharmaceutical Limitations von Jenkins, Susan M., Parker, Dawn D.

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Practical Considerations for Spray Dried Formulation and Process Development von Lowinger, Michael, Baumann, John, Vodak, David T., Moser, Justin

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