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Published in Current protocols in pharmacology (01.09.2016)
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Glycine transporter (GlyT1) inhibitors with reduced residence time increase prepulse inhibition without inducing hyperlocomotion in DBA/2 mice
Kopec, Karla, Flood, Dorothy G., Gasior, Maciej, McKenna, Beth Ann W., Zuvich, Eva, Schreiber, Justin, Salvino, Joseph M., Durkin, John T., Ator, Mark A., Marino, Michael J.
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Published in Biochemical pharmacology (01.11.2010)
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Reductions in log P Improved Protein Binding and Clearance Predictions Enabling the Prospective Design of Cannabinoid Receptor (CB1) Antagonists with Desired Pharmacokinetic Properties
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Published in Journal of medicinal chemistry (12.12.2013)
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Discovery of ( R )-9-Ethyl-1,3,4,10b-tetrahydro-7-trifluoromethylpyrazino[2,1- a ]isoindol- 6(2 H )-one, a Selective, Orally Active Agonist of the 5-HT 2C Receptor
Wacker, Dean A., Varnes, Jeffrey G., Malmstrom, Sarah E., Cao, Xueying, Hung, Chen-Pin, Ung, Thao, Wu, Ginger, Zhang, Ge, Zuvich, Eva, Thomas, Michael A., Keim, William J., Cullen, Mary Jane, Rohrbach, Kenneth W., Qu, Qinling, Narayanan, Rangaraj, Rossi, Karen, Janovitz, Evan, Lehman-McKeeman, Lois, Malley, Mary F., Devenny, James, Pelleymounter, Mary Ann, Miller, Keith J., Robl, Jeffrey A.
Published in Journal of medicinal chemistry (22.03.2007)
Published in Journal of medicinal chemistry (22.03.2007)
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Discovery of (R)-9-Ethyl-1,3,4,10b-tetrahydro-7-trifluoromethylpyrazino[2,1-a]isoindol- 6(2H)-one, a Selective, Orally Active Agonist of the 5-HT2C Receptor
Wacker, Dean A, Varnes, Jeffrey G, Malmstrom, Sarah E, Cao, Xueying, Hung, Chen-Pin, Ung, Thao, Wu, Ginger, Zhang, Ge, Zuvich, Eva, Thomas, Michael A, Keim, William J, Cullen, Mary Jane, Rohrbach, Kenneth W, Qu, Qinling, Narayanan, Rangaraj, Rossi, Karen, Janovitz, Evan, Lehman-McKeeman, Lois, Malley, Mary F, Devenny, James, Pelleymounter, Mary Ann, Miller, Keith J, Robl, Jeffrey A
Published in Journal of medicinal chemistry (22.03.2007)
Published in Journal of medicinal chemistry (22.03.2007)
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Discovery of (R)-9-ethyl-1,3,4,10b-tetrahydro-7-trifluoromethylpyrazino[2,1-a]isoindol- 6(2H)-one, a selective, orally active agonist of the 5-HT(2C) receptor
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Published in Journal of medicinal chemistry (22.03.2007)
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Published in Journal of medicinal chemistry (22.03.2007)
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