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Showing results (61-70 of 96) with videos related to

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Bioorganic & Medicinal Chemistry Letters|January 5, 2002
Synthesis and structure-activity relationships of oxime neurokinin antagonists: discovery of potent arylamidesNeng Yang Shih, Margaret Albanese, John C Anthes, et al.
European Journal of Pharmacology|May 24, 2008
In-vitro and in-vivo characterization of JNJ-7925476, a novel triple monoamine uptake inhibitorLeah Aluisio, Brian Lord, Ann J Barbier, et al.
Bioorganic & Medicinal Chemistry Letters|February 24, 2007
Pyrrolidino-tetrahydroisoquinolines as potent dual H3 antagonist and serotonin transporter inhibitorsJohn M Keith, Leslie A Gomez, Ronald L Wolin, et al.
ACS Medicinal Chemistry Letters|March 21, 2019
1<i>H</i>-Pyrrolo[3,2-<i>b</i>]pyridine GluN2B-Selective Negative Allosteric ModulatorsChrista C Chrovian, Akinola Soyode-Johnson, Jessica L Wall, et al.
Bioorganic & Medicinal Chemistry Letters|January 3, 2009
Novel imidazole-based histamine H3 antagonistsJill A Jablonowski, Kiev S Ly, Michael Bogenstaetter, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 14, 2009
Blockade of orexin-1 receptors attenuates orexin-2 receptor antagonism-induced sleep promotion in the ratChristine Dugovic, Jonathan E Shelton, Leah E Aluisio, et al.
Bioorganic & Medicinal Chemistry Letters|September 17, 2010
Indole- and benzothiophene-based histamine H3 antagonistsAlejandro Santillan, Kelly J McClure, Brett D Allison, et al.
ACS Medicinal Chemistry Letters|March 21, 2019
Discovery of Imidazo[1,2-<i>a</i>]pyrazines and Pyrazolo[1,5-<i>c</i>]pyrimidines as TARP γ-8 Selective AMPAR Negative ModulatorsBrad M Savall, Dongpei Wu, Devin M Swanson, et al.
British Journal of Pharmacology|October 7, 2004
Acute wake-promoting actions of JNJ-5207852, a novel, diamine-based H3 antagonistA J Barbier, C Berridge, C Dugovic, et al.
Nuclear Medicine and Biology|August 29, 2006
Radiosynthesis and biodistribution of a histamine H3 receptor antagonist 4-[3-(4-piperidin-1-yl-but-1-ynyl)-[11C]benzyl]-morpholine: evaluation of a potential PET ligandAnu J Airaksinen, Jill A Jablonowski, Margreet van der Mey, et al.
Pageof 10

Showing results (61-70 of 96) with videos related to

Sort By:
Pageof 10
Bioorganic & Medicinal Chemistry Letters|January 5, 2002
Synthesis and structure-activity relationships of oxime neurokinin antagonists: discovery of potent arylamidesNeng Yang Shih, Margaret Albanese, John C Anthes, et al.
European Journal of Pharmacology|May 24, 2008
In-vitro and in-vivo characterization of JNJ-7925476, a novel triple monoamine uptake inhibitorLeah Aluisio, Brian Lord, Ann J Barbier, et al.
Bioorganic & Medicinal Chemistry Letters|February 24, 2007
Pyrrolidino-tetrahydroisoquinolines as potent dual H3 antagonist and serotonin transporter inhibitorsJohn M Keith, Leslie A Gomez, Ronald L Wolin, et al.
ACS Medicinal Chemistry Letters|March 21, 2019
1<i>H</i>-Pyrrolo[3,2-<i>b</i>]pyridine GluN2B-Selective Negative Allosteric ModulatorsChrista C Chrovian, Akinola Soyode-Johnson, Jessica L Wall, et al.
Bioorganic & Medicinal Chemistry Letters|January 3, 2009
Novel imidazole-based histamine H3 antagonistsJill A Jablonowski, Kiev S Ly, Michael Bogenstaetter, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 14, 2009
Blockade of orexin-1 receptors attenuates orexin-2 receptor antagonism-induced sleep promotion in the ratChristine Dugovic, Jonathan E Shelton, Leah E Aluisio, et al.
Bioorganic & Medicinal Chemistry Letters|September 17, 2010
Indole- and benzothiophene-based histamine H3 antagonistsAlejandro Santillan, Kelly J McClure, Brett D Allison, et al.
ACS Medicinal Chemistry Letters|March 21, 2019
Discovery of Imidazo[1,2-<i>a</i>]pyrazines and Pyrazolo[1,5-<i>c</i>]pyrimidines as TARP γ-8 Selective AMPAR Negative ModulatorsBrad M Savall, Dongpei Wu, Devin M Swanson, et al.
British Journal of Pharmacology|October 7, 2004
Acute wake-promoting actions of JNJ-5207852, a novel, diamine-based H3 antagonistA J Barbier, C Berridge, C Dugovic, et al.
Nuclear Medicine and Biology|August 29, 2006
Radiosynthesis and biodistribution of a histamine H3 receptor antagonist 4-[3-(4-piperidin-1-yl-but-1-ynyl)-[11C]benzyl]-morpholine: evaluation of a potential PET ligandAnu J Airaksinen, Jill A Jablonowski, Margreet van der Mey, et al.
Pageof 10