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Gábor Wágner

Showing results (1-10 of 14) with videos related to

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Biochemical and Biophysical Research Communications|September 19, 2003
Glucose conversion by multiple pathways in brain extract: theoretical and experimental analysisFerenc Orosz, Gábor Wágner, Fernando Ortega, et al.
Bioorganic & Medicinal Chemistry Letters|August 7, 2016
Charting the chemical space around the (iso)indoline scaffold, a comprehensive approach towards multitarget directed ligandsOlivér Éliás, Zoltán Kovács, Gábor Wágner, et al.
Current Topics in Behavioral Neurosciences|July 19, 2022
New Chemical Biology Tools for the Histamine Receptor FamilyYang Zheng, Gábor Wágner, Niels Hauwert, et al.
Molecules (Basel, Switzerland)|February 25, 2023
Green Drug Discovery: Novel Fragment Space from the Biomass-Derived Molecule Dihydrolevoglucosenone (Cyrene<sup>TM</sup>)Tom Dekker, Jaap W Harteveld, Gábor Wágner, et al.
Molecules (Basel, Switzerland)|December 15, 2019
Covalent Inhibition of the Histamine H<sub>3</sub> ReceptorGábor Wágner, Tamara A M Mocking, Albert J Kooistra, et al.
Bioorganic & Medicinal Chemistry Letters|July 15, 2014
Thieno[2,3-b]pyridines as negative allosteric modulators of metabotropic GluR5 receptors: hit-to-lead optimizationKatalin Nógrádi, Gábor Wágner, György Domány, et al.
Bioorganic & Medicinal Chemistry Letters|March 21, 2015
Thieno[2,3-b]pyridines as negative allosteric modulators of metabotropic GluR5 receptors: Lead optimizationKatalin Nógrádi, Gábor Wágner, György Domány, et al.
Bioorganic & Medicinal Chemistry Letters|January 18, 2016
4-Aryl-3-arylsulfonyl-quinolines as negative allosteric modulators of metabotropic GluR5 receptors: From HTS hit to development candidateJános Galambos, György Domány, Katalin Nógrádi, et al.
Bioorganic & Medicinal Chemistry Letters|May 21, 2010
Hit-to-lead optimization of disubstituted oxadiazoles and tetrazoles as mGluR5 NAMsGábor Wágner, Csaba Wéber, Olga Nyéki, et al.
Journal of Medicinal Chemistry|November 2, 2019
4-(3-Aminoazetidin-1-yl)pyrimidin-2-amines as High-Affinity Non-imidazole Histamine H<sub>3</sub> Receptor Agonists with in Vivo Central Nervous System ActivityGábor Wágner, Tamara A M Mocking, Marta Arimont, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Biochemical and Biophysical Research Communications|September 19, 2003
Glucose conversion by multiple pathways in brain extract: theoretical and experimental analysisFerenc Orosz, Gábor Wágner, Fernando Ortega, et al.
Bioorganic & Medicinal Chemistry Letters|August 7, 2016
Charting the chemical space around the (iso)indoline scaffold, a comprehensive approach towards multitarget directed ligandsOlivér Éliás, Zoltán Kovács, Gábor Wágner, et al.
Current Topics in Behavioral Neurosciences|July 19, 2022
New Chemical Biology Tools for the Histamine Receptor FamilyYang Zheng, Gábor Wágner, Niels Hauwert, et al.
Molecules (Basel, Switzerland)|February 25, 2023
Green Drug Discovery: Novel Fragment Space from the Biomass-Derived Molecule Dihydrolevoglucosenone (Cyrene<sup>TM</sup>)Tom Dekker, Jaap W Harteveld, Gábor Wágner, et al.
Molecules (Basel, Switzerland)|December 15, 2019
Covalent Inhibition of the Histamine H<sub>3</sub> ReceptorGábor Wágner, Tamara A M Mocking, Albert J Kooistra, et al.
Bioorganic & Medicinal Chemistry Letters|July 15, 2014
Thieno[2,3-b]pyridines as negative allosteric modulators of metabotropic GluR5 receptors: hit-to-lead optimizationKatalin Nógrádi, Gábor Wágner, György Domány, et al.
Bioorganic & Medicinal Chemistry Letters|March 21, 2015
Thieno[2,3-b]pyridines as negative allosteric modulators of metabotropic GluR5 receptors: Lead optimizationKatalin Nógrádi, Gábor Wágner, György Domány, et al.
Bioorganic & Medicinal Chemistry Letters|January 18, 2016
4-Aryl-3-arylsulfonyl-quinolines as negative allosteric modulators of metabotropic GluR5 receptors: From HTS hit to development candidateJános Galambos, György Domány, Katalin Nógrádi, et al.
Bioorganic & Medicinal Chemistry Letters|May 21, 2010
Hit-to-lead optimization of disubstituted oxadiazoles and tetrazoles as mGluR5 NAMsGábor Wágner, Csaba Wéber, Olga Nyéki, et al.
Journal of Medicinal Chemistry|November 2, 2019
4-(3-Aminoazetidin-1-yl)pyrimidin-2-amines as High-Affinity Non-imidazole Histamine H<sub>3</sub> Receptor Agonists with in Vivo Central Nervous System ActivityGábor Wágner, Tamara A M Mocking, Marta Arimont, et al.
Pageof 2