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Advances in Experimental Medicine and Biology
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January 28, 2026
Structure-Function Relationships of K<sub>2P</sub> Channels
Julian A Schreiber, Guiscard Seebohm
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology
|
May 27, 2021
Beyond Hot and Spicy: TRPV Channels and their Pharmacological Modulation
Guiscard Seebohm, Julian A Schreiber
Handbook of Experimental Pharmacology
|
July 11, 2021
Cardiac K<sup>+</sup> Channels and Channelopathies
Julian A Schreiber, Guiscard Seebohm
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology
|
November 25, 2022
The Special One: Architecture, Physiology and Pharmacology of the TRESK Channel
Julian A Schreiber, Martina Düfer, Guiscard Seebohm
Chemmedchem
|
January 30, 2018
Comparative Pharmacological Study of Common NMDA Receptor Open Channel Blockers Regarding Their Affinity and Functional Activity toward GluN2A and GluN2B NMDA Receptors
Louisa Temme, Dirk Schepmann, Julian A Schreiber, et al.
European Journal of Medicinal Chemistry
|
November 9, 2020
Synthesis of GluN2A-selective NMDA receptor antagonists with an electron-rich aromatic B-ring
Remya Rajan, Dirk Schepmann, Julian A Schreiber, et al.
Journal of Medicinal Chemistry
|
December 30, 2025
Stereoselective Synthesis of Conformationally Restricted γ- and β-Amino Alcohols as GluN2B Subtype-Selective NMDA Receptor Antagonists
Marvin Korff, Gunnar Goerges, Judith Schmidt, et al.
European Journal of Medicinal Chemistry
|
April 25, 2022
Synthesis and biological evaluation of conformationally restricted GluN2B ligands derived from eliprodil
Elena Bechthold, Julian A Schreiber, Nadine Ritter, et al.
Archiv Der Pharmazie
|
May 23, 2022
Phenol-Benzoxazolone bioisosteres: Synthesis and biological evaluation of tricyclic GluN2B-selective N-methyl- d-aspartate receptor antagonists
Alexander Markus, Julian A Schreiber, Gunnar Goerges, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology
|
March 3, 2021
Deconstruction - Reconstruction: Analysis of the Crucial Structural Elements of GluN2B-Selective, Negative Allosteric NMDA Receptor Modulators with 3-Benzazepine Scaffold
Nadine Ritter, Marvin Korff, Alexander Markus, et al.
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Search research articles
Search
Showing results (1-10 of 35) with videos related to
Sort By:
Page
of 4
Advances in Experimental Medicine and Biology
|
January 28, 2026
Structure-Function Relationships of K<sub>2P</sub> Channels
Julian A Schreiber, Guiscard Seebohm
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology
|
May 27, 2021
Beyond Hot and Spicy: TRPV Channels and their Pharmacological Modulation
Guiscard Seebohm, Julian A Schreiber
Handbook of Experimental Pharmacology
|
July 11, 2021
Cardiac K<sup>+</sup> Channels and Channelopathies
Julian A Schreiber, Guiscard Seebohm
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology
|
November 25, 2022
The Special One: Architecture, Physiology and Pharmacology of the TRESK Channel
Julian A Schreiber, Martina Düfer, Guiscard Seebohm
Chemmedchem
|
January 30, 2018
Comparative Pharmacological Study of Common NMDA Receptor Open Channel Blockers Regarding Their Affinity and Functional Activity toward GluN2A and GluN2B NMDA Receptors
Louisa Temme, Dirk Schepmann, Julian A Schreiber, et al.
European Journal of Medicinal Chemistry
|
November 9, 2020
Synthesis of GluN2A-selective NMDA receptor antagonists with an electron-rich aromatic B-ring
Remya Rajan, Dirk Schepmann, Julian A Schreiber, et al.
Journal of Medicinal Chemistry
|
December 30, 2025
Stereoselective Synthesis of Conformationally Restricted γ- and β-Amino Alcohols as GluN2B Subtype-Selective NMDA Receptor Antagonists
Marvin Korff, Gunnar Goerges, Judith Schmidt, et al.
European Journal of Medicinal Chemistry
|
April 25, 2022
Synthesis and biological evaluation of conformationally restricted GluN2B ligands derived from eliprodil
Elena Bechthold, Julian A Schreiber, Nadine Ritter, et al.
Archiv Der Pharmazie
|
May 23, 2022
Phenol-Benzoxazolone bioisosteres: Synthesis and biological evaluation of tricyclic GluN2B-selective N-methyl- d-aspartate receptor antagonists
Alexander Markus, Julian A Schreiber, Gunnar Goerges, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology
|
March 3, 2021
Deconstruction - Reconstruction: Analysis of the Crucial Structural Elements of GluN2B-Selective, Negative Allosteric NMDA Receptor Modulators with 3-Benzazepine Scaffold
Nadine Ritter, Marvin Korff, Alexander Markus, et al.
Page
of 4