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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 ReceptorsLouisa Temme, Dirk Schepmann, Julian A Schreiber, et al.
Medchemcomm|August 16, 2018
Do GluN2B subunit containing NMDA receptors tolerate a fluorine atom in the phenylalkyl side chain?Yoshihiro Shuto, Simone Thum, Louisa Temme, et al.
European Journal of Medicinal Chemistry|January 1, 2018
Hydroxymethyl bioisosteres of phenolic GluN2B-selective NMDA receptor antagonists: Design, synthesis and pharmacological evaluationLouisa Temme, Bastian Frehland, Dirk Schepmann, et al.
Bioorganic & Medicinal Chemistry|October 26, 2019
Impact of hydroxy moieties at the benzo[7]annulene ring system of GluN2B ligands: Design, synthesis and biological evaluationLouisa Temme, Frederik Börgel, Dirk Schepmann, et al.
European Journal of Medicinal Chemistry|February 20, 2020
Negative allosteric modulators of the GluN2B NMDA receptor with phenylethylamine structure embedded in ring-expanded and ring-contracted scaffoldsLouisa Temme, Elena Bechthold, Julian A Schreiber, et al.
European Journal of Medicinal Chemistry|July 14, 2017
Deconstruction - reconstruction approach to analyze the essential structural elements of tetrahydro-3-benzazepine-based antagonists of GluN2B subunit containing NMDA receptorsSougata Dey, Louisa Temme, Julian A Schreiber, et al.
Chemmedchem|March 29, 2014
GluN2B-selective N-methyl-D-aspartate (NMDA) receptor antagonists derived from 3-benzazepines: synthesis and pharmacological evaluation of benzo[7]annulen-7-aminesAndre Benner, Alessandro Bonifazi, Chikako Shirataki, et al.
Chemmedchem|July 28, 2017
Design, Synthesis, Pharmacological Evaluation and Docking Studies of GluN2B-Selective NMDA Receptor Antagonists with a Benzo[7]annulen-7-amine ScaffoldSandeep Gawaskar, Louisa Temme, Julian A Schreiber, et al.
British Journal of Pharmacology|February 27, 2025
Chemosensory signalling in human sperm is controlled by Ca2+ influx via CatSper and Ca2+ clearance via plasma membrane Ca2+ ATPasesLeonie Herrmann, Christoph Brenker, Teresa Mittermair, et al.
Chemmedchem|May 29, 2018
Synthesis and Pharmacological Evaluation of Enantiomerically Pure GluN2B Selective NMDA Receptor AntagonistsFrederik Börgel, Marina Szermerski, Julian A Schreiber, et al.
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