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ACS Chemical Neuroscience|February 27, 2016
Concise Asymmetric Synthesis and Pharmacological Characterization of All Stereoisomers of Glutamate Transporter Inhibitor TFB-TBOA and Synthesis of EAAT Photoaffinity ProbesMichele Leuenberger, Andreas Ritler, Alexandre Simonin, et al.
The Journal of Pharmacology and Experimental Therapeutics|March 30, 2021
Characterization of Novel Fluorescent Bile Salt Derivatives for Studying Human Bile Salt and Organic Anion TransportersMichele Leuenberger, Stephanie Häusler, Vera Höhn, et al.
Neuropharmacology|February 1, 2017
The binding orientations of structurally-related ligands can differ; A cautionary noteMarc-David Ruepp, Hao Wei, Michele Leuenberger, et al.
Journal of Inorganic Biochemistry|March 19, 2002
A supramolecular enzyme model catalyzing the central cleavage of carotenoidsRichard R French, Philipp Holzer, Michele Leuenberger, et al.
Bioorganic & Medicinal Chemistry|April 23, 2013
Design, synthesis and pharmacological characterization of analogs of 2-aminoethyl diphenylborinate (2-APB), a known store-operated calcium channel blocker, for inhibition of TRPV6-mediated calcium transportAlexandre Hofer, Gergely Kovacs, Anna Zappatini, et al.
Molecular Aspects of Medicine|March 20, 2013
The SLC1 high-affinity glutamate and neutral amino acid transporter familyYoshikatsu Kanai, Benjamin Clémençon, Alexandre Simonin, et al.
ACS Pharmacology & Translational Science|February 22, 2021
Deciphering the Agonist Binding Mechanism to the Adenosine A1 ReceptorGiuseppe Deganutti, Kerry Barkan, Barbara Preti, et al.
Journal of Medicinal Chemistry|October 21, 2022
Discovery and Structure-Activity Relationship Studies of Novel Adenosine A<sub>1</sub> Receptor-Selective AgonistsBarbara Preti, Anna Suchankova, Giuseppe Deganutti, et al.
Journal of Medicinal Chemistry|January 13, 2016
Discovery of Novel Adenosine Receptor Agonists That Exhibit Subtype SelectivityAnthony Knight, Jennifer L Hemmings, Ian Winfield, et al.
ACS Chemical Neuroscience|August 29, 2018
Mapping the Orthosteric Binding Site of the Human 5-HT<sub>3</sub> Receptor Using Photo-cross-linking AntagonistsThomas Jack, Michele Leuenberger, Marc-David Ruepp, et al.
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