Petrine Wellendorph
Affiliations: | Biomedicine | University of Basel, Basel, Basel-Stadt, Switzerland |
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| Łątka K, Kickinger S, Rzepka Z, et al. (2024) Rational Search for Betaine/GABA Transporter 1 Inhibitors─ Evaluation of Selected Hit Compound. Acs Chemical Neuroscience. 15: 4046-4054 |
| Mitsui K, Lie MEK, Saito N, et al. (2022) Synthesis of γ-Aminobutyric Acid (GABA) Analogues Conformationally Restricted by Bicyclo[3.1.0]hexane/hexene or [4.1.0]Heptane/heptene Backbones as Potent Betaine/GABA Transporter Inhibitors. Organic Letters. 24: 4151-4154 |
| Khumpirapang N, Suknuntha K, Wongrattanakamon P, et al. (2022) The Binding of Oil and Its Nanoemulsion to Mammal GABA Receptors Using Rat Cortical Membranes and an In Silico Modeling Platform. Pharmaceutics. 14 |
| Bavo F, de-Jong H, Petersen J, et al. (2021) Structure-Activity Studies of 3,9-Diazaspiro[5.5]undecane-Based γ-Aminobutyric Acid Type A Receptor Antagonists with Immunomodulatory Effect. Journal of Medicinal Chemistry |
| Kickinger S, Lie MEK, Suemasa A, et al. (2021) Molecular Determinants and Pharmacological Analysis for a Class of Competitive Non-transported Bicyclic Inhibitors of the Betaine/GABA Transporter BGT1. Frontiers in Chemistry. 9: 736457 |
| Falk-Petersen CB, Rostrup F, Löffler R, et al. (2021) δ. Molecular Pharmacology |
| Rostrup F, Falk-Petersen CB, Harpso E K, et al. (2021) Structural Determinants for the Mode of Action of Imidazopyridine DS2 at δ-Containing γ-Aminobutyric Acid Type A Receptors. Journal of Medicinal Chemistry |
| Kickinger S, Al-Khawaja A, Haugaard AS, et al. (2020) Exploring the molecular determinants for subtype-selectivity of 2-amino-1,4,5,6-tetrahydropyrimidine-5-carboxylic acid analogs as betaine/GABA transporter 1 (BGT1) substrate-inhibitors. Scientific Reports. 10: 12992 |
| Andersen JV, Jakobsen E, Westi EW, et al. (2020) Extensive astrocyte metabolism of γ-aminobutyric acid (GABA) sustains glutamine synthesis in the mammalian cerebral cortex. Glia |
| Falk-Petersen CB, Tsonkov TM, Nielsen MS, et al. (2020) Discovery of a new class of orthosteric antagonists with nanomolar potency at extrasynaptic GABA receptors. Scientific Reports. 10: 10078 |