19 articles for thisTarget
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A binding mode hypothesis of tiagabine confirms liothyronine effect on¿-aminobutyric acid transporter 1 (GAT1).

University of Vienna
A binary QSAR model for classification of hERG potassium channel blockers.

University of Vienna
Self-organizing maps for identification of new inhibitors of P-glycoprotein.

University of Vienna
Substituted 4-acylpyrazoles and 4-acylpyrazolones: synthesis and multidrug resistance-modulating activity.

University of Vienna
Modulation of GABAA-receptors by honokiol and derivatives: subtype selectivity and structure-activity relationship.

University of Vienna
Bioactivity-guided isolation of 1,2,3,4,6-Penta-O-galloyl-D-glucopyranose from Paeonia lactiflora roots as a PTP1B inhibitor.

University of Vienna
'Bridged' stilbene derivatives as selective cyclooxygenase-1 inhibitors.

University of Vienna
Flindissone, a Limonoid Isolated from

University of Vienna
Novel alpha6 preferring GABA-A receptor ligands based on loreclezole.

University of Vienna
Identification of Natural Products Inhibiting SARS-CoV-2 by Targeting Viral Proteases: A Combined in Silico and in Vitro Approach.

University of Vienna
Polyacetylenes from

University of Vienna
Structure-Activity Relationships of Novel Thiazole-Based Modafinil Analogues Acting at Monoamine Transporters.

University of Vienna
Design, Synthesis, and Pharmacological Evaluation of Novel β2/3 Subunit-Selective γ-Aminobutyric Acid Type A (GABA

University of Vienna
Efficient modulation of γ-aminobutyric acid type A receptors by piperine derivatives.

University of Vienna
Structure-activity relationships, ligand efficiency, and lipophilic efficiency profiles of benzophenone-type inhibitors of the multidrug transporter P-glycoprotein.

University of Vienna
Ligand Desolvation Steers On-Rate and Impacts Drug Residence Time of Heat Shock Protein 90 (Hsp90) Inhibitors.

University of Vienna
Heterocyclic Analogues of Modafinil as Novel, Atypical Dopamine Transporter Inhibitors.

University of Vienna
Direct NMR Probing of Hydration Shells of Protein Ligand Interfaces and Its Application to Drug Design.

University of Vienna