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International Journal of Molecular Sciences|August 27, 2021
Optimizing the Expression of Human Dopamine Receptors in <i>Escherichia coli</i>Vanessa Boritzki, Harald Hübner, Anni Allikalt, et al.Journal of Medicinal Chemistry|September 2, 2005
Pharmacophore-guided drug discovery investigations leading to bioactive 5-aminotetrahydropyrazolopyridines. Implications for the binding mode of heterocyclic dopamine D3 receptor agonistsJan Elsner, Frank Boeckler, Frank W Heinemann, et al.The Journal of Physical Chemistry. B|December 1, 2006
SCRF-DFT and NMR comparison of tetracycline and 5a,6-anhydrotetracycline in solutionOlaf G Othersen, Reiner Waibel, Harald Lanig, et al.Biochemistry|July 21, 2004
Structure-based design of Tet repressor to optimize a new inducer specificityEva-Maria Henssler, Oliver Scholz, Susanne Lochner, et al.Bioorganic & Medicinal Chemistry|August 25, 2015
1,4-Disubstituted aromatic piperazines with high 5-HT2A/D2 selectivity: Quantitative structure-selectivity investigations, docking, synthesis and biological evaluationDorothee Möller, Ismail Salama, Ralf C Kling, et al.Addiction Biology|January 25, 2021
Sensitization to amphetamine psychostimulant effect: A key role for ventral tegmental area neurotensin type 2 receptors and MAP kinase pathwayDavid Voyer, Jürgen Einsiedel, Peter Gmeiner, et al.The Journal of Organic Chemistry|March 28, 2008
Proline derived spirobarbiturates as highly effective beta-turn mimetics incorporating polar and functionalizable constraint elementsLuelak Lomlim, Juergen Einsiedel, Frank W Heinemann, et al.Plos One|June 17, 2014
Active-state model of a dopamine D2 receptor-Gαi complex stabilized by aripiprazole-type partial agonistsRalf C Kling, Nuska Tschammer, Harald Lanig, et al.Bioorganic & Medicinal Chemistry Letters|July 1, 2004
Synthesis and radioiodination of selective ligands for the dopamine D3 receptor subtypeCarsten Hocke, Olaf Prante, Stefan Löber, et al.Bioorganic & Medicinal Chemistry Letters|September 3, 2003
Stereocontrolled dopamine receptor binding and subtype selectivity of clebopride analogues synthesized from aspartic acidJürgen Einsiedel, Klaus Weber, Christoph Thomas, et al.Pageof 25