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Bioorganic & Medicinal Chemistry|September 11, 2007
Click chemistry based solid phase supported synthesis of dopaminergic phenylacetylenesPilar Rodriguez Loaiza, Stefan Löber, Harald Hübner, et al.
Bioorganic & Medicinal Chemistry|June 2, 2009
Design, synthesis and dopamine D4 receptor binding activities of new N-heteroaromatic 5/6-ring Mannich basesSabine Linz, Jörg Müller, Harald Hübner, et al.
Scientific Reports|January 23, 2020
Structure-based development of caged dopamine D<sub>2</sub>/D<sub>3</sub> receptor antagonistsMarie Gienger, Harald Hübner, Stefan Löber, et al.
Journal of Medicinal Chemistry|June 24, 2016
(18)F- and (68)Ga-Labeled Neurotensin Peptides for PET Imaging of Neurotensin Receptor 1Simone Maschauer, Jürgen Einsiedel, Harald Hübner, et al.
Chemmedchem|October 11, 2023
Development of Photoswitchable Tethered Ligands that Target the μ-Opioid ReceptorRanit Lahmy, Harald Hübner, Daniel Lachmann, et al.
Bioorganic & Medicinal Chemistry|December 8, 2004
Fancy bioisosteres: synthesis and dopaminergic properties of the endiyne FAUC 88 as a novel non-aromatic D3 agonistCarola Lenz, Christian Haubmann, Harald Hübner, et al.
Bioorganic & Medicinal Chemistry Letters|October 9, 2013
Click chemistry based synthesis of dopamine D4 selective receptor ligands for the selection of potential PET tracersAshutosh Banerjee, Simone Maschauer, Harald Hübner, et al.
Journal of Medicinal Chemistry|October 7, 2008
Novel D3 selective dopaminergics incorporating enyne units as nonaromatic catechol bioisosteres: synthesis, bioactivity, and mutagenesis studiesMiriam Dörfler, Nuska Tschammer, Katharina Hamperl, et al.
Scientific Reports|September 9, 2017
Visualization of ligand-induced dopamine D<sub>2S</sub> and D<sub>2L</sub> receptor internalization by TIRF microscopyAlina Tabor, Dorothee Möller, Harald Hübner, et al.
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