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Bioorganic & Medicinal Chemistry|March 25, 2022
Development of disulfide-functionalized peptides covalently binding G protein-coupled receptorsJürgen Einsiedel, Maximilian F Schmidt, Harald Hübner, et al.Journal of Combinatorial Chemistry|March 15, 2006
Click chemistry on solid phase: parallel synthesis of N-benzyltriazole carboxamides as super-potent G-protein coupled receptor ligandsPilar Rodriguez Loaiza, Stefan Löber, Harald Hübner, et al.Bioorganic & Medicinal Chemistry Letters|February 15, 2002
Di- and trisubstituted pyrazolo[1,5-a]pyridine derivatives: synthesis, dopamine receptor binding and ligand efficacyStefan Löber, Tarek Aboul-Fadl, Harald Hübner, 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.Journal of Medicinal Chemistry|October 27, 2006
A chimeric ligand approach leading to potent antiprion active acridine derivatives: design, synthesis, and biological investigationsSilke Dollinger, Stefan Löber, Ralf Klingenstein, 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.Organic Letters|June 11, 2011
A highly efficient type I β-turn mimetic simulating an Asx-Pro-turn-like structureAndrea Pinsker, Jürgen Einsiedel, Steffen Härterich, 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.Chembiochem : a European Journal of Chemical Biology|February 12, 2010
Click-chemistry-derived tetracycline-amino acid conjugates exhibiting exceptional potency and exclusive recognition of the reverse tet repressorIgor Usai, Marcus Krueger, Jürgen Einsiedel, et al.Bioorganic & Medicinal Chemistry|November 18, 2005
Bicyclic melatonin receptor agonists containing a ring-junction nitrogen: Synthesis, biological evaluation, and molecular modeling of the putative bioactive conformationJan Elsner, Frank Boeckler, Kathryn Davidson, et al.Pageof 25