Anzahl der Einträge: 5.
Artikel
Dukorn, Stefanie,
Littmann, Timo,
Keller, Max,
Kuhn, Kilian K.,
Cabrele, Chiara ,
Baumeister, Paul,
Bernhardt, Günther und
Buschauer, Armin
(2017)
Fluorescence- and radio-labeling of Lys4,Nle17,30hPP yields molecular tools for the NPY Y4 receptor.
Bioconjugate Chemistry.
Volltext nicht vorhanden.
Kuhn, Kilian K.,
Littmann, Timo,
Dukorn, Stefanie,
Tanaka, Miho,
Keller, Max,
Ozawa, Takeaki,
Bernhardt, Günther und
Buschauer, Armin
(2017)
In Search of NPY Y4R Antagonists: Incorporation of Carbamoylated Arginine, Aza-Amino Acids, or d-Amino Acids into Oligopeptides Derived from the C-Termini of the Endogenous Agonists.
ACS Omega 2 (7), S. 3616-3631.
Kuhn, Kilian K.,
Ertl, Thomas,
Dukorn, Stefanie,
Keller, Max,
Bernhardt, Günther,
Reiser, Oliver und
Buschauer, Armin
(2016)
High affinity agonists of the neuropeptide Y (NPY) Y4 receptor derived from the C-terminal pentapeptide of human pancreatic polypeptide (hPP): synthesis, stereochemical discrimination and radiolabeling.
Journal of Medicinal Chemistry 59 (13), S. 6045-6058.
Volltext nicht vorhanden.
Keller, Max,
Kuhn, Kilian K.,
Einsiedel, Jürgen,
Hübner, Harald,
Biselli, Sabrina,
Mollereau, Catherine ,
Wifling, David,
Svobodova, Jaroslava,
Bernhardt, Günther,
Cabrele, Chiara ,
Vanderheyden, Patrick,
Gmeiner, Peter und
Buschauer, Armin
(2016)
Mimicking of arginine by functionalized Nω-carbamoylated arginine as a new broadly applicable approach to labeled bioactive peptides: high affinity angiotensin, neuropeptide Y, neuropeptide FF and neurotensin receptor ligands as examples.
Journal of Medicinal Chemistry 59 (5), S. 1925-1945.
Volltext nicht vorhanden.
Keller, Max,
Weiss, Stefan,
Hutzler, Christoph,
Kuhn, Kilian K.,
Mollereau, Catherine,
Dukorn, Stefanie,
Schindler, Lisa,
Bernhardt, Günther,
König, Burkhard und
Buschauer, Armin
(2015)
N(omega)-carbamoylation of the argininamide moiety: an avenue to insurmountable NPY Y1 receptor antagonists and a radiolabeled selective high affinity molecular tool ([3H]UR-MK299) with extended residence time.
Journal of Medicinal Chemistry 58 (22), S. 8834-8849.
Volltext nicht vorhanden.
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