Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jessika, Klöckner"'
Autor:
Ulrike Zabel, Carsten Hoffmann, Jessika Klöckner, Susanne Nuber, Michael Kauk, Regina Messerer, Maria Consuelo Alonso Canizal, Daniela Volpato, Ulrike Holzgrabe
Publikováno v:
ACS Chemical Biology. 12:833-843
Aiming to design partial agonists as well as allosteric modulators for the M1 muscarinic acetylcholine (M1AChR) receptor, two different series of bipharmacophoric ligands and their structural analogues were designed and synthesized. The hybrids were
Autor:
Regina, Messerer, Michael, Kauk, Daniela, Volpato, Maria Consuelo, Alonso Canizal, Jessika, Klöckner, Ulrike, Zabel, Susanne, Nuber, Carsten, Hoffmann, Ulrike, Holzgrabe
Publikováno v:
ACS chemical biology. 12(3)
Aiming to design partial agonists as well as allosteric modulators for the M
Autor:
Clelia Dallanoce, Evi Kostenis, Klaus Mohr, M. De Amici, Jessika Klöckner, Ulrike Holzgrabe, Wiebke K. Seemann, Ramona Schrage, Kurt Racké
Publikováno v:
British Journal of Pharmacology. 169:357-370
Background and Purpose Artificial agonists may have higher efficacy for receptor activation than the physiological agonist. Until now, such ‘superagonism’ has rarely been reported for GPCRs. Iperoxo is an extremely potent muscarinic receptor agon
Autor:
Christian Tränkle, Jessika Klöckner, Klaus Mohr, Andreas Bock, Michael Decker, Wiebke K. Seemann, Cornelia Zimmermann, Ulrike Holzgrabe, Ramona Schrage, Janine Holze, Xinyu Chen
Publikováno v:
Journal of medicinal chemistry. 58(2)
Aiming to design partial agonists for a G-protein-coupled receptor based on dynamic ligand binding, we synthesized three different series of bipharmacophoric ligands composed of the orthosteric building blocks iperoxo and 1 linked to allosteric modul