Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Michaela Prinz"'
Autor:
Adyary Fallarero, Gulsah Bayraktar, Pia Vuorela, Carola Schiller, Ezgi Turunc, Manuel Krug, Sülünay Parlar, Guliz Armagan, Ayfer Yalcin, Vildan Alptüzün, Christoph A. Sotriffer, Kristina Leuner, Daniela Karlsson, Malgorzata Burek, Michaela Prinz, Ulrike Holzgrabe, Ercin Erciyas, Carola Förster
Publikováno v:
European Journal of Pharmaceutical Sciences. 49:603-613
Given the fundamentally multifactorial character of Alzheimer's disease (AD), addressing more than one target for disease modification or therapy is expected to be highly advantageous. Here, following the cholinergic hypothesis, we aimed to inhibit b
Autor:
Michalina Ignasik, Marek Bajda, Natalia Guzior, Ulrike Holzgrabe, Barbara Malawska, Michaela Prinz
Publikováno v:
Archiv der Pharmazie. 345:509-516
A new series of 2-(diethylaminoalkyl)-isoindoline-1,3-dione derivatives intended as dual binding site cholinesterase inhibitors were designed using molecular modeling and evaluated as inhibitors of acetylcholinesterase (AChE), butyrylcholinesterase (
Autor:
Michaela Prinz, Thomas Erker, Gerda Brunhofer, Przemyslaw Guzik, Adyary Fallarero, Daniela Karlsson, Pia Vuorela, Ulrike Holzgrabe
Publikováno v:
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences. 45(1-2)
In this contribution, a chemical collection of aromatic compounds was screened for inhibition on butyrylcholinesterase (BChE)’s hydrolase activity using Ellman’s reaction. A set of diarylimidazoles was identified as highly selective inhibitors of
Autor:
Adyary Fallarero, Holger Braunschweig, Josef Scheiber, Pia Vuorela, Ercin Erciyas, Vildan Alptüzün, Krzysztof Radacki, Verena Hörr, Bernd Engels, Michaela Prinz, Ulrike Holzgrabe
Publikováno v:
Bioorganicmedicinal chemistry. 18(5)
Approved drugs for the treatment of Alzheimer's disease belong to the group of inhibitors of the acetylcholinesterase (AChE) and NMDA receptor inhibitors. However none of the drugs is able to combat or reverse the progression of the disease. Thus, th