Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Carina Höring"'
Autor:
Carina Höring, Marcus Conrad, Christian A. Söldner, Jinan Wang, Heinrich Sticht, Andrea Strasser, Yinglong Miao
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 18, p 10047 (2021)
G protein-coupled receptors (GPCRs) are targets of extracellular stimuli and hence occupy a key position in drug discovery. By specific and not yet fully elucidated coupling profiles with α subunits of distinct G protein families, they regulate cell
Externí odkaz:
https://doaj.org/article/3fd1b6a9f3614a8d849c8510ffe9c43e
Autor:
Carina Höring, Ulla Seibel, Katharina Tropmann, Lukas Grätz, Denise Mönnich, Sebastian Pitzl, Günther Bernhardt, Steffen Pockes, Andrea Strasser
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 22, p 8440 (2020)
In drug discovery, assays with proximal readout are of great importance to study target-specific effects of potential drug candidates. In the field of G protein-coupled receptors (GPCRs), the determination of GPCR-G protein interactions and G protein
Externí odkaz:
https://doaj.org/article/b106ab011dc5460da9eb1dce75d2e44c
Autor:
Ulrich Gergs, Carina Höring, Charlotte Fehse, Steffen Pockes, Maren Luise Büxel, Rebecca Schwarz, Uwe Kirchhefer, Margaréta Marušáková, Joachim Neumann, Britt Hofmann, Merlin Bresinsky, Aneta Čináková
Publikováno v:
Journal of Pharmacology and Experimental Therapeutics. 379:223-234
In an integrative approach, we studied cardiac effects of recently published novel H2 receptor agonists in the heart of mice that overexpress the human H2 receptor (H2-TG mice) and littermate wild type (WT) control mice and in isolated electrically d
Publikováno v:
Journal of Medicinal Chemistry. 63:13090-13102
Currently employed histamine H2 receptor (H2R) radioligands possess several drawbacks, for example, high non-specificity, insurmountable binding, or short half-life. We report the synthesis and the chemical and pharmacological characterization of the
Publikováno v:
Journal of medicinal chemistry. 63(21)
Currently employed histamine H
Autor:
Corinna G, Weinhart, David, Wifling, Maximilian F, Schmidt, Eduard, Neu, Carina, Höring, Timothy, Clark, Peter, Gmeiner, Max, Keller
Publikováno v:
European journal of medicinal chemistry. 213
The family of human muscarinic acetylcholine receptors (MRs) is characterized by a high sequence homology among the five subtypes (M
Autor:
Katarzyna, Szczepańska, Steffen, Pockes, Sabina, Podlewska, Carina, Höring, Kamil, Mika, Gniewomir, Latacz, Marek, Bednarski, Agata, Siwek, Tadeusz, Karcz, Martin, Nagl, Merlin, Bresinsky, Denise, Mönnich, Ulla, Seibel, Kamil J, Kuder, Magdalena, Kotańska, Holger, Stark, Sigurd, Elz, Katarzyna, Kieć-Kononowicz
Publikováno v:
European journal of medicinal chemistry. 213
A series of 4-pyridylpiperazine derivatives with varying regulatory region substituents proved to be potent histamine H
Autor:
Maximilian F. Schmidt, Corinna. G. Weinhart, Eduard Neu, David Wifling, Timothy Clark, Carina Höring, Max Keller, Peter Gmeiner
Publikováno v:
European Journal of Medicinal Chemistry. 213:113159
The family of human muscarinic acetylcholine receptors (MRs) is characterized by a high sequence homology among the five subtypes (M1R-M5R), being the reason for a lack of subtype selective MR ligands. In continuation of our work on dualsteric dibenz
Autor:
Agata Siwek, Katarzyna Szczepańska, Magdalena Kotańska, Marek Bednarski, Katarzyna Kieć-Kononowicz, Martin Nagl, Holger Stark, Tadeusz Karcz, Gniewomir Latacz, Steffen Pockes, Ulla Seibel, Merlin Bresinsky, Carina Höring, Kamil Kuder, Sabina Podlewska, Denise Mönnich, Sigurd Elz, Kamil Mika
Publikováno v:
European Journal of Medicinal Chemistry. 213:113041
A series of 4-pyridylpiperazine derivatives with varying regulatory region substituents proved to be potent histamine H3 receptor (H3R) ligands in the nanomolar concentration range. The most influential modification that affected the affinity toward