Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Andrea Behrenswerth"'
Autor:
Christa E. Müller, Andrea Behrenswerth, Katarzyna Kieć-Kononowicz, Meryem Köse, Sabrina Gollos, Fabian Heisig, Vigneshwaran Namasivayam, Tadeusz Karcz, Amelie Fiene
Publikováno v:
Journal of Medicinal Chemistry. 61:4301-4316
Fluorescent ligands represent powerful tools for biological studies and are considered attractive alternatives to radioligands. In this study, we developed fluorescent antagonists for A2B adenosine receptors (A2BARs), which are targeted by antiasthma
Autor:
Meryem, Köse, Sabrina, Gollos, Tadeusz, Karcz, Amelie, Fiene, Fabian, Heisig, Andrea, Behrenswerth, Katarzyna, Kieć-Kononowicz, Vigneshwaran, Namasivayam, Christa E, Müller
Publikováno v:
Journal of medicinal chemistry. 61(10)
Fluorescent ligands represent powerful tools for biological studies and are considered attractive alternatives to radioligands. In this study, we developed fluorescent antagonists for A
Autor:
Andrea Behrenswerth, Karen Nieber, Christa E. Müller, Ali El-Tayeb, Sebastian Michael, Sabrina Gollos, Aliaa Abdelrahman
Publikováno v:
ACS Medicinal Chemistry Letters. 2:890-895
Adenosine A2A receptor agonists for the local treatment of inflammatory bowel disease (IBS) were designed and synthesized. Polar groups were introduced to prevent peroral absorption and subsequent systemic, e.g., hypotensive, side effects. 4-(2-{6-Am
Autor:
Schrader J, Michael Romio, Christa E. Müller, Jamshed Iqbal, Herbert Zimmermann, Andrea Behrenswerth, Ali El-Tayeb, Marion Schneider
Publikováno v:
Journal of Medicinal Chemistry. 52:7669-7677
Prodrugs of adenosine A2A receptor agonists were developed that are activated by ecto-5′-nucleotidase (ecto-5′-NT, CD73). Because ecto-5′-NT is upregulated in inflamed tissue, the A2A agonists are expected to be released from their prodrug form
Publikováno v:
Bioorganic & Medicinal Chemistry. 17:2842-2851
In the present study we synthesized 36 coumarin and 2H-chromene derivatives applying a recently developed umpoled domino reaction using substituted salicylaldehyde and alpha,beta-unsaturated aldehyde derivatives as starting compounds. In radioligand
Autor:
Tadeusz Karcz, Sonja Hinz, Maria Kaleta, Andrea Behrenswerth, K. Atzler, Dominik Thimm, Viktor Rempel, Clara T. Schoeder, Katarzyna Kieć-Kononowicz, Christa E. Müller
GPR18 and GPR55 are orphan G protein-coupled receptors (GPCRs) that interact with certain cannabinoid (CB) receptor ligands. In the present study bicyclic imidazole-4-one derivatives were discovered as new scaffolds for the development of antagonists
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33b29106adbe9fb132d21f3d84d3e75b
https://ruj.uj.edu.pl/xmlui/handle/item/106890
https://ruj.uj.edu.pl/xmlui/handle/item/106890
Autor:
Ali, El-Tayeb, Jamshed, Iqbal, Andrea, Behrenswerth, Michael, Romio, Marion, Schneider, Herbert, Zimmermann, Jürgen, Schrader, Christa E, Müller
Publikováno v:
Journal of medicinal chemistry. 52(23)
Prodrugs of adenosine A(2A) receptor agonists were developed that are activated by ecto-5'-nucleotidase (ecto-5'-NT, CD73). Because ecto-5'-NT is upregulated in inflamed tissue, the A(2A) agonists are expected to be released from their prodrug form a
Autor:
Ali El-Tayeb, Jamshed Iqbal, Andrea Behrenswerth, Michael Romio, Marion Schneider, Herbert Zimmermann, Jürgen Schrader, Christa E. Müller
Publikováno v:
Journal of Medicinal Chemistry; Dec2009, Vol. 52 Issue 23, p7669-7677, 9p