Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Danai-Dionysia Fourla"'
Autor:
Maria-Pagona Papakonstantinou, Zafiroula Georgoussi, Danai-Dionysia Fourla, Stavroula-Maria Vrana
Publikováno v:
Cellular Signalling. 24:2315-2328
Previous studies have shown that the intracellular domains of opioid receptors serve as platforms for the formation of a multi-component signaling complex consisting of various interacting partners (Leontiadis et al., 2009, Cell Signal. 21, 1218–12
Autor:
Alexandra Gramowski-Voss, Zafiroula Georgoussi, Dieter G. Weiss, Dirk Tourwé, A. W. Lipkowski, Bart Vandormael, Olaf Schröder, Piotr Kosson, Danai-Dionysia Fourla
Publikováno v:
Journal of Medicinal Chemistry. 54:7848-7859
Novel dermorphin tetrapeptides are described in which Tyr1 is replaced by Dmt1, where d-Ala2 and Gly4 are N-methylated, and where Phe3-Gly4 residue is substituted by the constrained Aba3-Gly4 peptidomimetic. Most of these peptidic ligands displayed b
Autor:
Rita Turnaturi, Agostino Marrazzo, Danai-Dionysia Fourla, Zafiroula Georgoussi, Giovanna M. Scoto, Orazio Prezzavento, Carmela Parenti, Giuseppina Aricò, Simone Ronsisvalle, Lorella Pasquinucci, Giuseppe Ronsisvalle
Aims Powerful analgesics relieve pain primarily through activating mu opioid receptor (MOR), but the long-term use of MOR agonists, such as morphine, is limited by the rapid development of tolerance. Recently, it has been observed that simultaneous s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8f8442963e2f751316ded99efb2062e
http://hdl.handle.net/20.500.11769/41140
http://hdl.handle.net/20.500.11769/41140
Autor:
Bart, Vandormael, Danai-Dionysia, Fourla, Alexandra, Gramowski-Voss, Piotr, Kosson, Dieter G, Weiss, Olaf H-U, Schröder, Andrzej, Lipkowski, Zafiroula, Georgoussi, Dirk, Tourwé
Publikováno v:
Journal of medicinal chemistry. 54(22)
Novel dermorphin tetrapeptides are described in which Tyr(1) is replaced by Dmt(1), where d-Ala(2) and Gly(4) are N-methylated, and where Phe(3)-Gly(4) residue is substituted by the constrained Aba(3)-Gly(4) peptidomimetic. Most of these peptidic lig
The benzomorphan-based LP1 ligand is a suitable MOP/DOP receptors agonist for chronic pain treatment
Autor:
Pasquinucci, Lorella Giuseppina, Rita, Turnaturi, Parenti, Carmela, Giuseppina, Aricò, GIOVANNA MARIA SCOTO, Zafiroula, Georgoussi, DANAI DIONYSIA FOURLA AND GIUSEPPE RONSISVALLE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4731::a812fe214f048946756c5050d2434f6b
http://hdl.handle.net/20.500.11769/110247
http://hdl.handle.net/20.500.11769/110247
Autor:
Zafiroula Georgoussi, Lorella Pasquinucci, Giuseppina Aricò, Danai-Dionysia Fourla, Giuseppe Ronsisvalle, Emanuele Amata, Orazio Prezzavento, Agostino Marrazzo, Simone Ronsisvalle, Giovanna M. Scoto, Carmela Parenti
6,7-benzomorphan derivatives, exhibiting different mu, delta, and kappa receptor selectivity profiles depending on the N-substituent, represent a useful skeleton for the synthesis of new and better analgesic agents. In this work, an aromatic ring and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85c135923e445f34b26bcc9dcf2a7aec
http://hdl.handle.net/20.500.11769/8221
http://hdl.handle.net/20.500.11769/8221
Autor:
Bart Vandormael, Danai-Dionysia Fourla, Alexandra Gramowski-VoÃ, Piotr Kosson, Dieter G. Weiss, Olaf H.-U. SchroÌder, Andrzej Lipkowski, Zafiroula Georgoussi, Dirk TourweÌ
Publikováno v:
Journal of Medicinal Chemistry; Nov2011, Vol. 54 Issue 22, p7848-7859, 12p