Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Giovanna Dal Forno"'
Autor:
Ilaria Sartori, Laura Zonzini, Laurie J. Gordon, Angela Worby, Stefano Fontana, Manuela Borriello, Silvia Bison, Jeannette M. Watson, Steven Mark Bromidge, Giovanna Dal Forno, Colin Philip Leslie, Alessandra Pasquarello, Anna Sava, Luca G. Moccia, Barbara Bertani, Roberto Arban, Daniele Donati, Enrica Granci, Valeria Zucchelli, Paolo Cavanni, Massimo Gianotti, Romano Di-Fabio
Publikováno v:
Journal of Medicinal Chemistry. 53:5827-5843
Bioisoteric replacement of the metabolically labile N-methyl amide group of a series of benzoxazinones with small heterocyclic rings has led to novel series of fused tricyclic benzoxazines which are potent 5-HT1A/B/D receptor antagonists with and wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2fb74da943dfb46e7a247dd0b3079e2
https://doi.org/10.1021/jm100482n
https://doi.org/10.1021/jm100482n
Autor:
Claudia Mundi, Sebastien Guery, Alberto Buson, Romano Di Fabio, Sergio Melotto, Federico Faggioni, Chiara Savoia, Michela Tessari, Lucilla D'Adamo, Fabio Maria Sabbatini, Carla Di Francesco, Benedetta Perini, Paolo Cavanni, Giovanna Dal Forno, Steve M. Bromidge, Yves St-Denis, Stefania Contini, Mauro Corsi, Elisabetta Perdona, Francesca Pavone, Marilisa Rinaldi, Carpenter Andrew J, Mario Mattioli
Publikováno v:
ChemMedChem. 5:1450-1455
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36057954bce91c40c062ae6ddd7a994f
https://doi.org/10.1002/cmdc.201000185
https://doi.org/10.1002/cmdc.201000185
Autor:
Steven M, Bromidge, Roberto, Arban, Barbara, Bertani, Silvia, Bison, Manuela, Borriello, Paolo, Cavanni, Giovanna, Dal Forno, Romano, Di-Fabio, Daniele, Donati, Stefano, Fontana, Massimo, Gianotti, Laurie J, Gordon, Enrica, Granci, Colin P, Leslie, Luca, Moccia, Alessandra, Pasquarello, Ilaria, Sartori, Anna, Sava, Jeannette M, Watson, Angela, Worby, Laura, Zonzini, Valeria, Zucchelli
Publikováno v:
Journal of medicinal chemistry. 53(15)
Bioisoteric replacement of the metabolically labile N-methyl amide group of a series of benzoxazinones with small heterocyclic rings has led to novel series of fused tricyclic benzoxazines which are potent 5-HT(1A/B/D) receptor antagonists with and w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::db3e73771267ce95dfc8d88c85ab0a7e
https://pubmed.ncbi.nlm.nih.gov/20590088
https://pubmed.ncbi.nlm.nih.gov/20590088
Autor:
Giorgio Pentassuglia, Romano Di Fabio, Fabio Maria Sabbatini, Barbara Bertani, Maria Domenica Pizzi, Emiliangelo Ratti, Angelo Reggiani, Alessandra Pasquarello, Daniele Donati, Robert J. Barnaby, Giovanna Dal Forno, Roberto Arban, Elvira Tranquillini, Tommaso Messeri, Giuseppe Alvaro, Fabrizio Micheli
Publikováno v:
Bioorganicmedicinal chemistry letters. 13(21)
To identify neuroprotective agents after stroke, new substituted tetrahydroquinoline derivatives were designed as antagonists of the glycine binding site associated to the NMDA receptor, satisfying the key pharmacophoric requirements. In particular,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cd92fe6ccf740b80d803007cbccf174
https://pubmed.ncbi.nlm.nih.gov/14552796
https://pubmed.ncbi.nlm.nih.gov/14552796
Publikováno v:
European journal of pharmacology. 391(3)
Binding of the glycine site antagonist 3-[2-(Phenylamino-carbonyl)ethenyl]-4,6-dichloro-indole-2-carboxylic acid sodium salt ([ 3 H]GV150526A) was characterised in rat cerebral cortical membranes. Saturation experiments indicated the existence of a h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::325a5230b9b712d384465a3f86df0106
https://pubmed.ncbi.nlm.nih.gov/10729363
https://pubmed.ncbi.nlm.nih.gov/10729363
Publikováno v:
Pharmacological Research. 26:81
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11f36eab654b7f357973c50582d1af8b
https://doi.org/10.1016/1043-6618(92)90872-9
https://doi.org/10.1016/1043-6618(92)90872-9