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Substituted tetraazaacenaphthylenes as potent CRF1 receptor antagonists for the treatment of depression and anxiety
Substituted tetraazaacenaphthylenes as potent CRF1 receptor antagonists for the treatment of depression and anxiety
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Substituted tetraazaacenaphthylenes as potent CRF1 receptor antagonists for the treatment of depression and anxiety

St-Denis, Y ; Di Fabio, R ; Bernasconi, G ; Castiglioni, E ; Contini, S ; Donati, D ; Fazzolari, E ; Gentile, G ; Ghirlanda, D ; Marchionni, C ; Messina, F ; Micheli, F ; Pavone, F ; Pasquarello, A ; Sabbatini, F M ; Zampori, M G ; Arban, R ; Vitulli, G

Bioorganic & medicinal chemistry letters, 2005-08, Vol.15 (16), p.3713-3716 [Periódico revisado por pares]

England

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2
Enantiomerically pure tetrahydroquinoline derivatives as in vivo potent antagonists of the glycine binding site associated to the NMDA receptor
Enantiomerically pure tetrahydroquinoline derivatives as in vivo potent antagonists of the glycine binding site associated to the NMDA receptor
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Enantiomerically pure tetrahydroquinoline derivatives as in vivo potent antagonists of the glycine binding site associated to the NMDA receptor

DI FABIO, Romano ; TRANQUILLINI, Elvira ; DONATI, Daniele ; RATTI, Emiliangelo ; ARBAN, Roberto ; DAL FORNO, Giovanna ; REGGIANI, Angelo ; BARNABY, Robert J ; BERTANI, Barbara ; ALVARO, Giuseppe ; MICHELI, Fabrizio ; SABBATINI, Fabio ; PIZZI, Maria Domenica ; PENTASSUGLIA, Giorgio ; PASQUARELLO, Alessandra ; MESSERI, Tommaso

Bioorganic & medicinal chemistry letters, 2003-11, Vol.13 (21), p.3863-3866 [Periódico revisado por pares]

Oxford: Elsevier

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3
Substituted tetraazaacenaphthylenes as potent CRF1 receptor antagonists for the treatment of depression and anxiety: G-protein-coupled receptors in drug discovery
Substituted tetraazaacenaphthylenes as potent CRF1 receptor antagonists for the treatment of depression and anxiety: G-protein-coupled receptors in drug discovery
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Substituted tetraazaacenaphthylenes as potent CRF1 receptor antagonists for the treatment of depression and anxiety: G-protein-coupled receptors in drug discovery

ST-DENIS, Y ; DI FABIO, R ; MESSINA, F ; MICHELI, F ; PAVONE, F ; PASQUARELLO, A ; SABBATINI, F. M ; ZAMPORI, M. G ; ARBAN, R ; VITULLI, G ; BERNASCONI, G ; CASTIGLIONI, E ; CONTINI, S ; DONATI, D ; FAZZOLARI, E ; GENTILE, G ; GHIRLANDA, D ; MARCHIONNI, C

Bioorganic & medicinal chemistry letters, 2005, Vol.15 (16), p.3713-3716 [Periódico revisado por pares]

Oxford: Elsevier

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4
From pyrroles to pyrrolo[1,2- a]pyrazinones: A new class of mGluR1 antagonists
From pyrroles to pyrrolo[1,2- a]pyrazinones: A new class of mGluR1 antagonists
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From pyrroles to pyrrolo[1,2- a]pyrazinones: A new class of mGluR1 antagonists

Micheli, Fabrizio ; Cavanni, Paolo ; Di Fabio, Romano ; Marchioro, Carla ; Donati, Daniele ; Faedo, Stefania ; Maffeis, Micaela ; Sabbatini, Fabio Maria ; Tranquillini, Maria Elvira

Bioorganic & medicinal chemistry letters, 2006-03, Vol.16 (5), p.1342-1345 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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5
2,4-Dicarboxy-pyrroles as selective non-Competitive mGluR1 antagonists: further characterization of 3,5-Dimethyl pyrrole-2,4-dicarboxylic acid 2-propyl ester 4-(1,2,2-Trimethyl-propyl) ester and structure–Activity relationships
2,4-Dicarboxy-pyrroles as selective non-Competitive mGluR1 antagonists: further characterization of 3,5-Dimethyl pyrrole-2,4-dicarboxylic acid 2-propyl ester 4-(1,2,2-Trimethyl-propyl) ester and structure–Activity relationships
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2,4-Dicarboxy-pyrroles as selective non-Competitive mGluR1 antagonists: further characterization of 3,5-Dimethyl pyrrole-2,4-dicarboxylic acid 2-propyl ester 4-(1,2,2-Trimethyl-propyl) ester and structure–Activity relationships

Micheli, Fabrizio ; Di Fabio, Romano ; Bordi, Fabio ; Cavallini, Palmina ; Cavanni, Paolo ; Donati, Daniele ; Faedo, Stefania ; Maffeis, Micaela ; Sabbatini, Fabio Maria ; Tarzia, Giorgio ; Tranquillini, Maria Elvira

Bioorganic & medicinal chemistry letters, 2003-07, Vol.13 (13), p.2113-2118 [Periódico revisado por pares]

England: Elsevier Ltd

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6
Discovery and structure–activity relationship of 2-phenyl-oxazole-4-carboxamide derivatives as potent apoptosis inducers
Discovery and structure–activity relationship of 2-phenyl-oxazole-4-carboxamide derivatives as potent apoptosis inducers
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Discovery and structure–activity relationship of 2-phenyl-oxazole-4-carboxamide derivatives as potent apoptosis inducers

Tai, Vincent W.-F. ; Sperandio, David ; Shelton, Emma J. ; Litvak, Joane ; Pararajasingham, Keith ; Cebon, Ben ; Lohman, Julia ; Eksterowicz, John ; Kantak, Seema ; Sabbatini, Peter ; Brown, Cindy ; Zeitz, Jennifer ; Reed, Chris ; Maske, Bill ; Graupe, Doris ; Estevez, Alberto ; Oeh, Jason ; Wong, Darren ; Ni, Yong ; Sprengeler, Paul ; Yee, Robert ; Magill, Catherine ; Neri, Anthony ; Cai, Sui Xiong ; Drewe, John ; Qiu, Ling ; Herich, John ; Tseng, Ben ; Kasibhatla, Shailaja ; Spencer, Jeffrey R.

Bioorganic & medicinal chemistry letters, 2006-09, Vol.16 (17), p.4554-4558 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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7
Substituted tetraazaacenaphthylenes as potent CRF 1 receptor antagonists for the treatment of depression and anxiety
Substituted tetraazaacenaphthylenes as potent CRF 1 receptor antagonists for the treatment of depression and anxiety
Material Type:
Artigo 		Adicionar ao Meu Espaço

Substituted tetraazaacenaphthylenes as potent CRF 1 receptor antagonists for the treatment of depression and anxiety

St-Denis, Y. ; Fabio, R. Di ; Bernasconi, G. ; Castiglioni, E. ; Contini, S. ; Donati, D. ; Fazzolari, E. ; Gentile, G. ; Ghirlanda, D. ; Marchionni, C. ; Messina, F. ; Micheli, F. ; Pavone, F. ; Pasquarello, A. ; Sabbatini, F.M. ; Zampori, M.G. ; Arban, R. ; Vitulli, G.

Bioorganic & medicinal chemistry letters, 2005, Vol.15 (16), p.3713-3716 [Periódico revisado por pares]

Elsevier Ltd

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