skip to main content
Idioma:
Refinado por: Nome da Publicação: Journal Of Medicinal Chemistry remover assunto: Science & Technology remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Investigations on the 1-(2-biphenyl)piperazine motif: identification of new potent and selective ligands for the serotonin(7) (5-HT(7)) receptor with agonist or antagonist action in vitro or ex vivo
Investigations on the 1-(2-biphenyl)piperazine motif: identification of new potent and selective ligands for the serotonin(7) (5-HT(7)) receptor with agonist or antagonist action in vitro or ex vivo
Material Type:
Artigo 		Adicionar ao Meu Espaço

Investigations on the 1-(2-biphenyl)piperazine motif: identification of new potent and selective ligands for the serotonin(7) (5-HT(7)) receptor with agonist or antagonist action in vitro or ex vivo

Lacivita, Enza ; Patarnello, Daniela ; Stroth, Nikolas ; Caroli, Antonia ; Niso, Mauro ; Contino, Marialessandra ; De Giorgio, Paola ; Di Pilato, Pantaleo ; Colabufo, Nicola A ; Berardi, Francesco ; Perrone, Roberto ; Svenningsson, Per ; Hedlund, Peter B ; Leopoldo, Marcello

Journal of medicinal chemistry, 2012-07, Vol.55 (14), p.6375-6380 [Periódico revisado por pares]

United States

Texto completo disponível

Citações Citado por
2
New σ and 5-HT1A Receptor Ligands:  ω-(Tetralin-1-yl)-n-alkylamine Derivatives
New σ and 5-HT1A Receptor Ligands:  ω-(Tetralin-1-yl)-n-alkylamine Derivatives
Material Type:
Artigo 		Adicionar ao Meu Espaço

New σ and 5-HT1A Receptor Ligands:  ω-(Tetralin-1-yl)-n-alkylamine Derivatives

Berardi, Francesco ; Colabufo, Nicola A ; Giudice, Giuseppe ; Perrone, Roberto ; Tortorella, Vincenzo ; Govoni, Stefano ; Lucchi, Laura

Journal of medicinal chemistry, 1996-01, Vol.39 (1), p.176-182 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
3
Structure−Affinity Relationship Study on N -[4-(4-Arylpiperazin-1-yl)butyl]arylcarboxamides as Potent and Selective Dopamine D 3 Receptor Ligands
Structure−Affinity Relationship Study on N -[4-(4-Arylpiperazin-1-yl)butyl]arylcarboxamides as Potent and Selective Dopamine D 3 Receptor Ligands
Material Type:
Artigo 		Adicionar ao Meu Espaço

Structure−Affinity Relationship Study on N -[4-(4-Arylpiperazin-1-yl)butyl]arylcarboxamides as Potent and Selective Dopamine D 3 Receptor Ligands

Leopoldo, Marcello ; Berardi, Francesco ; Colabufo, Nicola A. ; De Giorgio, Paola ; Lacivita, Enza ; Perrone, Roberto ; Tortorella, Vincenzo

Journal of medicinal chemistry, 2002-12, Vol.45 (26), p.5727-5735 [Periódico revisado por pares]

Texto completo disponível

Citações Citado por
4
First Structure−Activity Relationship Study on Dopamine D 3 Receptor Agents with N -[4-(4-Arylpiperazin-1-yl)butyl]arylcarboxamide Structure
First Structure−Activity Relationship Study on Dopamine D 3 Receptor Agents with N -[4-(4-Arylpiperazin-1-yl)butyl]arylcarboxamide Structure
Material Type:
Artigo 		Adicionar ao Meu Espaço

First Structure−Activity Relationship Study on Dopamine D 3 Receptor Agents with N -[4-(4-Arylpiperazin-1-yl)butyl]arylcarboxamide Structure

Leopoldo, Marcello ; Lacivita, Enza ; Colabufo, Nicola A. ; Contino, Marialessandra ; Berardi, Francesco ; Perrone, Roberto

Journal of medicinal chemistry, 2005-12, Vol.48 (25), p.7919-7922 [Periódico revisado por pares]

Texto completo disponível

Citações Citado por
5
Methyl substitution on the piperidine ring of N-[omega-(6-methoxynaphthalen-1-yl)alkyl] derivatives as a probe for selective binding and activity at the sigma(1) receptor
Methyl substitution on the piperidine ring of N-[omega-(6-methoxynaphthalen-1-yl)alkyl] derivatives as a probe for selective binding and activity at the sigma(1) receptor
Material Type:
Artigo 		Adicionar ao Meu Espaço

Methyl substitution on the piperidine ring of N-[omega-(6-methoxynaphthalen-1-yl)alkyl] derivatives as a probe for selective binding and activity at the sigma(1) receptor

Berardi, Francesco ; Ferorelli, Savina ; Abate, Carmen ; Pedone, Maria P ; Colabufo, Nicola A ; Contino, Marialessandra ; Perrone, Roberto

Journal of medicinal chemistry, 2005-12, Vol.48 (26), p.8237-8244 [Periódico revisado por pares]

United States

Texto completo disponível

Citações Citado por
6
Synthesis and Structure−Affinity Relationships of 1-[ω-(4-Aryl-1-piperazinyl)alkyl]-1-aryl Ketones as 5-HT7 Receptor Ligands
Synthesis and Structure−Affinity Relationships of 1-[ω-(4-Aryl-1-piperazinyl)alkyl]-1-aryl Ketones as 5-HT7 Receptor Ligands
Material Type:
Artigo 		Adicionar ao Meu Espaço

Synthesis and Structure−Affinity Relationships of 1-[ω-(4-Aryl-1-piperazinyl)alkyl]-1-aryl Ketones as 5-HT7 Receptor Ligands

Perrone, Roberto ; Berardi, Francesco ; Colabufo, Nicola A ; Lacivita, Enza ; Leopoldo, Marcello ; Tortorella, Vincenzo

Journal of medicinal chemistry, 2003-02, Vol.46 (4), p.646-649 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
7
A Structure−Affinity Relationship Study on Derivatives of N -[2-[4-(4-Chlorophenyl)piperazin-1-yl]ethyl]-3-methoxybenzamide, a High-Affinity and Selective D 4 Receptor Ligand
A Structure−Affinity Relationship Study on Derivatives of N -[2-[4-(4-Chlorophenyl)piperazin-1-yl]ethyl]-3-methoxybenzamide, a High-Affinity and Selective D 4 Receptor Ligand
Material Type:
Artigo 		Adicionar ao Meu Espaço

A Structure−Affinity Relationship Study on Derivatives of N -[2-[4-(4-Chlorophenyl)piperazin-1-yl]ethyl]-3-methoxybenzamide, a High-Affinity and Selective D 4 Receptor Ligand

Perrone, Roberto ; Berardi, Francesco ; Colabufo, Nicola A. ; Leopoldo, Marcello ; Tortorella, Vincenzo

Journal of medicinal chemistry, 2000-01, Vol.43 (2), p.270-277 [Periódico revisado por pares]

Texto completo disponível

Citações Citado por
8
N -[2-[4-(4-Chlorophenyl)piperazin-1-yl]ethyl]-3-methoxybenzamide:  A Potent and Selective Dopamine D 4 Ligand
N -[2-[4-(4-Chlorophenyl)piperazin-1-yl]ethyl]-3-methoxybenzamide:  A Potent and Selective Dopamine D 4 Ligand
Material Type:
Artigo 		Adicionar ao Meu Espaço

N -[2-[4-(4-Chlorophenyl)piperazin-1-yl]ethyl]-3-methoxybenzamide:  A Potent and Selective Dopamine D 4 Ligand

Perrone, Roberto ; Berardi, Francesco ; Colabufo, Nicola A. ; Leopoldo, Marcello ; Tortorella, Vincenzo

Journal of medicinal chemistry, 1998-11, Vol.41 (24), p.4903-4909 [Periódico revisado por pares]

Texto completo disponível

Citações Citado por
9
Structure−Activity Relationship Studies on the 5-HT1A Receptor Affinity of 1-Phenyl-4-[ω-(α- or β-tetralinyl)alkyl]piperazines. 4
Structure−Activity Relationship Studies on the 5-HT1A Receptor Affinity of 1-Phenyl-4-[ω-(α- or β-tetralinyl)alkyl]piperazines. 4
Material Type:
Artigo 		Adicionar ao Meu Espaço

Structure−Activity Relationship Studies on the 5-HT1A Receptor Affinity of 1-Phenyl-4-[ω-(α- or β-tetralinyl)alkyl]piperazines. 4

Perrone, Roberto ; Berardi, Francesco ; Colabufo, Nicola A ; Leopoldo, Marcello ; Tortorella, Vincenzo ; Fornaretto, Maria Gioia ; Caccia, Carla ; McArthur, Robert A

Journal of medicinal chemistry, 1996-12, Vol.39 (25), p.4928-4934 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
10
Mixed 5-HT1A/D-2 activity of a new model of arylpiperazines: 1-aryl-4-[3-(1,2-dihydronaphthalen-4-yl)-n-propyl]piperazines. 1. Synthesis and structure-activity relationships
Mixed 5-HT1A/D-2 activity of a new model of arylpiperazines: 1-aryl-4-[3-(1,2-dihydronaphthalen-4-yl)-n-propyl]piperazines. 1. Synthesis and structure-activity relationships
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mixed 5-HT1A/D-2 activity of a new model of arylpiperazines: 1-aryl-4-[3-(1,2-dihydronaphthalen-4-yl)-n-propyl]piperazines. 1. Synthesis and structure-activity relationships

Perrone, Roberto ; Berardi, Francesco ; Colabufo, Nicola A ; Tortorella, Vincenzo ; Fiorentini, Francesco ; Olgiati, Vincenzo ; Vanotti, Ermes ; Govoni, Stefano

Journal of medicinal chemistry, 1994-01, Vol.37 (1), p.99-104 [Periódico revisado por pares]

United States: American Chemical Society

Texto completo disponível

Citações Citado por

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.