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Synthesis, docking and pharmacological evaluation of novel homo- and hetero-bis 3-piperazinylpropylindole derivatives at SERT and 5-HT1A receptor

Pessoa-Mahana H.; González-Lira C.; Fierro A.; Zapata-Torres G.; Pessoa-Mahana C.D.; Ortiz-Severin J.; Iturriaga-Vásquez P.; Reyes-Parada M.; Silva-Matus P.; Saitz-Barría C.; Araya-Maturana R. (2013)

Synthesis, 5-hydroxytryptamine1A receptor affinity and docking studies of 3-[3-(4-aryl-1-piperazinyl)-propyl]-1H-indole derivatives

Pessoa-Mahana H.; Núñez C.U.; Araya-Maturana R.; Barría C.S.; Zapata-Torres G.; Pessoa-Mahana C.D.; Iturriaga-Vasquez P.; Mella-Raipán J.; Reyes-Parada M.; Celis-Barros C. (Pharmaceutical Society of Japan, 2012)

Synthesis, 5-hydroxytryptamine(1a) receptor affinity and docking studies of 3-[3-(4-aryl-1-piperazinyl)-propyl]-1h-indole derivatives

Autor desconocido (PHARMACEUTICAL SOCIETY OF JAPAN, 2012)

Synthesis, 5-hydroxytryptamine(1a) receptor affinity and docking studies of 3-[3-(4-aryl-1-piperazinyl)-propyl]-1h-indole derivatives

Autor desconocido (PHARMACEUTICAL SOCIETY OF JAPAN, 2012)

Design, synthesis and biological evaluation of 3-[4-(7-chloro-quinolin-4-yl)-piperazin-1-yl]-propionic acid hydrazones as antiprotozoal agents.

Inam, Afreen; Siddiqui, Shadab Miyan; Macedo, Taís Soares; Moreira, Diogo Rodrigo Magalhães; Leite, Ana Cristina Lima; Soares, Milena Botelho Pereira; Azam, Amir (Elsevier Masson SAS, 2014)

A Synthetic Approach Towards Novel Series Of 3-(3-(1-Piperazinyl)Propyl -1H-INDOLE Derivatives As Monoaminergic Multi-Target Agents. Docking Studies And Pharmacological Evaluation At Sert, D2, And Mao-A Receptors.

Universidad De Chile (2017)

A SYNTHETIC APPROACH TOWARDS NOVEL SERIES OF 3-(3-(1-PIPERAZINYL)PROPYL -1H-INDOLE DERIVATIVES AS MONOAMINERGIC MULTI-TARGET AGENTS. DOCKING STUDIES AND PHARMACOLOGICAL EVALUATION AT SERT, D2, AND MAO-A RECEPTORS.

Universidad de Chile (2013)

DESIGN, SYNTHESIS AND PHARMACOLOGICAL EVALUATION OF NEW SUBSTITUTED 3-[1-OXO-(4-ARYL-1-PIPERAZINYL)ALKYL]-N-(ARYLSULFONYL)-INDOLE AND INDAZOLE DERIVATIVES AS POTENTIAL DUAL ANTAGONISTS AGENTS ON 5-HT1A/5-HT6 RECEPTORS.

Pontificia Universidad Católica de Chile (2012)

Design, Synthesis And Pharmacological Evaluation Of New Substituted 3-[1-Oxo-(4-Aryl-1-Piperazinyl)Alkyl]-N-(Arylsulfonyl)-Indole And Indazole Derivatives As Potential Dual Antagonists Agents On 5-Ht1a/5-Ht6 Receptors.

Autor desconocido (2012)

Design, Synthesis And Pharmacological Evaluation Of New Substituted 3-[1-Oxo-(4-Aryl-1-Piperazinyl)Alkyl]-N-(Arylsulfonyl)-Indole And Indazole Derivatives As Potential Dual Antagonists Agents On 5-Ht1a/5-Ht6 Receptors.

Recabarren-Gajardo, Gonzalo (2017)

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Filtros

Synthesis, docking and pharmacological evaluation of novel homo- and hetero-bis 3-piperazinylpropylindole derivatives at SERT and 5-HT1A receptor

Synthesis, 5-hydroxytryptamine1A receptor affinity and docking studies of 3-[3-(4-aryl-1-piperazinyl)-propyl]-1H-indole derivatives

Synthesis, 5-hydroxytryptamine(1a) receptor affinity and docking studies of 3-[3-(4-aryl-1-piperazinyl)-propyl]-1h-indole derivatives

Synthesis, 5-hydroxytryptamine(1a) receptor affinity and docking studies of 3-[3-(4-aryl-1-piperazinyl)-propyl]-1h-indole derivatives

Design, synthesis and biological evaluation of 3-[4-(7-chloro-quinolin-4-yl)-piperazin-1-yl]-propionic acid hydrazones as antiprotozoal agents.

A Synthetic Approach Towards Novel Series Of 3-(3-(1-Piperazinyl)Propyl -1H-INDOLE Derivatives As Monoaminergic Multi-Target Agents. Docking Studies And Pharmacological Evaluation At Sert, D2, And Mao-A Receptors.

A SYNTHETIC APPROACH TOWARDS NOVEL SERIES OF 3-(3-(1-PIPERAZINYL)PROPYL -1H-INDOLE DERIVATIVES AS MONOAMINERGIC MULTI-TARGET AGENTS. DOCKING STUDIES AND PHARMACOLOGICAL EVALUATION AT SERT, D2, AND MAO-A RECEPTORS.

DESIGN, SYNTHESIS AND PHARMACOLOGICAL EVALUATION OF NEW SUBSTITUTED 3-[1-OXO-(4-ARYL-1-PIPERAZINYL)ALKYL]-N-(ARYLSULFONYL)-INDOLE AND INDAZOLE DERIVATIVES AS POTENTIAL DUAL ANTAGONISTS AGENTS ON 5-HT1A/5-HT6 RECEPTORS.

Design, Synthesis And Pharmacological Evaluation Of New Substituted 3-[1-Oxo-(4-Aryl-1-Piperazinyl)Alkyl]-N-(Arylsulfonyl)-Indole And Indazole Derivatives As Potential Dual Antagonists Agents On 5-Ht1a/5-Ht6 Receptors.

Design, Synthesis And Pharmacological Evaluation Of New Substituted 3-[1-Oxo-(4-Aryl-1-Piperazinyl)Alkyl]-N-(Arylsulfonyl)-Indole And Indazole Derivatives As Potential Dual Antagonists Agents On 5-Ht1a/5-Ht6 Receptors.