Synthesis of 1-naphtylpiperazine derivatives as serotoninergic ligands and their evaluation as antiproliferative agents

被引:10
|
作者
Fiorino, Ferdinando [1 ]
Magli, Elisa [1 ]
Perissutti, Elisa [1 ]
Severino, Beatrice [1 ]
Frecentese, Francesco [1 ]
Esposito, Antonella [1 ]
De Angelis, Francesca [1 ]
Incisivo, Giuseppina Maria [1 ]
Massarelli, Paola [2 ]
Nencini, Cristina [2 ]
Di Gennaro, Elena [3 ]
Budillon, Alfredo [3 ]
Di Cintio, Alessandra [3 ]
Santagada, Vincenzo [1 ]
Caliendo, Giuseppe [1 ]
机构
[1] Univ Naples Federico 2, Dipartimento Chim Farmaceut & Tossicol, I-80131 Naples, Italy
[2] Univ Siena, Dipartimento Sci Neurol Neurochirurg & Comportame, I-53100 Siena, Italy
[3] Ist Nazl Tumori Fdn G Pascale, Unita Farmacol Sperimentale, I-80131 Naples, Italy
关键词
Naphtylpiperazine; 5-HT(1A) ligands; Antiproliferative agents; PC3; cells; VITRO PHARMACOLOGICAL EVALUATION; 5-HT1A RECEPTOR LIGANDS; PROTEIN-COUPLED RECEPTORS; NORBORNENE NUCLEUS; BINDING; BRAIN; 5-HYDROXYTRYPTAMINE(1A); PROLIFERATION; INHIBITION; APOPTOSIS;
D O I
10.1016/j.ejmech.2011.03.001
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Serotonin (5-hydroxytryptamine, 5-HT) is one of the most important neuromediator involved in numerous physiological and pathophysiological processes. In addition it is well established that 5-HT acts as a growth factor on several types of non-tumoral and tumoral cells, and recently it was also related to oncogenes. 5-HT(1A) receptor expression was identified in prostatic tumor cell lines (PD cells) and in human hormone refractory prostate cancer tissue. Based on these observations, development of 5-HT(1A) antagonists could be useful in inhibiting the growth of cancer cells. In order to investigate on potential use of 5-HT(1A) ligands as antiproliferative agents, we have analyzed a new set of 1-naphtylpiperazine derivatives. In binding studies, several molecules showed affinity in nanomolar and subnanomolar range at 5-HT(1A) and moderate to no affinity for other relevant receptors (5-HT(2A), 5-HT(2C), D(1), D(2), alpha(1) and alpha(2)). All compounds were then evaluated in order to assess their antiproliferative activity using PC3 cells and the most active compounds (1 and 2) were fully characterized to define the mechanism responsible for the observed antiproliferative effect. (C) 2011 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:2206 / 2216
页数:11
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