Biological evaluation of novel 6-Arylbenzimidazo [1,2-c] quinazoline derivatives as inhibitors of LPS-induced TNF- alpha secretion
This study describes the effect of novel 6-Arylbenzimidazo [1,2-c] quinazoline derivatives as tumor necrosis factor alpha (TNF-á) production inhibitors. The newly synthesized compounds were tested for their in vitro ability to inhibit the lipolysaccharide (LPS) induced TNF-á secretion in the human p...
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Sociedad de Biología de Chile
2008
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Acceso en línea: | http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602008000100006 |
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oai:scielo:S0716-976020080001000062008-08-21Biological evaluation of novel 6-Arylbenzimidazo [1,2-c] quinazoline derivatives as inhibitors of LPS-induced TNF- alpha secretionGALARCE,GLORIA DFONCEA,ROCÍO EEDWARDS,ANA MPESSOA-MAHANA,HERNÁNPESSOA-MAHANA,CARLOS DEBENSPERGER,ROBERTO A anti-inflammatory agents benzimidazoquinazoline derivatives TNF-á inhibitors This study describes the effect of novel 6-Arylbenzimidazo [1,2-c] quinazoline derivatives as tumor necrosis factor alpha (TNF-á) production inhibitors. The newly synthesized compounds were tested for their in vitro ability to inhibit the lipolysaccharide (LPS) induced TNF-á secretion in the human promyelocytic cell line HL-60. The compound 6-Phenyl-benzimidazo [1,2-c] quinazoline, coded as Gl, resulted as the most potent inhibitor and with no significant cytotoxic activity. Thus, 6-Arylbenzimidazo [1,2-c] quinazoline derivatives may have a potential as anti-inflammatory agentsinfo:eu-repo/semantics/openAccessSociedad de Biología de ChileBiological Research v.41 n.1 20082008-01-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602008000100006en10.4067/S0716-97602008000100006 |
institution |
Scielo Chile |
collection |
Scielo Chile |
language |
English |
topic |
anti-inflammatory agents benzimidazoquinazoline derivatives TNF-á inhibitors |
spellingShingle |
anti-inflammatory agents benzimidazoquinazoline derivatives TNF-á inhibitors GALARCE,GLORIA D FONCEA,ROCÍO E EDWARDS,ANA M PESSOA-MAHANA,HERNÁN PESSOA-MAHANA,CARLOS D EBENSPERGER,ROBERTO A Biological evaluation of novel 6-Arylbenzimidazo [1,2-c] quinazoline derivatives as inhibitors of LPS-induced TNF- alpha secretion |
description |
This study describes the effect of novel 6-Arylbenzimidazo [1,2-c] quinazoline derivatives as tumor necrosis factor alpha (TNF-á) production inhibitors. The newly synthesized compounds were tested for their in vitro ability to inhibit the lipolysaccharide (LPS) induced TNF-á secretion in the human promyelocytic cell line HL-60. The compound 6-Phenyl-benzimidazo [1,2-c] quinazoline, coded as Gl, resulted as the most potent inhibitor and with no significant cytotoxic activity. Thus, 6-Arylbenzimidazo [1,2-c] quinazoline derivatives may have a potential as anti-inflammatory agents |
author |
GALARCE,GLORIA D FONCEA,ROCÍO E EDWARDS,ANA M PESSOA-MAHANA,HERNÁN PESSOA-MAHANA,CARLOS D EBENSPERGER,ROBERTO A |
author_facet |
GALARCE,GLORIA D FONCEA,ROCÍO E EDWARDS,ANA M PESSOA-MAHANA,HERNÁN PESSOA-MAHANA,CARLOS D EBENSPERGER,ROBERTO A |
author_sort |
GALARCE,GLORIA D |
title |
Biological evaluation of novel 6-Arylbenzimidazo [1,2-c] quinazoline derivatives as inhibitors of LPS-induced TNF- alpha secretion |
title_short |
Biological evaluation of novel 6-Arylbenzimidazo [1,2-c] quinazoline derivatives as inhibitors of LPS-induced TNF- alpha secretion |
title_full |
Biological evaluation of novel 6-Arylbenzimidazo [1,2-c] quinazoline derivatives as inhibitors of LPS-induced TNF- alpha secretion |
title_fullStr |
Biological evaluation of novel 6-Arylbenzimidazo [1,2-c] quinazoline derivatives as inhibitors of LPS-induced TNF- alpha secretion |
title_full_unstemmed |
Biological evaluation of novel 6-Arylbenzimidazo [1,2-c] quinazoline derivatives as inhibitors of LPS-induced TNF- alpha secretion |
title_sort |
biological evaluation of novel 6-arylbenzimidazo [1,2-c] quinazoline derivatives as inhibitors of lps-induced tnf- alpha secretion |
publisher |
Sociedad de Biología de Chile |
publishDate |
2008 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602008000100006 |
work_keys_str_mv |
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