SYNTHESIS AND LEISHMANICIDAL ACTIVITY OF NEW BIS-ALKYLQUINOLINES
Bis-alkylquinolines 1-6 were synthetized via Williamson reaction between 8-hydroxyquinaldine with different É, ù-dihaloalkanes. Structures of all the products were elucidated by spectroscopic analysis. Cytotoxic and antileishmanial activities of synthesized compounds were determinated on U-937 cells...
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Sociedad Chilena de Química
2013
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oai:scielo:S0717-970720130002000142014-09-09SYNTHESIS AND LEISHMANICIDAL ACTIVITY OF NEW BIS-ALKYLQUINOLINESCARDONA,WILSONARANGO,VICTORDOMÍNGUEZ,JORGE JROBLEDO,SARA MMUÑOZ,DIANA LFIGADERE,BRUNOVELEZ,IVAN DSÁEZ,JAIRO Leishmania antiprotozoal quinoline Bis-alkylquinolines 1-6 were synthetized via Williamson reaction between 8-hydroxyquinaldine with different É, ù-dihaloalkanes. Structures of all the products were elucidated by spectroscopic analysis. Cytotoxic and antileishmanial activities of synthesized compounds were determinated on U-937 cells and L. (V) panamensis amastigotes, respectively. Compound 5, 1,9-bis[(2-methylquinolin-8-yl)oxy]nonane, was the most selective against axenic and intracellular amastigotes (EC50 = 11.3 and 22.6, ìg/mL), with selectivity indices greater than 17.7 and 8.8, respectively; which makes this compound promising for the developing of new leishmanicidal drugs.info:eu-repo/semantics/openAccessSociedad Chilena de QuímicaJournal of the Chilean Chemical Society v.58 n.2 20132013-01-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072013000200014en10.4067/S0717-97072013000200014 |
institution |
Scielo Chile |
collection |
Scielo Chile |
language |
English |
topic |
Leishmania antiprotozoal quinoline |
spellingShingle |
Leishmania antiprotozoal quinoline CARDONA,WILSON ARANGO,VICTOR DOMÍNGUEZ,JORGE J ROBLEDO,SARA M MUÑOZ,DIANA L FIGADERE,BRUNO VELEZ,IVAN D SÁEZ,JAIRO SYNTHESIS AND LEISHMANICIDAL ACTIVITY OF NEW BIS-ALKYLQUINOLINES |
description |
Bis-alkylquinolines 1-6 were synthetized via Williamson reaction between 8-hydroxyquinaldine with different É, ù-dihaloalkanes. Structures of all the products were elucidated by spectroscopic analysis. Cytotoxic and antileishmanial activities of synthesized compounds were determinated on U-937 cells and L. (V) panamensis amastigotes, respectively. Compound 5, 1,9-bis[(2-methylquinolin-8-yl)oxy]nonane, was the most selective against axenic and intracellular amastigotes (EC50 = 11.3 and 22.6, ìg/mL), with selectivity indices greater than 17.7 and 8.8, respectively; which makes this compound promising for the developing of new leishmanicidal drugs. |
author |
CARDONA,WILSON ARANGO,VICTOR DOMÍNGUEZ,JORGE J ROBLEDO,SARA M MUÑOZ,DIANA L FIGADERE,BRUNO VELEZ,IVAN D SÁEZ,JAIRO |
author_facet |
CARDONA,WILSON ARANGO,VICTOR DOMÍNGUEZ,JORGE J ROBLEDO,SARA M MUÑOZ,DIANA L FIGADERE,BRUNO VELEZ,IVAN D SÁEZ,JAIRO |
author_sort |
CARDONA,WILSON |
title |
SYNTHESIS AND LEISHMANICIDAL ACTIVITY OF NEW BIS-ALKYLQUINOLINES |
title_short |
SYNTHESIS AND LEISHMANICIDAL ACTIVITY OF NEW BIS-ALKYLQUINOLINES |
title_full |
SYNTHESIS AND LEISHMANICIDAL ACTIVITY OF NEW BIS-ALKYLQUINOLINES |
title_fullStr |
SYNTHESIS AND LEISHMANICIDAL ACTIVITY OF NEW BIS-ALKYLQUINOLINES |
title_full_unstemmed |
SYNTHESIS AND LEISHMANICIDAL ACTIVITY OF NEW BIS-ALKYLQUINOLINES |
title_sort |
synthesis and leishmanicidal activity of new bis-alkylquinolines |
publisher |
Sociedad Chilena de Química |
publishDate |
2013 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072013000200014 |
work_keys_str_mv |
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1718445486817411072 |