Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/201582
Type: Artigo de periódico
Title: Synthesis And Antiproliferative Activity Of 8-hydroxyquinoline Derivatives Containing A 1,2,3-triazole Moiety.
Author: Freitas, Luiza B de O
Borgati, Thiago F
de Freitas, Rossimiriam P
Ruiz, Ana L T G
Marchetti, Gabriela M
de Carvalho, João E
da Cunha, Elaine F F
Ramalho, Teodorico C
Alves, Rosemeire B
Abstract: Twelve novel 8-hydroxyquinoline derivatives were synthesized with good yields by performing copper-catalyzed Huisgen 1,3-dipolar cycloaddition (click reaction) between an 8-O-alkylated-quinoline containing a terminal alkyne and various aromatic or protected sugar azides. These compounds were evaluated in vitro for their antiproliferative activity on various cancer cell types. Protected sugar derivative 16 was the most active compound in the series, exhibiting potent antiproliferative activity and high selectivity toward ovarian cancer cells (OVCAR-03, GI50 < 0.25 μg mL(-1)); this derivative was more active than the reference drug doxorubicin (OVCAR-03, GI50 = 0.43 μg mL(-1)). In structure-activity relationship (SAR) studies, the physico-chemical parameters of the compounds were evaluated and docking calculations were performed for the α-glucosidase active site to predict the possible mechanism of action of this series of compounds.
Subject: 1,2,3-triazole
8-hydroxyquinoline
Antiproliferative
“click” Reaction
Rights: fechado
Identifier DOI: 10.1016/j.ejmech.2014.07.061
Address: http://www.ncbi.nlm.nih.gov/pubmed/25062010
Date Issue: 2014
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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