Design and synthesis of a new coumarin-based 'turn-on' fluorescent probe selective for Cu+2
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
04/11/2013
04/11/2013
2012
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Resumo |
The novel coumarin-based 'turn-on' fluorescent probe (E)-3-(2,5-dimethoxybenzylideneamino)-7-hydroxy-2H-chromen-2-one (MGM) was designed, synthesized, and characterized. This compound shows high selectivity for Cu+2, combined with a large fluorescence enhancement upon binding to Cu2+. Benesi-Hildebrand and Job plots demonstrate that the stoichiometry of the Cu+2 complex formed is 2:1. Preliminary studies employing epifluorescence microscopy demonstrated that Cu+2 could be imaged in human neuroblastoma SH-SY5Y cells treated with MGM. (c) 2012 Elsevier Ltd. All rights reserved. Millennium Scientific Initiative Millennium Scientific Initiative [P05-001-F] Institut Nacional de Ciencia e Tecnologia do Meio Ambiente-USP (Brazil) Institut Nacional de Ciencia e Tecnologia do Meio AmbienteUSP (Brazil) Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) CNPq (Brazil) CNPq-Brazil |
Identificador |
TETRAHEDRON LETTERS, OXFORD, v. 53, n. 39, p. 5280-5283, SEP 26, 2012 0040-4039 http://www.producao.usp.br/handle/BDPI/37804 10.1016/j.tetlet.2012.07.082 |
Idioma(s) |
eng |
Publicador |
PERGAMON-ELSEVIER SCIENCE LTD OXFORD |
Relação |
TETRAHEDRON LETTERS |
Direitos |
closedAccess Copyright PERGAMON-ELSEVIER SCIENCE LTD |
Palavras-Chave | #CU+2 ION #TURN-ON PROBES #COUMARIN SCHIFF BASE #FLUORESCENCE SENSOR #COPPER #DISEASE #CU2+ #CHEMOSENSOR #ATPASE #GENE #CHEMISTRY, ORGANIC |
Tipo |
article original article publishedVersion |