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Article in English | MEDLINE | ID: mdl-25238183

ABSTRACT

A new compound, N-(4-(1,5-diphenyl-4,5-dihydro-1H-pyrazol-3-yl)phenyl)-acrylamide (probe L), was designed and synthesized as a highly sensitive and selective fluorescent probe for recognizing and detecting thiol from other amino acids. On being mixed with thiol in buffered DMSO:HEPES=1:1 solution at pH 7.4, the probe exhibited the blue emission at 474 nm. This probe is very sensitive and displayed a linear fluorescence off-on response to thiol. The fluorescence emission of the probe is pH independent in the physiological pH range. Living cell imaging of HeLa cells confirmed its cell permeability and its ability to selectively detect thiol in cells. The structure of the probe was characterized by IR, NMR and HRMS spectroscopy analysis.


Subject(s)
Fluorescent Dyes/chemistry , Molecular Biology/methods , Sulfhydryl Compounds/analysis , Acrylamides/chemistry , Aniline Compounds/chemistry , Buffers , Chemistry Techniques, Synthetic , Cysteine/chemistry , Dimethyl Sulfoxide/chemistry , Fluorescent Dyes/chemical synthesis , Fluorescent Dyes/toxicity , HEPES/chemistry , HeLa Cells/drug effects , Humans , Hydrogen-Ion Concentration , Magnetic Resonance Spectroscopy , Microscopy, Confocal , Molecular Structure , Permeability , Pyrazoles/chemistry , Sensitivity and Specificity , Spectrometry, Fluorescence , Spectrophotometry, Infrared , Sulfhydryl Compounds/chemistry
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