Publication | Closed Access
Structurally Rigid 9-Amino-benzo[<i>c</i>]cinnoliniums Make Up a Class of Compact and Large Stokes-Shift Fluorescent Dyes for Cell-Based Imaging Applications
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Citations
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References
2015
Year
EngineeringRigid 9-Amino-benzoBioimagingThermally Activated Delayed FluorescencePhotophysical PropertyMolecular ImagingBiophysicsNovel Imaging MethodLarge Stokes ShiftBiochemistryFluorescence ImagingBiological StudiesClassic Fluorescent DyesCell-based Imaging ApplicationsSingle-molecule DetectionBiomolecular EngineeringBiomedical ImagingMolecular SwitchChemical Probe
Classic fluorescent dyes, such as coumarin, naphthalimide, fluorescein, BODIPY, rhodamine, and cyanines, are cornerstones of various spectroscopic and microscopic methods, which hold a prominent position in biological studies. We recently found that 9-amino-benzo[c]cinnoliniums make up a novel group of fluorophores that can be used in biological studies. They are featured with a succinct conjugative push-pull backbone, a broad absorption band, and a large Stokes shift. They are potentially useful as a small-molecule alternative to R-phycoerythrin to pair with fluorescein in multiplexing applications.
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