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Monoalkoxy BODIPYs--a fluorophore class for bioimaging.
- Source :
-
Bioconjugate chemistry [Bioconjug Chem] 2014 Jun 18; Vol. 25 (6), pp. 1043-51. Date of Electronic Publication: 2014 May 14. - Publication Year :
- 2014
-
Abstract
- Small molecule fluorophores are indispensable tools for modern biomedical imaging techniques. In this report, we present the development of a new class of BODIPY dyes based on an alkoxy-fluoro-boron-dipyrromethene core. These novel fluorescent dyes, which we term MayaFluors, are characterized by good aqueous solubility and favorable in vitro physicochemical properties. MayaFluors are readily accessible in good yields in a one-pot, two-step approach starting from well-established BODIPY dyes, and allow for facile modification with functional groups of relevance to bioconjugate chemistry and bioorthogonal labeling. Biological profiling in living cells demonstrates excellent membrane permeability, low nonspecific binding, and lack of cytotoxicity.
- Subjects :
- Boron Compounds chemical synthesis
Boron Compounds chemistry
Cell Membrane Permeability
Cell Survival
Female
Fluorescent Dyes chemical synthesis
Fluorescent Dyes chemistry
Humans
MCF-7 Cells
Molecular Structure
Solubility
Tumor Cells, Cultured
Boron Compounds analysis
Fluorescent Dyes analysis
Molecular Imaging methods
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4812
- Volume :
- 25
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Bioconjugate chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 24797834
- Full Text :
- https://doi.org/10.1021/bc400575w