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Monoalkoxy BODIPYs—A Fluorophore Class for Bioimaging
Author(s) -
Alexandra M. Courtis,
Sofia A. Santos,
Yinghua Guan,
J. Adam Hendricks,
Balaram Ghosh,
D. Miklos SzantaiKis,
Surya A. Reis,
Jagesh V. Shah,
Ralph Mazitschek
Publication year - 2014
Publication title -
bioconjugate chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.279
H-Index - 172
eISSN - 1520-4812
pISSN - 1043-1802
DOI - 10.1021/bc400575w
Subject(s) - chemistry , bodipy , fluorophore , bioconjugation , bioorthogonal chemistry , combinatorial chemistry , fluorescence , membrane permeability , nanotechnology , click chemistry , biophysics , membrane , biochemistry , physics , materials science , quantum mechanics , biology
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.

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