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Monoalkoxy BODIPYs—A Fluorophore Class for Bioimaging

[Image: see text] 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 ch...

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Autores principales: Courtis, Alexandra M., Santos, Sofia A., Guan, Yinghua, Hendricks, J. Adam, Ghosh, Balaram, Szantai-Kis, D. Miklos, Reis, Surya A., Shah, Jagesh V., Mazitschek, Ralph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215867/
https://www.ncbi.nlm.nih.gov/pubmed/24797834
http://dx.doi.org/10.1021/bc400575w
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author Courtis, Alexandra M.
Santos, Sofia A.
Guan, Yinghua
Hendricks, J. Adam
Ghosh, Balaram
Szantai-Kis, D. Miklos
Reis, Surya A.
Shah, Jagesh V.
Mazitschek, Ralph
author_facet Courtis, Alexandra M.
Santos, Sofia A.
Guan, Yinghua
Hendricks, J. Adam
Ghosh, Balaram
Szantai-Kis, D. Miklos
Reis, Surya A.
Shah, Jagesh V.
Mazitschek, Ralph
author_sort Courtis, Alexandra M.
collection PubMed
description [Image: see text] 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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spelling pubmed-42158672015-05-05 Monoalkoxy BODIPYs—A Fluorophore Class for Bioimaging Courtis, Alexandra M. Santos, Sofia A. Guan, Yinghua Hendricks, J. Adam Ghosh, Balaram Szantai-Kis, D. Miklos Reis, Surya A. Shah, Jagesh V. Mazitschek, Ralph Bioconjug Chem [Image: see text] 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. American Chemical Society 2014-05-05 2014-06-18 /pmc/articles/PMC4215867/ /pubmed/24797834 http://dx.doi.org/10.1021/bc400575w Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Courtis, Alexandra M.
Santos, Sofia A.
Guan, Yinghua
Hendricks, J. Adam
Ghosh, Balaram
Szantai-Kis, D. Miklos
Reis, Surya A.
Shah, Jagesh V.
Mazitschek, Ralph
Monoalkoxy BODIPYs—A Fluorophore Class for Bioimaging
title Monoalkoxy BODIPYs—A Fluorophore Class for Bioimaging
title_full Monoalkoxy BODIPYs—A Fluorophore Class for Bioimaging
title_fullStr Monoalkoxy BODIPYs—A Fluorophore Class for Bioimaging
title_full_unstemmed Monoalkoxy BODIPYs—A Fluorophore Class for Bioimaging
title_short Monoalkoxy BODIPYs—A Fluorophore Class for Bioimaging
title_sort monoalkoxy bodipys—a fluorophore class for bioimaging
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215867/
https://www.ncbi.nlm.nih.gov/pubmed/24797834
http://dx.doi.org/10.1021/bc400575w
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