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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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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. |
format | Online Article Text |
id | pubmed-4215867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
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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