Literature DB >> 21381720

4,4-Difluoro-4-bora-3a,4a-diaza-s-indacene as a bright fluorescent label for DNA.

Thomas Ehrenschwender1, Hans-Achim Wagenknecht.   

Abstract

4,4-Difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) as a fluorescent label can be incorporated into DNA by two conceptually different ways: the non-nucleosidic DNA base surrogate Bo exhibits high brightness but no preferential base-pairing properties, whereas the BODIPY-modified uridine BodU has reduced quantum yields but shows preferred Watson-Crick base pairing with adenine.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21381720     DOI: 10.1021/jo102519k

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

1.  Synthesis, spectroscopic, and in vitro investigations of 2,6-diiodo-BODIPYs with PDT and bioimaging applications.

Authors:  Jaime H Gibbs; Zehua Zhou; David Kessel; Frank R Fronczek; Svetlana Pakhomova; M Graça H Vicente
Journal:  J Photochem Photobiol B       Date:  2015-02-27       Impact factor: 6.252

2.  Synthesis of Wavelength-Shifting Fluorescent DNA and RNA with Two Photostable Cyanine-Styryl Dyes as the Base Surrogate Pair.

Authors:  Jeannine Steinmeyer; Franziska Rönicke; Ute Schepers; Hans-Achim Wagenknecht
Journal:  ChemistryOpen       Date:  2017-06-07       Impact factor: 2.911

3.  Green-Light Activatable BODIPY and Coumarin 5'-Caps for Oligonucleotide Photocaging.

Authors:  Janik Kaufmann; Patricia Müller; Eleni Andreadou; Alexander Heckel
Journal:  Chemistry       Date:  2022-05-17       Impact factor: 5.020

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.