A BODIPY-based ‘turn-on’ fluorescent probe for hypoxic cell imaging
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Title
A BODIPY-based ‘turn-on’ fluorescent probe for hypoxic cell imaging
Authors
Keywords
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Journal
CHEMICAL COMMUNICATIONS
Volume 51, Issue 69, Pages 13389-13392
Publisher
Royal Society of Chemistry (RSC)
Online
2015-07-14
DOI
10.1039/c5cc05139h
References
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Note: Only part of the references are listed.- Structural modification strategies for the rational design of red/NIR region BODIPYs
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- (2013) Lizhi Gai et al. CHEMISTRY-A EUROPEAN JOURNAL
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- A New Prodrug-Derived Ratiometric Fluorescent Probe for Hypoxia: High Selectivity of Nitroreductase and Imaging in Tumor Cell
- (2011) Lei Cui et al. ORGANIC LETTERS
- Specific Cu2+-induced J-aggregation and Hg2+-induced fluorescence enhancement based on BODIPY
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- Indolequinone-rhodol conjugate as a fluorescent probe for hypoxic cells: enzymatic activation and fluorescence properties
- (2010) Hirokazu Komatsu et al. MedChemComm
- Design of a bioreductively-activated fluorescent pH probe for tumor hypoxia imaging
- (2009) Eiji Nakata et al. BIOORGANIC & MEDICINAL CHEMISTRY
- Increasing Sensitivity to Radiotherapy and Chemotherapy by Using Novel Biological Agents that Alter the Tumor Microenvironment
- (2009) E. Shinohara et al. CURRENT MOLECULAR MEDICINE
- Red/Near-infrared Boron-Dipyrromethene Dyes as Strongly Emitting Fluorophores
- (2008) Ana B. Descalzo et al. Annals of the New York Academy of Sciences
- The Chemistry of Fluorescent Bodipy Dyes: Versatility Unsurpassed
- (2007) Gilles Ulrich et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
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