1355953-56-8Relevant articles and documents
Rational design of fluorescent probes for targeted: In vivo nitroreductase visualization
Chen, Ji-An,Gao, Jie,Gu, Xianfeng,Li, Mimi,Tan, Jiahui,Yin, Xiaofan,Zhao, Zhen
, p. 4744 - 4747 (2020)
Nitroreductase (NTR) has been recognized as a biomarker for identifying the hypoxic status of cancers. Therefore, it is of high scientific interest to design effective fluorescent probes for tracking NTR activity. However, studies on elucidation of the structure-performance relationship of fluorescent probes and those providing valuable insight into optimized probe design have rarely been reported. Three BODIPY based fluorescent probes were made by conjugation of para-, ortho-, and meta-nitrobenzene to the BODIPY core via a thiolether bond, respectively. Our study revealed that the linkage and nitro substituent position significantly influence the capability of nitroreductase detection.
Design, synthesis and photophysical studies of BODIPY-o, m, p-phenylenediamine-based probes: Insights into their responsiveness under different pH conditions
Jin, Guofan,Li, Binxian,Xiao, Fuyan,Zhao, Wantao
, (2021)
In this paper, a series of novel phenylenediamine-fluoroboron pyrrole fluorescent derivatives were prepared which have distinct responsiveness under different hydrogen ion concentration (pH) conditions. It is noticed that the products showed excellent flu
BODIPY-based sulfoxide: Synthesis, photophysical characterization and response to benzenethiols
Zhao, Chunchang,Wang, Xuzhe,Cao, Jian,Feng, Peng,Zhang, Jinxin,Zhang, Yanfen,Yang, Yang,Yang, Zhenjun
, p. 328 - 332 (2013/02/22)
Two BODIPY dyes bearing a sulfur containing function at the 3-position are reported. The 3-benzylthio compound shows spectroscopic features of the classical BODIPY platform, showing minor solvent dependent spectral shift, a relative small Stokes shift and
Development of a borondipyrromethene-based Zn2+ fluorescent probe: Solvent effects on modulation sensing ability
Zhao, Chunchang,Zhang, Yulin,Feng, Peng,Cao, Jian
experimental part, p. 831 - 838 (2012/03/07)
A borondipyrromethene-based Zn2+ fluorescent probe BODPAQ was designed and synthesized. The chelators in BODPAQ, 2,2′-dipicolylamine (DPA) and 8-aminoquinoline (AQ), coordinate to Zn2+ in a synergic manner. As a result, BODPAQ displa