Benzo[ g]coumarin-Based Fluorescent Probes for Bioimaging Applications

  • J Anal Methods Chem. 2018 Jun 14;2018:5249765. doi: 10.1155/2018/5249765.
Yuna Jung  1 Junyang Jung  1  2 Youngbuhm Huh  1  2 Dokyoung Kim  1  2  3
Affiliations
  • 1. Department of Biomedical Science, Graduate School, Kyung Hee University, 26 Kyungheedae-Ro, Dongdaemun-Gu, Seoul 02447, Republic of Korea.
  • 2. Department of Anatomy and Neurobiology, College of Medicine, Kyung Hee University, 26 Kyungheedae-Ro, Dongdaemun-Gu, Seoul 02447, Republic of Korea.
  • 3. Center for Converging Humanities, Kyung Hee University, 26 Kyungheedae-Ro, Dongdaemun-Gu, Seoul 02447, Republic of Korea.
Abstract

Benzo[g]Coumarins, which consist of Coumarins fused with Other aromatic units in the linear shape, have recently emerged as an interesting fluorophore in the bioimaging research. The pi-extended skeleton with the presence of electron-donating and electron-withdrawing substituents from the parent Coumarins changes the basic photophysical parameters such as absorption and fluorescence emission significantly. Most of the benzo[g]coumarin analogues show red/far-red fluorescence emission with high two-photon absorbing property that can be applicable for the two-photon microscopy (TPM) imaging. In this review, we summarized the recently developed benzo[g]coumarin analogues including photophysical properties, synthesis, and applications for molecular probes that can sense biologically important species such as metal ions, cell organs, reactive species, and disease biomarkers.

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