4.3 Article

Fluorescent-Oxaboroles: Synthesis and Optical Property by Sugar Recognition

Journal

CHEMICAL & PHARMACEUTICAL BULLETIN
Volume 69, Issue 6, Pages 526-528

Publisher

PHARMACEUTICAL SOC JAPAN
DOI: 10.1248/cpb.c21-00179

Keywords

oxaborole; recognition; nucleic acid; photo quenching

Funding

  1. Kanazawa University SAKIGAKE project 2018
  2. Kanazawa University SAKIGAKE project 2020
  3. Takeda Science Foundation

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The optical properties of fluorescent unit-conjugated aliphatic oxaboroles have been studied, showing good fluorescence quantum yields and selective recognition of D-ribose and D-ribose containing molecules. Molecular recognition led to significant fluorescence quenching, suggesting the potential for a boron-based NAD sensor probe.
The optical property of fluorescent unit-conjugated aliphatic oxaboroles has been investigated. The oxaboroles provide good fluorescence quantum yields and selective recognition toward D-ribose and D-ribose containing molecules. The molecular recognition induced significant fluorescence quenching. The property of the boroles showed the possibility of the boron-based nicotinamide adenine dinucleotide (NAD) sensor probe.

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