Synthesis and carbohydrate binding studies of fluorescent alpha-amidoboronic acids and the corresponding bisboronic acids

Bioorg Med Chem. 2010 Feb 15;18(4):1449-55. doi: 10.1016/j.bmc.2010.01.017. Epub 2010 Jan 11.

Abstract

Fluorescent boronic acids are very useful for the design and synthesis of carbohydrate sensors. In an earlier communication, we first described the effort of developing water soluble fluorescent alpha-amidoboronic acids, which change fluorescence upon sugar binding. In this report, we describe a general method of functionalizing such boronic acids and their applications in the preparation of bis-alpha-amidoboronic acids with significantly enhanced binding for oligosaccharides as compared to their monoboronic acid counterparts. The advantages of good water solubility, easy modification to generate diversity, and modularity in synthesis will make alpha-amidoboronic acids very useful building blocks for future synthesis of boronic acid-based fluorescent sensors.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Boronic Acids / chemical synthesis*
  • Boronic Acids / chemistry
  • Carbohydrates / chemistry*
  • Chromatography, High Pressure Liquid
  • Magnetic Resonance Spectroscopy
  • Models, Molecular
  • Spectrometry, Mass, Electrospray Ionization
  • Spectrophotometry, Ultraviolet

Substances

  • Boronic Acids
  • Carbohydrates