An azidoaryl thioglycoside of sialic acid. A potential photoaffinity probe of sialidases and sialic acid-binding proteins

Carbohydr Res. 1988 May 15;176(2):211-8. doi: 10.1016/0008-6215(88)80132-0.

Abstract

An azidoaryl thioglycoside of sialic acid was prepared, as a potential photoaffinity probe reagent for the analysis of sialidases and sialic acid-binding proteins, by treatment of the glycosyl chloride of N-acetylneuraminic acid methyl ester with potassium thioacetate to give, in 70% yield, methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-2-S-acetyl-2,3,5-trideoxy-2-thio-alph a-D- glycero-D-galacto-2-nonulopyranosonate. Selective hydrolysis of the thioacetate ester, followed by condensation with 4-fluoro-3-nitrophenyl azide, O-deacetylation, and hydrolysis gave (4-azido-2-nitrophenyl)- 5-acetamido-2,3,5-trideoxy-2-thio-alpha-D-glycero-D-galacto-2- nonulopyranosidonic acid.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Affinity Labels / chemical synthesis*
  • Azides / chemical synthesis*
  • Carrier Proteins / analysis*
  • Indicators and Reagents
  • Magnetic Resonance Spectroscopy
  • Neuraminidase / analysis*
  • Optical Rotation
  • Photochemistry
  • Sialic Acids / analysis*
  • Spectrophotometry, Infrared
  • Sugar Acids / chemical synthesis*

Substances

  • Affinity Labels
  • Azides
  • Carrier Proteins
  • Indicators and Reagents
  • Sialic Acids
  • Sugar Acids
  • (4-azido-2-nitrophenyl)-5-acetamido-2,3,5-trideoxy-2-thioglycerogalacto-2-nonulopyranosidonic acid
  • Neuraminidase