Chem. J. Chinese Universities ›› 2009, Vol. 30 ›› Issue (11): 2199.

• Articles • Previous Articles     Next Articles

Highly Efficient Synthesis of Two Hyaluronan Trisaccharide Analogues for Potential Hyaluronic Acid Synthases Inhibitors

WEI Guo-Hua1,2*, DU Yu-Guo1, Khushi L. Matta2   

  1. 1. State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China;
    2. Cancer Biology, Roswell Park Cancer Institute, Buffalo, NY 14263, USA
  • Received:2009-03-06 Online:2009-11-10 Published:2009-11-10
  • Contact: WEI Guo-Hua. E-mail: wgh@rcees.ac.cn
  • Supported by:

    国家自然科学基金(批准号: 30701043)资助.

Abstract:

The syntheses of two hyaluronan trisaccharide analogues, naphthyl O-(3-methoxy-β-D-glucopy-ranosyluronic acid)-(1,3)-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1,4)-O-β-D-glucopyranosyluronic acid and naphthyl O-(3-methoxy-2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1,4)-O-(β-D-glucopyranosyluronic acid)-(1,3)-O-2-acetamido-2-deoxy-β-D-glucopyranoside, were described. Construction of the target molecules was achieved through a combination of BF3·Et2O/toluene system and trichloroacetimidate glycosylation methodology. This is the first report on the synthesis of the 3-methoxyl derivatives, which represent the smallest fragments that incorporate all the structural features of polymeric hyaluronan and can be used for potential hyaluronic acid synthases inhibitors.

Key words: Hyaluronan; Hyaluronic acid synthase; Inhibitor; 2-Naphthylmethyl(NAP)

TrendMD: