• Title of article

    Synthesis and TNF-α inducing activities of mycoloyl-arabinan motif of mycobacterial cell wall components Original Research Article

  • Author/Authors

    Akihiro Ishiwata، نويسنده , , Hiroko Akao، نويسنده , , Yukishige Ito، نويسنده , , Makoto Sunagawa، نويسنده , , Naoto Kusunose، نويسنده , , Yasuo Kashiwazaki، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2006
  • Pages
    13
  • From page
    3049
  • To page
    3061
  • Abstract
    The extract of the cell wall skeleton of Bacillus Calmette–Guérin (BCG-CWS) from Mycobacterium bovis is known to be an activator of innate immunity. Synthesis of pentaarabinofuranoside as part of the arabinan moiety of BCG-CWS was achieved by double α-arabinofuranosylation followed by double β-arabinofuranosylation with orthogonally protected donors. Mycolic esters of the arabinan in the terminal lipo-arabinan motif of BCG-CWS were synthesized through alkylation of unprotected mycolic acid with bis- and tetra-tosylates of pentaarabinofuranoside. A series of compounds were subjected to a tumor necrosis factor alpha (TNF-α) secretion-inducing assay, disclosing aspects of the structure–activity relationship which should be useful in finding the site of the activity.
  • Keywords
    Stereoselective arabinofuranosylation , BCG-CWS , Mycoloyl-arabinan , TNF-? secretion-inducer
  • Journal title
    Bioorganic and Medicinal Chemistry
  • Serial Year
    2006
  • Journal title
    Bioorganic and Medicinal Chemistry
  • Record number

    1305675