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
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
Journal title :
Bioorganic and Medicinal Chemistry