Title of article :
Synthesis and NMR studies on the ABO histo-blood group antigens: synthesis of type III and IV structures and NMR characterization of type I–VI antigens Original Research Article
Author/Authors :
Peter J. Meloncelli، نويسنده , , Lori J. West، نويسنده , , Todd L. Lowary، نويسنده ,
Issue Information :
دوهفته نامه با شماره پیاپی سال 2011
Pages :
21
From page :
1406
To page :
1426
Abstract :
The ABO histo-blood group antigens are best known for their important roles in solid organ and bone marrow transplantation as well as transfusion medicine. Here we report the synthesis of the ABO type III and IV antigens with a 7-octen-1-yl aglycone. Also described is an NMR study of the ABO type I to VI antigens, which were carried out to probe differences in overall conformation of the molecules. These NMR investigations showed very little difference in the 1H chemical shifts, as well as 1H–1H coupling constants, across all compounds, suggesting that these ABO subtypes adopt nearly identical conformations in solution.
Keywords :
ABO histo-blood group , ABO type IV , Chemical synthesis , Trichloroacetimidate , ABO type III , 7-Octen-1-yl
Journal title :
Carbohydrate Research
Serial Year :
2011
Journal title :
Carbohydrate Research
Record number :
967202
Link To Document :
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