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Carbohydr Res ; 306(1-2): 163-70, 1998 Jan.
Article in English | MEDLINE | ID: mdl-9691445

ABSTRACT

Vibrio cholerae O1 LPS terminal mono- and disaccharide elements were synthesized by reduction of the azido group in several 4-amino-4,6-dideoxy-D-mannose mono- and disaccharide derivatives, followed by coupling with 2, 4-di-O-acetyl-3-deoxy-L-glycero-tetronic acid in the presence of 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline. This compound represents a useful model in order to elucidate the size of the epitopes which define Ogawa and Inaba serotypes from Vibrio cholerae O1.


Subject(s)
Antigens, Bacterial/chemistry , Disaccharides/chemical synthesis , Epitopes/chemistry , Hydroxybutyrates/chemical synthesis , Lipopolysaccharides/chemistry , Vibrio cholerae/immunology , Animals , Antibodies, Bacterial/immunology , Antigens, Bacterial/immunology , Carbohydrate Conformation , Disaccharides/chemistry , Disaccharides/immunology , Enzyme-Linked Immunosorbent Assay , Hydroxybutyrates/chemistry , Mice , Monosaccharides/chemical synthesis , Monosaccharides/chemistry , Monosaccharides/immunology , Optical Rotation , Serotyping , Vibrio cholerae/classification
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